Canonical Allele Identifier: CA486658351

Gene: BMP4

Linked Data

• MyVariant Identifiers: chr14:g.54417386T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53950668T>G , CM000676.2:g.53950668T>G	GRCh38
NC_000014.8:g.54417386T>G , CM000676.1:g.54417386T>G	GRCh37
NC_000014.7:g.53487136T>G	NCBI36
NG_009215.1:g.11169A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245451.9:c.591A>C MANE Select	ENSP00000245451.4:p.Thr197=
ENST00000245451.8:c.591A>C	ENSP00000245451.4:p.Thr197=
ENST00000417573.5:c.591A>C	ENSP00000394165.1:p.Thr197=
ENST00000558961.1:c.449A>C	ENSP00000453691.1:n.449A>C
ENST00000558984.1:c.591A>C	ENSP00000454134.1:p.Thr197=
ENST00000559087.5:c.591A>C	ENSP00000453485.1:p.Thr197=
ENST00000559501.1:c.402A>C	ENSP00000453365.1:p.Thr134=
NM_001202.3:c.591A>C	NP_001193.2:p.Thr197=
NM_130850.2:c.591A>C	NP_570911.2:p.Thr197=
NM_130851.2:c.591A>C	NP_570912.2:p.Thr197=
XM_005268015.3:c.591A>C	XP_005268072.1:p.Thr197=
NM_001202.5:c.591A>C	NP_001193.2:p.Thr197=
NM_001347912.1:c.732A>C	NP_001334841.1:p.Thr244=
NM_001347913.1:c.402A>C	NP_001334842.1:p.Thr134=
NM_001347914.1:c.591A>C	NP_001334843.1:p.Thr197=
NM_001347915.1:c.402A>C	NP_001334844.1:p.Thr134=
NM_001347916.1:c.591A>C	NP_001334845.1:p.Thr197=
NM_001347917.1:c.402A>C	NP_001334846.1:p.Thr134=
NM_130850.4:c.591A>C	NP_570911.2:p.Thr197=
NM_130851.3:c.591A>C	NP_570912.2:p.Thr197=
NM_001202.6:c.591A>C MANE Select	NP_001193.2:p.Thr197=
NM_130850.5:c.591A>C	NP_570911.2:p.Thr197=
NM_001347913.2:c.402A>C	NP_001334842.1:p.Thr134=
NM_001347914.2:c.591A>C	NP_001334843.1:p.Thr197=
NM_001347915.2:c.402A>C	NP_001334844.1:p.Thr134=
NM_130851.4:c.591A>C	NP_570912.2:p.Thr197=