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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS5397.1 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
5397.1 |
Public |
Homo sapiens |
7 |
HNRNPA2B1 |
24 |
110 |
108 |
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Public since: CCDS release 1, NCBI annotation release 35.1, Ensembl annotation release 23
Review status: Reviewed (by RefSeq and Havana) Sequence IDs included in CCDS 5397.1
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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EBI |
ENST00000618183.5 |
ENSP00000478691.2 |
MANE Select |
Accepted |
alive |
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EBI |
ENST00000608362.2 |
ENSP00000497298.1 |
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Accepted |
alive |
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EBI |
ENST00000677574.1 |
ENSP00000503021.1 |
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Accepted |
alive |
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EBI |
ENST00000678697.1 |
ENSP00000503047.1 |
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Accepted |
alive |
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EBI |
ENST00000677656.1 |
ENSP00000503060.1 |
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Accepted |
alive |
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EBI |
ENST00000677339.1 |
ENSP00000503242.1 |
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Accepted |
alive |
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EBI |
ENST00000678449.1 |
ENSP00000503375.1 |
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Accepted |
alive |
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EBI |
ENST00000678779.1 |
ENSP00000503429.1 |
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Accepted |
alive |
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EBI |
ENST00000677631.1 |
ENSP00000503452.1 |
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Accepted |
alive |
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EBI |
ENST00000678998.1 |
ENSP00000503460.1 |
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Accepted |
alive |
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EBI |
ENST00000678884.1 |
ENSP00000503501.1 |
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Accepted |
alive |
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EBI |
ENST00000677396.1 |
ENSP00000503703.1 |
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Accepted |
alive |
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EBI |
ENST00000678431.1 |
ENSP00000503833.1 |
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Accepted |
alive |
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EBI |
ENST00000676497.1 |
ENSP00000503836.1 |
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Accepted |
alive |
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EBI |
ENST00000677906.1 |
ENSP00000503870.1 |
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Accepted |
alive |
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EBI |
ENST00000678501.1 |
ENSP00000503961.1 |
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Accepted |
alive |
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EBI |
ENST00000678935.1 |
ENSP00000504023.1 |
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Accepted |
alive |
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EBI |
ENST00000679243.1 |
ENSP00000504415.1 |
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Accepted |
alive |
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EBI |
ENST00000677839.1 |
ENSP00000504439.1 |
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Accepted |
alive |
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EBI |
ENST00000679318.1 |
ENSP00000504571.1 |
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Accepted |
alive |
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EBI |
ENST00000676903.1 |
ENSP00000504660.1 |
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Accepted |
alive |
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EBI |
ENST00000678962.1 |
ENSP00000504721.1 |
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Accepted |
alive |
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EBI |
ENST00000676749.1 |
ENSP00000504799.1 |
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Accepted |
alive |
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EBI |
ENST00000676524.1 |
ENSP00000504831.1 |
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Accepted |
alive |
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NCBI |
NM_002137.4 |
NP_002128.1 |
MANE Select |
Accepted |
alive |
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RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_002128.1 |
341 |
P22626-2 |
341 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 5397.1
Assembly GRCh38.p14 (GCF_000001405.40)
CCDS Sequence Data |
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Blue highlighting indicates alternating exons. | Red highlighting indicates amino acids encoded across a splice junction. | | Mouse over the nucleotide or protein sequence below and click on the highlighted codon or residue to select the pair. |
Nucleotide Sequence (1026 nt): ATGGAGAGAGAAAAGGAACAGTTCCGTAAGCTCTTTATTGGTGGCTTAAGCTTTGAAACCACAGAAGAAA GTTTGAGGAACTACTACGAACAATGGGGAAAGCTTACAGACTGTGTGGTAATGAGGGATCCTGCAAGCAA AAGATCAAGAGGATTTGGTTTTGTAACTTTTTCATCCATGGCTGAGGTTGATGCTGCCATGGCTGCAAGA CCTCATTCAATTGATGGGAGAGTAGTTGAGCCAAAACGTGCTGTAGCAAGAGAGGAATCTGGAAAACCAG GGGCTCATGTAACTGTGAAGAAGCTGTTTGTTGGCGGAATTAAAGAAGATACTGAGGAACATCACCTTAG AGATTACTTTGAGGAATATGGAAAAATTGATACCATTGAGATAATTACTGATAGGCAGTCTGGAAAGAAA AGAGGCTTTGGCTTTGTTACTTTTGATGACCATGATCCTGTGGATAAAATCGTATTGCAGAAATACCATA CCATCAATGGTCATAATGCAGAAGTAAGAAAGGCTTTGTCTAGACAAGAAATGCAGGAAGTTCAGAGTTC TAGGAGTGGAAGAGGAGGCAACTTTGGCTTTGGGGATTCACGTGGTGGCGGTGGAAATTTCGGACCAGGA CCAGGAAGTAACTTTAGAGGAGGATCTGATGGATATGGCAGTGGACGTGGATTTGGGGATGGCTATAATG GGTATGGAGGAGGACCTGGAGGTGGCAATTTTGGAGGTAGCCCCGGTTATGGAGGAGGAAGAGGAGGATA TGGTGGTGGAGGACCTGGATATGGCAACCAGGGTGGGGGCTACGGAGGTGGTTATGACAACTATGGAGGA GGAAATTATGGAAGTGGAAATTACAATGATTTTGGAAATTATAACCAGCAACCTTCTAACTACGGTCCAA TGAAGAGTGGAAACTTTGGTGGTAGCAGGAACATGGGGGGACCATATGGTGGAGGAAACTATGGTCCAGG AGGCAGTGGAGGAAGTGGGGGTTATGGTGGGAGGAGCCGATACTGA
Translation (341 aa): MEREKEQFRKLFIGGLSFETTEESLRNYYEQWGKLTDCVVMRDPASKRSRGFGFVTFSSMAEVDAAMAAR PHSIDGRVVEPKRAVAREESGKPGAHVTVKKLFVGGIKEDTEEHHLRDYFEEYGKIDTIEIITDRQSGKK RGFGFVTFDDHDPVDKIVLQKYHTINGHNAEVRKALSRQEMQEVQSSRSGRGGNFGFGDSRGGGGNFGPG PGSNFRGGSDGYGSGRGFGDGYNGYGGGPGGGNFGGSPGYGGGRGGYGGGGPGYGNQGGGYGGGYDNYGG GNYGSGNYNDFGNYNQQPSNYGPMKSGNFGGSRNMGGPYGGGNYGPGGSGGSGGYGGRSRY
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