Canonical Allele Identifier: CA2137804338

Gene: BMP4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53956335A= , CM000676.2:g.53956335A=	GRCh38
NC_000014.8:g.54423053A= , CM000676.1:g.54423053A=	GRCh37
NC_000014.7:g.53492803A=	NCBI36
NG_009215.1:g.5502T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001202.6:c.-133+215T= MANE Select	NP_001193.2:n.-133+215T=
ENST00000245451.9:c.-133+215T= MANE Select	ENSP00000245451.4:n.-133+215T=
NM_001202.3:c.-133+215T=	NP_001193.2:n.-133+215T=
NM_001202.5:c.-133+215T=	NP_001193.2:n.-133+215T=
NM_001347912.1:c.62+424T=	NP_001334841.1:n.62+424T=
NM_001347913.1:c.-269+215T=	NP_001334842.1:n.-269+215T=
NM_001347913.2:c.-269+215T=	NP_001334842.1:n.-269+215T=
NM_130850.2:c.-133+424T=	NP_570911.2:n.-133+424T=
NM_130850.4:c.-133+424T=	NP_570911.2:n.-133+424T=
NM_130850.5:c.-133+424T=	NP_570911.2:n.-133+424T=
ENST00000245451.8:c.-133+215T=	ENSP00000245451.4:n.-133+215T=
ENST00000558489.1:n.99+215T=
ENST00000559087.5:c.-133+424T=	ENSP00000453485.1:n.-133+424T=
ENST00000559642.1:c.-133+2385T=	ENSP00000453467.1:n.-133+2385T=