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Genome Displays Related Resources Gene HomoloGene MANE RefSeq
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Report for CCDS41621.1 (current version)
CCDS |
Status |
Species |
Chrom. |
Gene |
CCDS Release |
NCBI Annotation Release |
Ensembl Annotation Release |
Links |
41621.1 |
Public |
Homo sapiens |
11 |
INSC |
24 |
110 |
108 |
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Public since: CCDS release 5, NCBI annotation release 36.3, Ensembl annotation release 47
Review status: Reviewed (by RefSeq and Havana) Sequence IDs included in CCDS 41621.1
Original |
Current |
Source |
Nucleotide ID |
Protein ID |
MANE |
Status in CCDS |
Seq. Status |
Links |
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EBI |
ENST00000379554.7 |
ENSP00000368872.3 |
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Accepted |
alive |
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NCBI |
NM_001031853.5 |
NP_001027024.3 |
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Accepted |
alive |
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RefSeq |
Length |
Related UniProtKB/SwissProt |
Length |
Identity |
Gaps |
Mismatches |
NP_001027024.3 |
579 |
Q1MX18-1 |
579 |
100% |
0 |
0 |
Chromosomal Locations for CCDS 41621.1
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 (1740 nt): ATGAGACGGCCCCCTGGCAATGGAGAGGCGGCCAGCGAAGGTCCAGGTGGCTGGGGTCTATGGGGAGTCC AGGAGTCCAGGAGGCTGTGCTGTGCCGGTCACGACCGCTGCAAGCAGGCTTTGCTGCAGATTGGGATCAA CATGATGGCACTGCCTGGAGGTCGCCACCTGGACTCCGTCACCCTGCCGGGTCAGCGGCTACACCTGATG CAGGTGGACTCAGTCCAGCGCTGGATGGAAGATCTGAAGCTCATGACCGAGTGCGAGTGCATGTGTGTCC TGCAGGCCAAGCCCATCAGCCTGGAAGAGGATGCACAGGGTGACCTCATCCTGGCAGGTGGCCCTGGCCC TGGAGACCCCCTGCAGCTGCTGCTCAAACGGGGTTGGGTCATTAGCACAGAGCTGCGCAGGATCGGGCAG AAGCTGGCCCAGGACCGCTGGGCACGGGTGCACAGCATGAGCGTGCGTCTGACCTGCCATGCCCGCTCCA TGGTCAGCGAGTACAGTGCTGTCAGCAGGAACTCCTTGAAGGAAATGGGCGAGATTGAGAAGCTGCTAAT GGAGAAATGCTCGGAGCTCTCGGCAGTCACAGAGAGGTGCCTTCAGGTTGAGAATGAGCATGTCCTGAAG TCAATGAAGGCCTGCGTGAGTGAGACCCTGAGCATGCTGGGCCAGCACTTTGGTCAGCTGCTGGAGCTGG CCCTGACACGGGAGGTTCAGGCACTGGTGAGAAAAATTGATGCCTCAGACAATATCTACACCACAGAGTC CACCACAGGGAACCTGTTCAGCCTGACCCAGGAGGGGGCTCCCTTGTGCCGCATCATAGCCAAGGAGGGT GGGGTCGTAGCACTCTTCAAGGTTTGCCGGCAGGACAGTTTCCGGTGCTTGTACCCCCAGGCGCTCCGCA CGCTGGCCTCCATCTGCTGCGTGGAAGAGGGTGTCCACCAGCTGGAGAAGGTGGATGGCGTTCTGTGCTT GGCCGACATCCTGACCGACAACAGCCACTCAGAGGCCACACGGGCTGAGGCTGCGGCTGTGGTGGCCCAG GTCACCTCCCCACACCTGCCCGTCACCCAGCACCTCAGTAGCTTCCTGGAGAGCATGGAGGAGATCGTGA CAGCCCTCGTCAAACTGTGCCAAGAGGCCTCATCAGGGGAAGTCTTCCTACTGGCCTCTGCGGCCCTTGC CAACATCACGTTCTTTGACACAATGGCCTGCGAGATGCTCCTGCAGTTGAATGCCATCCGTGTTCTCCTG GAAGCCTGCAGTGACAAGCAGAGAGTGGACACGCCTTACACTCGGGACCAGATTGTGACCATCTTGGCAA ACATGTCTGTCCTAGAACAGTGTGCCTCTGACATCATTCAGGAAAATGGGGTCCAGCTTATCATGGGCAT GCTGTCTGAAAAACCAAGGTCTGGGACTCCTGCTGAAGTGGCAGCCTGTGAGCGAGTCCAGCAGAAAGCT GCAGTGACCCTGGCTCGTCTCAGCCGAGACCCAGATGTGGCACGGGAGGCCGTGCGGCTCAGCTGCATGT CCCGTCTCATCGAGCTCTGCAGATCCCCATCAGAGAGGAACAGCAGTGACGCCGTGCTTGTGGCCTGCCT GGCTGCTCTGCGTAGATTGGCTGGGGTCTGCCCTGAAGGCCTCCAGGACTCTGACTTTCAGCAGTTGGTC CAGCCTCGGCTGGTGGACTCCTTCTTACTCTGCAGCAACATGGAGGAGAGTTTTGTGTAG
Translation (579 aa): MRRPPGNGEAASEGPGGWGLWGVQESRRLCCAGHDRCKQALLQIGINMMALPGGRHLDSVTLPGQRLHLM QVDSVQRWMEDLKLMTECECMCVLQAKPISLEEDAQGDLILAGGPGPGDPLQLLLKRGWVISTELRRIGQ KLAQDRWARVHSMSVRLTCHARSMVSEYSAVSRNSLKEMGEIEKLLMEKCSELSAVTERCLQVENEHVLK SMKACVSETLSMLGQHFGQLLELALTREVQALVRKIDASDNIYTTESTTGNLFSLTQEGAPLCRIIAKEG GVVALFKVCRQDSFRCLYPQALRTLASICCVEEGVHQLEKVDGVLCLADILTDNSHSEATRAEAAAVVAQ VTSPHLPVTQHLSSFLESMEEIVTALVKLCQEASSGEVFLLASAALANITFFDTMACEMLLQLNAIRVLL EACSDKQRVDTPYTRDQIVTILANMSVLEQCASDIIQENGVQLIMGMLSEKPRSGTPAEVAACERVQQKA AVTLARLSRDPDVAREAVRLSCMSRLIELCRSPSERNSSDAVLVACLAALRRLAGVCPEGLQDSDFQQLV QPRLVDSFLLCSNMEESFV
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