Canonical Allele Identifier: CA2137819592
Gene: BMP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53952206C= , CM000676.2:g.53952206C= GRCh38
NC_000014.8:g.54418924C= , CM000676.1:g.54418924C= GRCh37
NC_000014.7:g.53488674C= NCBI36
NG_009215.1:g.9631G=

Transcript Alleles

HGVS Amino-acid change
ENST00000245451.9:c.17G= MANE Select ENSP00000245451.4:p.Arg6=
ENST00000245451.8:c.17G= ENSP00000245451.4:p.Arg6=
ENST00000417573.5:c.17G= ENSP00000394165.1:p.Arg6=
ENST00000558984.1:c.17G= ENSP00000454134.1:p.Arg6=
ENST00000559087.5:c.17G= ENSP00000453485.1:p.Arg6=
ENST00000559501.1:c.-143-30G= ENSP00000453365.1:n.-143-30G=
ENST00000559642.1:c.17G= ENSP00000453467.1:p.Arg6=
NM_001202.3:c.17G= NP_001193.2:p.Arg6=
NM_130850.2:c.17G= NP_570911.2:p.Arg6=
NM_130851.2:c.17G= NP_570912.2:p.Arg6=
XM_005268015.3:c.17G= XP_005268072.1:p.Arg6=
NM_001202.5:c.17G= NP_001193.2:p.Arg6=
NM_001347912.1:c.188-30G= NP_001334841.1:n.188-30G=
NM_001347913.1:c.-143-30G= NP_001334842.1:n.-143-30G=
NM_001347914.1:c.17G= NP_001334843.1:p.Arg6=
NM_001347915.1:c.-143-30G= NP_001334844.1:n.-143-30G=
NM_001347916.1:c.17G= NP_001334845.1:p.Arg6=
NM_001347917.1:c.-143-30G= NP_001334846.1:n.-143-30G=
NM_130850.4:c.17G= NP_570911.2:p.Arg6=
NM_130851.3:c.17G= NP_570912.2:p.Arg6=
NM_001202.6:c.17G= MANE Select NP_001193.2:p.Arg6=
NM_130850.5:c.17G= NP_570911.2:p.Arg6=
NM_001347913.2:c.-143-30G= NP_001334842.1:n.-143-30G=
NM_001347914.2:c.17G= NP_001334843.1:p.Arg6=
NM_001347915.2:c.-143-30G= NP_001334844.1:n.-143-30G=
NM_130851.4:c.17G= NP_570912.2:p.Arg6=