Canonical Allele Identifier: CA2137819584
Gene: BMP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53952202C= , CM000676.2:g.53952202C= GRCh38
NC_000014.8:g.54418920C= , CM000676.1:g.54418920C= GRCh37
NC_000014.7:g.53488670C= NCBI36
NG_009215.1:g.9635G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000245451.9:c.21G= MANE Select ENSP00000245451.4:p.Met7=
ENST00000245451.8:c.21G= ENSP00000245451.4:p.Met7=
ENST00000417573.5:c.21G= ENSP00000394165.1:p.Met7=
ENST00000558984.1:c.21G= ENSP00000454134.1:p.Met7=
ENST00000559087.5:c.21G= ENSP00000453485.1:p.Met7=
ENST00000559501.1:c.-143-26G= ENSP00000453365.1:n.-143-26G=
ENST00000559642.1:c.21G= ENSP00000453467.1:p.Met7=
NM_001202.3:c.21G= NP_001193.2:p.Met7=
NM_130850.2:c.21G= NP_570911.2:p.Met7=
NM_130851.2:c.21G= NP_570912.2:p.Met7=
XM_005268015.3:c.21G= XP_005268072.1:p.Met7=
NM_001202.5:c.21G= NP_001193.2:p.Met7=
NM_001347912.1:c.188-26G= NP_001334841.1:n.188-26G=
NM_001347913.1:c.-143-26G= NP_001334842.1:n.-143-26G=
NM_001347914.1:c.21G= NP_001334843.1:p.Met7=
NM_001347915.1:c.-143-26G= NP_001334844.1:n.-143-26G=
NM_001347916.1:c.21G= NP_001334845.1:p.Met7=
NM_001347917.1:c.-143-26G= NP_001334846.1:n.-143-26G=
NM_130850.4:c.21G= NP_570911.2:p.Met7=
NM_130851.3:c.21G= NP_570912.2:p.Met7=
NM_001202.6:c.21G= MANE Select NP_001193.2:p.Met7=
NM_130850.5:c.21G= NP_570911.2:p.Met7=
NM_001347913.2:c.-143-26G= NP_001334842.1:n.-143-26G=
NM_001347914.2:c.21G= NP_001334843.1:p.Met7=
NM_001347915.2:c.-143-26G= NP_001334844.1:n.-143-26G=
NM_130851.4:c.21G= NP_570912.2:p.Met7=