Human (GRCh38.p14)
Description

synaptotagmin 2 [Source:HGNC Symbol;Acc:HGNC:11510]

About this transcript

This transcript has 9 exons, is annotated with 34 domains and features, is associated with 51697 variant alleles and maps to 478 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367268.5SYT2-2027635419aaENSP00000356237.4
 
Protein coding
CCDS1427Q8N9I0 NM_177402.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P3TSL:1
ENST00000367267.5SYT2-2017614419aaENSP00000356236.1
 
Protein coding
CCDS1427Q8N9I0 -GENCODE BasicAPPRIS P3TSL:2
ENST00000930882.1SYT2-2053226422aaENSP00000600941.1
 
Protein coding
--GENCODE BasicAPPRIS ALT1
ENST00000930883.1SYT2-2062652439aaENSP00000600942.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000899895.1SYT2-2032447422aaENSP00000569954.1
 
Protein coding
--GENCODE BasicAPPRIS ALT1
ENST00000899896.1SYT2-2042283422aaENSP00000569955.1
 
Protein coding
--GENCODE BasicAPPRIS ALT1
Statistics

Exons: 9, Coding exons: 8, Transcript length: 7,635 bps, Translation length: 419 residues

MANE

This MANE Select transcript contains ENSP00000356237 and matches to NM_177402.5 and NP_796376.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8N9I0

CCDS

This transcript is a member of the Human CCDS set: CCDS1427

Transcript Support Level (TSL)

TSL:1

Version

ENST00000367268.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.