Canonical Allele Identifier: CA1470731327

Gene: BMP2K

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78865673C= , CM000666.2:g.78865673C=	GRCh38
NC_000004.11:g.79786827C= , CM000666.1:g.79786827C=	GRCh37
NC_000004.10:g.80005851C=	NCBI36
NG_047162.1:g.94296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.1184C= MANE Select	ENSP00000424668.2:p.Pro395=
ENST00000335016.9:c.1184C=	ENSP00000334836.5:p.Pro395=
ENST00000389010.7:c.*160C=	ENSP00000373662.3:n.*160C=
ENST00000502613.1:c.261C=
ENST00000502871.5:c.1184C=	ENSP00000421768.1:p.Pro395=
ENST00000505725.1:n.466C=
ENST00000628286.1:c.*160C=	ENSP00000487317.1:n.*160C=
NM_017593.3:c.1184C=	NP_060063.2:p.Pro395=
NM_198892.1:c.1184C=	NP_942595.1:p.Pro395=
XM_005263117.1:c.1184C=	XP_005263174.1:p.Pro395=
XM_011532101.1:c.944C=	XP_011530403.1:p.Pro315=
XM_011532102.1:c.1184C=	XP_011530404.1:p.Pro395=
XM_017008381.1:c.944C=	XP_016863870.1:p.Pro315=
XM_017008382.1:c.296C=	XP_016863871.1:p.Pro99=
NM_017593.4:c.1184C=	NP_060063.2:p.Pro395=
NM_017593.5:c.1184C=	NP_060063.2:p.Pro395=
NM_198892.2:c.1184C= MANE Select	NP_942595.1:p.Pro395=