Canonical Allele Identifier: CA1470756701

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911445G= , CM000666.2:g.78911445G=	GRCh38
NC_000004.11:g.79832599G= , CM000666.1:g.79832599G=	GRCh37
NC_000004.10:g.80051623G=	NCBI36
NG_047162.1:g.140068G=
NG_053104.1:g.32994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.2898G= (BMP2K) MANE Select	ENSP00000424668.2:p.Gln966=
ENST00000335016.9:c.2898G= (BMP2K)	ENSP00000334836.5:p.Gln966=
ENST00000342820.10:c.*782+3765C= (PAQR3)	ENSP00000344203.6:n.*782+3765C=
ENST00000502613.1:c.1975G= (BMP2K)
ENST00000511594.5:c.*744C= (PAQR3)	ENSP00000425080.1:n.*744C=
ENST00000512760.5:c.*792+3765C= (PAQR3)	ENSP00000426875.1:n.*792+3765C=
ENST00000628286.1:c.*1874G= (BMP2K)	ENSP00000487317.1:n.*1874G=
NM_198892.1:c.2898G= (BMP2K)	NP_942595.1:p.Gln966=
XM_005263117.1:c.2787G= (BMP2K)	XP_005263174.1:p.Gln929=
XM_011532101.1:c.2658G= (BMP2K)	XP_011530403.1:p.Gln886=
XR_938694.1:n.1118-5284C= (PAQR3)
XM_017008381.1:c.2658G= (BMP2K)	XP_016863870.1:p.Gln886=
XM_017008382.1:c.2010G= (BMP2K)	XP_016863871.1:p.Gln670=
XR_938694.3:n.1098-5284C= (PAQR3)
NM_198892.2:c.2898G= (BMP2K) MANE Select	NP_942595.1:p.Gln966=