Canonical Allele Identifier: CA1470756674

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911377A= , CM000666.2:g.78911377A=	GRCh38
NC_000004.11:g.79832531A= , CM000666.1:g.79832531A=	GRCh37
NC_000004.10:g.80051555A=	NCBI36
NG_047162.1:g.140000A=
NG_053104.1:g.33062T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2830A= (BMP2K) MANE Select	ENSP00000424668.2:p.Thr944=
ENST00000335016.9:c.2830A= (BMP2K)	ENSP00000334836.5:p.Thr944=
ENST00000342820.10:c.*782+3833T= (PAQR3)	ENSP00000344203.6:n.*782+3833T=
ENST00000502613.1:c.1907A= (BMP2K)
ENST00000511594.5:c.*812T= (PAQR3)	ENSP00000425080.1:n.*812T=
ENST00000512760.5:c.*792+3833T= (PAQR3)	ENSP00000426875.1:n.*792+3833T=
ENST00000628286.1:c.*1806A= (BMP2K)	ENSP00000487317.1:n.*1806A=
NM_198892.1:c.2830A= (BMP2K)	NP_942595.1:p.Thr944=
XM_005263117.1:c.2719A= (BMP2K)	XP_005263174.1:p.Thr907=
XM_011532101.1:c.2590A= (BMP2K)	XP_011530403.1:p.Thr864=
XR_938694.1:n.1118-5216T= (PAQR3)
XM_017008381.1:c.2590A= (BMP2K)	XP_016863870.1:p.Thr864=
XM_017008382.1:c.1942A= (BMP2K)	XP_016863871.1:p.Thr648=
XR_938694.3:n.1098-5216T= (PAQR3)
NM_198892.2:c.2830A= (BMP2K) MANE Select	NP_942595.1:p.Thr944=