Canonical Allele Identifier: CA2137820211
Gene: BMP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53952396A= , CM000676.2:g.53952396A= GRCh38
NC_000014.8:g.54419114A= , CM000676.1:g.54419114A= GRCh37
NC_000014.7:g.53488864A= NCBI36
NG_009215.1:g.9441T=

Transcript Alleles

HGVS Amino-acid change
ENST00000245451.9:c.-7-167T= MANE Select ENSP00000245451.4:n.-7-167T=
ENST00000245451.8:c.-7-167T= ENSP00000245451.4:n.-7-167T=
ENST00000417573.5:c.-7-167T= ENSP00000394165.1:n.-7-167T=
ENST00000558984.1:c.-7-167T= ENSP00000454134.1:n.-7-167T=
ENST00000559087.5:c.-7-167T= ENSP00000453485.1:n.-7-167T=
ENST00000559501.1:c.-143-220T= ENSP00000453365.1:n.-143-220T=
ENST00000559642.1:c.-7-167T= ENSP00000453467.1:n.-7-167T=
NM_001202.3:c.-7-167T= NP_001193.2:n.-7-167T=
NM_130850.2:c.-7-167T= NP_570911.2:n.-7-167T=
NM_130851.2:c.-7-167T= NP_570912.2:n.-7-167T=
XM_005268015.3:c.-7-167T= XP_005268072.1:n.-7-167T=
NM_001202.5:c.-7-167T= NP_001193.2:n.-7-167T=
NM_001347912.1:c.188-220T= NP_001334841.1:n.188-220T=
NM_001347913.1:c.-143-220T= NP_001334842.1:n.-143-220T=
NM_001347914.1:c.-7-167T= NP_001334843.1:n.-7-167T=
NM_001347915.1:c.-143-220T= NP_001334844.1:n.-143-220T=
NM_001347916.1:c.-7-167T= NP_001334845.1:n.-7-167T=
NM_001347917.1:c.-143-220T= NP_001334846.1:n.-143-220T=
NM_130850.4:c.-7-167T= NP_570911.2:n.-7-167T=
NM_130851.3:c.-7-167T= NP_570912.2:n.-7-167T=
NM_001202.6:c.-7-167T= MANE Select NP_001193.2:n.-7-167T=
NM_130850.5:c.-7-167T= NP_570911.2:n.-7-167T=
NM_001347913.2:c.-143-220T= NP_001334842.1:n.-143-220T=
NM_001347914.2:c.-7-167T= NP_001334843.1:n.-7-167T=
NM_001347915.2:c.-143-220T= NP_001334844.1:n.-143-220T=
NM_130851.4:c.-7-167T= NP_570912.2:n.-7-167T=