Canonical Allele Identifier: CA2012138901

Gene: ADIPOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780492C= , CM000674.2:g.1780492C=	GRCh38
NC_000012.11:g.1889658C= , CM000674.1:g.1889658C=	GRCh37
NC_000012.10:g.1759919C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.505C= MANE Select	ENSP00000349616.4:p.Arg169=
ENST00000357103.4:c.505C=	ENSP00000349616.4:p.Arg169=
ENST00000535774.1:n.462C=
ENST00000537190.1:n.345C=
NM_024551.2:c.505C=	NP_078827.2:p.Arg169=
XM_005253789.1:c.505C=	XP_005253846.1:p.Arg169=
XM_006719018.1:c.505C=	XP_006719081.1:p.Arg169=
XM_011521024.1:c.505C=	XP_011519326.1:p.Arg169=
XM_011521025.1:c.463+2467C=	XP_011519327.1:n.463+2467C=
XM_005253789.2:c.505C=	XP_005253846.1:p.Arg169=
XM_006719018.2:c.505C=	XP_006719081.1:p.Arg169=
XM_011521024.2:c.505C=	XP_011519326.1:p.Arg169=
NM_024551.3:c.505C= MANE Select	NP_078827.2:p.Arg169=
NM_001375363.1:c.505C=	NP_001362292.1:p.Arg169=
NM_001375364.1:c.505C=	NP_001362293.1:p.Arg169=
NM_001375365.1:c.505C=	NP_001362294.1:p.Arg169=