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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
Genomic
-
NG_032138.1 RefSeqGene
- Range
-
5001..26877
- Download
- GenBank, FASTA, Sequence Viewer (Graphics), LRG_414
mRNA and Protein(s)
-
NM_001256891.2 → NP_001243820.1 sorcin isoform C
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) differs in the 3' coding region and 3' UTR, compared to variant 1. These differences result in a protein (isoform C) with a shorter and distinct C-terminus, compared to isoform A.
- Source sequence(s)
-
AC005075, AK296601, BI524104, DA268050
- UniProtKB/Swiss-Prot
-
P30626
- Conserved Domains (1) summary
-
- cd00051
Location:75 → 130
- EFh; EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to ...
-
NM_001256892.2 → NP_001243821.1 sorcin isoform D
See identical proteins and their annotated locations for NP_001243821.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (4) has multiple differences compared to variant 1. These differences result in a protein (isoform D) with shorter and distinct N- and C-termini, compared to isoform A.
- Source sequence(s)
-
AC005075, AK296601
- Consensus CDS
-
CCDS59063.1
- UniProtKB/TrEMBL
-
C9J0K6
- Related
- ENSP00000391148.1, ENST00000431660.5
- Conserved Domains (1) summary
-
- cd16187
Location:19 → 175
- EFh_PEF_sorcin; Penta-EF hand, calcium binding motifs, found in sorcin
-
NM_003130.4 → NP_003121.1 sorcin isoform A
See identical proteins and their annotated locations for NP_003121.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (A).
- Source sequence(s)
-
AC005075, AK129770, AK295225, AL117616, DA268050, DB540255
- Consensus CDS
-
CCDS5612.1
- UniProtKB/Swiss-Prot
- A8MTH6, B4DKK2, D6W5Q0, P30626
- Related
- ENSP00000265729.3, ENST00000265729.7
- Conserved Domains (1) summary
-
- cd16187
Location:34 → 198
- EFh_PEF_sorcin; Penta-EF hand, calcium binding motifs, found in sorcin
-
NM_198901.2 → NP_944490.1 sorcin isoform B
See identical proteins and their annotated locations for NP_944490.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (2) differs in the 5' UTR and coding region and uses an alternate translational start codon, compared to variant 1. These differences result in a protein (isoform B) with a shorter and distinct N-terminus, compared to isoform A.
- Source sequence(s)
-
AC005075, AL117616, AL576812, BM739144, BM793972
- Consensus CDS
-
CCDS47638.1
- UniProtKB/TrEMBL
-
C9J0K6
- Related
- ENSP00000378137.3, ENST00000394641.7
- Conserved Domains (1) summary
-
- cd16187
Location:19 → 183
- EFh_PEF_sorcin; Penta-EF hand, calcium binding motifs, found in sorcin
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000007.14 Reference GRCh38.p14 Primary Assembly
- Range
-
88205115..88226976 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060931.1 Alternate T2T-CHM13v2.0
- Range
-
89455604..89477464 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)