Human (GRCh38.p14)
Description

integrin subunit alpha 11 [Source:HGNC Symbol;Acc:HGNC:6136]

Gene Synonyms

HST18964

Location
About this transcript

This transcript has 30 exons, is annotated with 46 domains and features, is associated with 62703 variant alleles and maps to 1018 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000315757.9ITGA11-201101911188aaENSP00000327290.7
 
Protein coding
CCDS45291Q9UKX5-1 NM_001004439.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000423218.6ITGA11-202101921189aaENSP00000403392.2
 
Protein coding
Q9UKX5-2 -GENCODE basicAPPRIS ALT1TSL:2
ENST00000562826.5ITGA11-203670No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000566429.1ITGA11-205567No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000569346.5ITGA11-207783No protein-
 
Retained intron
--TSL:4
ENST00000568677.1ITGA11-206651No protein-
 
Retained intron
--TSL:3
ENST00000565868.5ITGA11-204401No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 30, Coding exons: 30, Transcript length: 10,191 bps, Translation length: 1,188 residues

MANE

This MANE Select transcript contains ENSP00000327290 and matches to NM_001004439.2 and NP_001004439.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UKX5

CCDS

This transcript is a member of the Human CCDS set: CCDS45291

Transcript Support Level (TSL)

TSL:1

Version

ENST00000315757.9

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.