Canonical Allele Identifier: CA1470756877

Gene: BMP2K PAQR3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78911839G= , CM000666.2:g.78911839G=	GRCh38
NC_000004.11:g.79832993G= , CM000666.1:g.79832993G=	GRCh37
NC_000004.10:g.80052017G=	NCBI36
NG_047162.1:g.140462G=
NG_053104.1:g.32600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502613.3:c.3292G= (BMP2K) MANE Select	ENSP00000424668.2:p.Val1098=
ENST00000335016.9:c.3292G= (BMP2K)	ENSP00000334836.5:p.Val1098=
ENST00000342820.10:c.*782+3371C= (PAQR3)	ENSP00000344203.6:n.*782+3371C=
ENST00000502613.1:c.2369G= (BMP2K)
ENST00000511594.5:c.*350C= (PAQR3)	ENSP00000425080.1:n.*350C=
ENST00000512760.5:c.*792+3371C= (PAQR3)	ENSP00000426875.1:n.*792+3371C=
ENST00000628286.1:c.*2268G= (BMP2K)	ENSP00000487317.1:n.*2268G=
NM_198892.1:c.3292G= (BMP2K)	NP_942595.1:p.Val1098=
XM_005263117.1:c.3181G= (BMP2K)	XP_005263174.1:p.Val1061=
XM_011532101.1:c.3052G= (BMP2K)	XP_011530403.1:p.Val1018=
XR_938694.1:n.1118-5678C= (PAQR3)
XM_017008381.1:c.3052G= (BMP2K)	XP_016863870.1:p.Val1018=
XM_017008382.1:c.2404G= (BMP2K)	XP_016863871.1:p.Val802=
XR_938694.3:n.1098-5678C= (PAQR3)
NM_198892.2:c.3292G= (BMP2K) MANE Select	NP_942595.1:p.Val1098=