Human (GRCh38.p14)
Description

bone morphogenetic protein receptor type 1A [Source:HGNC Symbol;Acc:HGNC:1076]

Gene Synonyms

ACVRLK3, ALK3, CD292

Location
About this transcript

This transcript has 13 exons, is annotated with 41 domains and features, is associated with 77754 variant alleles and maps to 883 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000372037.8BMPR1A-2016417532aaENSP00000361107.2
 
Protein coding
CCDS7378P36894 NM_004329.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000480152.3BMPR1A-2026347532aaENSP00000483569.2
 
Protein coding
CCDS7378A0A087X0P8 -GENCODE basicAPPRIS P1TSL:3
ENST00000638429.1BMPR1A-2055632532aaENSP00000492290.1
 
Nonsense mediated decay
CCDS7378P36894 -TSL:5
ENST00000635816.2BMPR1A-2034885532aaENSP00000489707.1
 
Nonsense mediated decay
CCDS7378P36894 -TSL:5
ENST00000636056.2BMPR1A-2043558532aaENSP00000490273.1
 
Nonsense mediated decay
CCDS7378P36894 -TSL:5
Statistics

Exons: 13, Coding exons: 11, Transcript length: 6,417 bps, Translation length: 532 residues

MANE

This MANE Select transcript contains ENSP00000361107 and matches to NM_004329.3 and NP_004320.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P36894

CCDS

This transcript is a member of the Human CCDS set: CCDS7378

Transcript Support Level (TSL)

TSL:1

Version

ENST00000372037.8

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.