Canonical Allele Identifier: CA1470756855

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911797C= , CM000666.2:g.78911797C=	GRCh38
NC_000004.11:g.79832951C= , CM000666.1:g.79832951C=	GRCh37
NC_000004.10:g.80051975C=	NCBI36
NG_047162.1:g.140420C=
NG_053104.1:g.32642G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3250C= (BMP2K) MANE Select	ENSP00000424668.2:p.Pro1084=
ENST00000335016.9:c.3250C= (BMP2K)	ENSP00000334836.5:p.Pro1084=
ENST00000342820.10:c.*782+3413G= (PAQR3)	ENSP00000344203.6:n.*782+3413G=
ENST00000502613.1:c.2327C= (BMP2K)
ENST00000511594.5:c.*392G= (PAQR3)	ENSP00000425080.1:n.*392G=
ENST00000512760.5:c.*792+3413G= (PAQR3)	ENSP00000426875.1:n.*792+3413G=
ENST00000628286.1:c.*2226C= (BMP2K)	ENSP00000487317.1:n.*2226C=
NM_198892.1:c.3250C= (BMP2K)	NP_942595.1:p.Pro1084=
XM_005263117.1:c.3139C= (BMP2K)	XP_005263174.1:p.Pro1047=
XM_011532101.1:c.3010C= (BMP2K)	XP_011530403.1:p.Pro1004=
XR_938694.1:n.1118-5636G= (PAQR3)
XM_017008381.1:c.3010C= (BMP2K)	XP_016863870.1:p.Pro1004=
XM_017008382.1:c.2362C= (BMP2K)	XP_016863871.1:p.Pro788=
XR_938694.3:n.1098-5636G= (PAQR3)
NM_198892.2:c.3250C= (BMP2K) MANE Select	NP_942595.1:p.Pro1084=