Canonical Allele Identifier: CA2137819098

Gene: BMP4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53951918G= , CM000676.2:g.53951918G=	GRCh38
NC_000014.8:g.54418636G= , CM000676.1:g.54418636G=	GRCh37
NC_000014.7:g.53488386G=	NCBI36
NG_009215.1:g.9919C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245451.9:c.305C= MANE Select	ENSP00000245451.4:p.Thr102=
ENST00000245451.8:c.305C=	ENSP00000245451.4:p.Thr102=
ENST00000417573.5:c.305C=	ENSP00000394165.1:p.Thr102=
ENST00000558961.1:c.230C=	ENSP00000453691.1:p.Thr77=
ENST00000558984.1:c.305C=	ENSP00000454134.1:p.Thr102=
ENST00000559087.5:c.305C=	ENSP00000453485.1:p.Thr102=
ENST00000559501.1:c.116C=	ENSP00000453365.1:p.Thr39=
ENST00000559642.1:c.305C=	ENSP00000453467.1:p.Thr102=
NM_001202.3:c.305C=	NP_001193.2:p.Thr102=
NM_130850.2:c.305C=	NP_570911.2:p.Thr102=
NM_130851.2:c.305C=	NP_570912.2:p.Thr102=
XM_005268015.3:c.305C=	XP_005268072.1:p.Thr102=
NM_001202.5:c.305C=	NP_001193.2:p.Thr102=
NM_001347912.1:c.446C=	NP_001334841.1:p.Thr149=
NM_001347913.1:c.116C=	NP_001334842.1:p.Thr39=
NM_001347914.1:c.305C=	NP_001334843.1:p.Thr102=
NM_001347915.1:c.116C=	NP_001334844.1:p.Thr39=
NM_001347916.1:c.305C=	NP_001334845.1:p.Thr102=
NM_001347917.1:c.116C=	NP_001334846.1:p.Thr39=
NM_130850.4:c.305C=	NP_570911.2:p.Thr102=
NM_130851.3:c.305C=	NP_570912.2:p.Thr102=
NM_001202.6:c.305C= MANE Select	NP_001193.2:p.Thr102=
NM_130850.5:c.305C=	NP_570911.2:p.Thr102=
NM_001347913.2:c.116C=	NP_001334842.1:p.Thr39=
NM_001347914.2:c.305C=	NP_001334843.1:p.Thr102=
NM_001347915.2:c.116C=	NP_001334844.1:p.Thr39=
NM_130851.4:c.305C=	NP_570912.2:p.Thr102=