Canonical Allele Identifier: CA1470731205

Gene: BMP2K

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865608A= , CM000666.2:g.78865608A=	GRCh38
NC_000004.11:g.79786762A= , CM000666.1:g.79786762A=	GRCh37
NC_000004.10:g.80005786A=	NCBI36
NG_047162.1:g.94231A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1119A= MANE Select	ENSP00000424668.2:p.Arg373=
ENST00000335016.9:c.1119A=	ENSP00000334836.5:p.Arg373=
ENST00000389010.7:c.*95A=	ENSP00000373662.3:n.*95A=
ENST00000502613.1:c.196A=
ENST00000502871.5:c.1119A=	ENSP00000421768.1:p.Arg373=
ENST00000505725.1:n.401A=
ENST00000628286.1:c.*95A=	ENSP00000487317.1:n.*95A=
NM_017593.3:c.1119A=	NP_060063.2:p.Arg373=
NM_198892.1:c.1119A=	NP_942595.1:p.Arg373=
XM_005263117.1:c.1119A=	XP_005263174.1:p.Arg373=
XM_011532101.1:c.879A=	XP_011530403.1:p.Arg293=
XM_011532102.1:c.1119A=	XP_011530404.1:p.Arg373=
XM_017008381.1:c.879A=	XP_016863870.1:p.Arg293=
XM_017008382.1:c.231A=	XP_016863871.1:p.Arg77=
NM_017593.4:c.1119A=	NP_060063.2:p.Arg373=
NM_017593.5:c.1119A=	NP_060063.2:p.Arg373=
NM_198892.2:c.1119A= MANE Select	NP_942595.1:p.Arg373=