Human (GRCh38.p14)
Description

synaptotagmin 9 [Source:HGNC Symbol;Acc:HGNC:19265]

Location
About this transcript

This transcript has 7 exons, is annotated with 24 domains and features, is associated with 92266 variant alleles and maps to 362 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000318881.11SYT9-2014002491aaENSP00000324419.6
 
Protein coding
CCDS7778Q86SS6 NM_175733.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000532592.1SYT9-2033183173aaENSP00000434558.1
 
Nonsense mediated decay
B3KNT7 -TSL:2
ENST00000524820.6SYT9-2022094319aaENSP00000432141.2
 
Nonsense mediated decay
E9PDN4 -TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 4,002 bps, Translation length: 491 residues

MANE

This MANE Select transcript contains ENSP00000324419 and matches to NM_175733.4 and NP_783860.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q86SS6

CCDS

This transcript is a member of the Human CCDS set: CCDS7778

Transcript Support Level (TSL)

TSL:1

Version

ENST00000318881.11

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.