Canonical Allele Identifier: CA7191839
Gene: BMP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2381876
ClinVar RCV Id: RCV002674694
dbSNP Id: rs759558138

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53952135T>C , CM000676.2:g.53952135T>C GRCh38
NC_000014.8:g.54418853T>C , CM000676.1:g.54418853T>C GRCh37
NC_000014.7:g.53488603T>C NCBI36
NG_009215.1:g.9702A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000245451.9:c.88A>G MANE Select ENSP00000245451.4:p.Thr30Ala
ENST00000245451.8:c.88A>G ENSP00000245451.4:p.Thr30Ala
ENST00000417573.5:c.88A>G ENSP00000394165.1:p.Thr30Ala
ENST00000558961.1:c.13A>G ENSP00000453691.1:p.Thr5Ala
ENST00000558984.1:c.88A>G ENSP00000454134.1:p.Thr30Ala
ENST00000559087.5:c.88A>G ENSP00000453485.1:p.Thr30Ala
ENST00000559501.1:c.-102A>G ENSP00000453365.1:n.-102A>G
ENST00000559642.1:c.88A>G ENSP00000453467.1:p.Thr30Ala
NM_001202.3:c.88A>G NP_001193.2:p.Thr30Ala
NM_130850.2:c.88A>G NP_570911.2:p.Thr30Ala
NM_130851.2:c.88A>G NP_570912.2:p.Thr30Ala
XM_005268015.3:c.88A>G XP_005268072.1:p.Thr30Ala
NM_001202.5:c.88A>G NP_001193.2:p.Thr30Ala
NM_001347912.1:c.229A>G NP_001334841.1:p.Thr77Ala
NM_001347913.1:c.-102A>G NP_001334842.1:n.-102A>G
NM_001347914.1:c.88A>G NP_001334843.1:p.Thr30Ala
NM_001347915.1:c.-102A>G NP_001334844.1:n.-102A>G
NM_001347916.1:c.88A>G NP_001334845.1:p.Thr30Ala
NM_001347917.1:c.-102A>G NP_001334846.1:n.-102A>G
NM_130850.4:c.88A>G NP_570911.2:p.Thr30Ala
NM_130851.3:c.88A>G NP_570912.2:p.Thr30Ala
NM_001202.6:c.88A>G MANE Select NP_001193.2:p.Thr30Ala
NM_130850.5:c.88A>G NP_570911.2:p.Thr30Ala
NM_001347913.2:c.-102A>G NP_001334842.1:n.-102A>G
NM_001347914.2:c.88A>G NP_001334843.1:p.Thr30Ala
NM_001347915.2:c.-102A>G NP_001334844.1:n.-102A>G
NM_130851.4:c.88A>G NP_570912.2:p.Thr30Ala