Canonical Allele Identifier: CA2137817830

Gene: BMP4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53950804A= , CM000676.2:g.53950804A=	GRCh38
NC_000014.8:g.54417522A= , CM000676.1:g.54417522A=	GRCh37
NC_000014.7:g.53487272A=	NCBI36
NG_009215.1:g.11033T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000245451.9:c.455T= MANE Select	ENSP00000245451.4:p.Val152=
ENST00000245451.8:c.455T=	ENSP00000245451.4:p.Val152=
ENST00000417573.5:c.455T=	ENSP00000394165.1:p.Val152=
ENST00000558961.1:c.313T=	ENSP00000453691.1:p.Ter105=
ENST00000558984.1:c.455T=	ENSP00000454134.1:p.Val152=
ENST00000559087.5:c.455T=	ENSP00000453485.1:p.Val152=
ENST00000559501.1:c.266T=	ENSP00000453365.1:p.Val89=
NM_001202.3:c.455T=	NP_001193.2:p.Val152=
NM_130850.2:c.455T=	NP_570911.2:p.Val152=
NM_130851.2:c.455T=	NP_570912.2:p.Val152=
XM_005268015.3:c.455T=	XP_005268072.1:p.Val152=
NM_001202.5:c.455T=	NP_001193.2:p.Val152=
NM_001347912.1:c.596T=	NP_001334841.1:p.Val199=
NM_001347913.1:c.266T=	NP_001334842.1:p.Val89=
NM_001347914.1:c.455T=	NP_001334843.1:p.Val152=
NM_001347915.1:c.266T=	NP_001334844.1:p.Val89=
NM_001347916.1:c.455T=	NP_001334845.1:p.Val152=
NM_001347917.1:c.266T=	NP_001334846.1:p.Val89=
NM_130850.4:c.455T=	NP_570911.2:p.Val152=
NM_130851.3:c.455T=	NP_570912.2:p.Val152=
NM_001202.6:c.455T= MANE Select	NP_001193.2:p.Val152=
NM_130850.5:c.455T=	NP_570911.2:p.Val152=
NM_001347913.2:c.266T=	NP_001334842.1:p.Val89=
NM_001347914.2:c.455T=	NP_001334843.1:p.Val152=
NM_001347915.2:c.266T=	NP_001334844.1:p.Val89=
NM_130851.4:c.455T=	NP_570912.2:p.Val152=