Canonical Allele Identifier: CA1470756656

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911342T= , CM000666.2:g.78911342T=	GRCh38
NC_000004.11:g.79832496T= , CM000666.1:g.79832496T=	GRCh37
NC_000004.10:g.80051520T=	NCBI36
NG_047162.1:g.139965T=
NG_053104.1:g.33097A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2795T= (BMP2K) MANE Select	ENSP00000424668.2:p.Phe932=
ENST00000335016.9:c.2795T= (BMP2K)	ENSP00000334836.5:p.Phe932=
ENST00000342820.10:c.*782+3868A= (PAQR3)	ENSP00000344203.6:n.*782+3868A=
ENST00000502613.1:c.1872T= (BMP2K)
ENST00000511594.5:c.*847A= (PAQR3)	ENSP00000425080.1:n.*847A=
ENST00000512760.5:c.*792+3868A= (PAQR3)	ENSP00000426875.1:n.*792+3868A=
ENST00000628286.1:c.*1771T= (BMP2K)	ENSP00000487317.1:n.*1771T=
NM_198892.1:c.2795T= (BMP2K)	NP_942595.1:p.Phe932=
XM_005263117.1:c.2684T= (BMP2K)	XP_005263174.1:p.Phe895=
XM_011532101.1:c.2555T= (BMP2K)	XP_011530403.1:p.Phe852=
XR_938694.1:n.1118-5181A= (PAQR3)
XM_017008381.1:c.2555T= (BMP2K)	XP_016863870.1:p.Phe852=
XM_017008382.1:c.1907T= (BMP2K)	XP_016863871.1:p.Phe636=
XR_938694.3:n.1098-5181A= (PAQR3)
NM_198892.2:c.2795T= (BMP2K) MANE Select	NP_942595.1:p.Phe932=