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Human (GRCh38.p14)
Description

synaptotagmin 13 [Source:HGNC Symbol;Acc:HGNC:14962]

Gene Synonyms

KIAA1427

Location
About this transcript

This transcript has 6 exons, is annotated with 22 domains and features, is associated with 19540 variant alleles and maps to 321 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000020926.8SYT13-2015165426aaENSP00000020926.3
 
Protein coding
CCDS31470Q7L8C5 NM_020826.3MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00001139951.1SYT13-2045171426aaENSP00000801247.1
 
Protein coding
CCDS31470--Ensembl Canonical ExtendedGENCODE BasicAPPRIS P1
ENST00000528101.1SYT13-202557186aaENSP00000432975.1
 
Protein coding
H0YD47 -TSL:4CDS 5' and 3' incomplete
ENST00000533332.1SYT13-203171020aaENSP00000434967.1
 
Nonsense mediated decay
H0YE47 -TSL:1CDS 5' incomplete
Statistics

Exons: 6, Coding exons: 6, Transcript length: 5,165 bps, Translation length: 426 residues

MANE

This MANE Select transcript contains ENSP00000020926 and matches to NM_020826.3 and NP_065877.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q7L8C5

CCDS

This transcript is a member of the Human CCDS set: CCDS31470

Transcript Support Level (TSL)

TSL:1

Version

ENST00000020926.8

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.