Canonical Allele Identifier: CA486658595

Gene: BMP4

Linked Data

• MyVariant Identifiers: chr14:g.54418589T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53951871T>G , CM000676.2:g.53951871T>G	GRCh38
NC_000014.8:g.54418589T>G , CM000676.1:g.54418589T>G	GRCh37
NC_000014.7:g.53488339T>G	NCBI36
NG_009215.1:g.9966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245451.9:c.352A>C MANE Select	ENSP00000245451.4:p.Arg118=
ENST00000245451.8:c.352A>C	ENSP00000245451.4:p.Arg118=
ENST00000417573.5:c.352A>C	ENSP00000394165.1:p.Arg118=
ENST00000558961.1:c.277A>C	ENSP00000453691.1:p.Arg93=
ENST00000558984.1:c.352A>C	ENSP00000454134.1:p.Arg118=
ENST00000559087.5:c.352A>C	ENSP00000453485.1:p.Arg118=
ENST00000559501.1:c.163A>C	ENSP00000453365.1:p.Arg55=
ENST00000609748.1:c.10A>C	ENSP00000476690.1:p.Arg4=
NM_001202.3:c.352A>C	NP_001193.2:p.Arg118=
NM_130850.2:c.352A>C	NP_570911.2:p.Arg118=
NM_130851.2:c.352A>C	NP_570912.2:p.Arg118=
XM_005268015.3:c.352A>C	XP_005268072.1:p.Arg118=
NM_001202.5:c.352A>C	NP_001193.2:p.Arg118=
NM_001347912.1:c.493A>C	NP_001334841.1:p.Arg165=
NM_001347913.1:c.163A>C	NP_001334842.1:p.Arg55=
NM_001347914.1:c.352A>C	NP_001334843.1:p.Arg118=
NM_001347915.1:c.163A>C	NP_001334844.1:p.Arg55=
NM_001347916.1:c.352A>C	NP_001334845.1:p.Arg118=
NM_001347917.1:c.163A>C	NP_001334846.1:p.Arg55=
NM_130850.4:c.352A>C	NP_570911.2:p.Arg118=
NM_130851.3:c.352A>C	NP_570912.2:p.Arg118=
NM_001202.6:c.352A>C MANE Select	NP_001193.2:p.Arg118=
NM_130850.5:c.352A>C	NP_570911.2:p.Arg118=
NM_001347913.2:c.163A>C	NP_001334842.1:p.Arg55=
NM_001347914.2:c.352A>C	NP_001334843.1:p.Arg118=
NM_001347915.2:c.163A>C	NP_001334844.1:p.Arg55=
NM_130851.4:c.352A>C	NP_570912.2:p.Arg118=