Human (GRCh38.p14)
Description

vinculin [Source:HGNC Symbol;Acc:HGNC:12665]

Location
About this transcript

This transcript has 22 exons, is annotated with 93 domains and features, is associated with 47541 variant alleles and maps to 797 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000211998.10VCL-20154971134aaENSP00000211998.5
 
Protein coding
CCDS7341P18206-1 NM_014000.3MANE SelectEnsembl CanonicalGENCODE basicTSL:1
ENST00000372755.7VCL-20264891066aaENSP00000361841.3
 
Protein coding
CCDS7340P18206-2 -GENCODE basicAPPRIS P1TSL:1
ENST00000624354.3VCL-207330757aaENSP00000485551.1
 
Nonsense mediated decay
A0A096LPE1 -TSL:2
ENST00000623461.3VCL-2067995No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000478896.2VCL-205727No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000461383.1VCL-203268No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000472585.1VCL-204556No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 22, Coding exons: 22, Transcript length: 5,497 bps, Translation length: 1,134 residues

MANE

This MANE Select transcript contains ENSP00000211998 and matches to NM_014000.3 and NP_054706.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: P18206

CCDS

This transcript is a member of the Human CCDS set: CCDS7341

Transcript Support Level (TSL)

TSL:1

Version

ENST00000211998.10

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.