Canonical Allele Identifier: CA2012138906

Gene: ADIPOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780495C= , CM000674.2:g.1780495C=	GRCh38
NC_000012.11:g.1889661C= , CM000674.1:g.1889661C=	GRCh37
NC_000012.10:g.1759922C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.508C= MANE Select	ENSP00000349616.4:p.Pro170=
ENST00000357103.4:c.508C=	ENSP00000349616.4:p.Pro170=
ENST00000535774.1:n.465C=
ENST00000537190.1:n.348C=
NM_024551.2:c.508C=	NP_078827.2:p.Pro170=
XM_005253789.1:c.508C=	XP_005253846.1:p.Pro170=
XM_006719018.1:c.508C=	XP_006719081.1:p.Pro170=
XM_011521024.1:c.508C=	XP_011519326.1:p.Pro170=
XM_011521025.1:c.463+2470C=	XP_011519327.1:n.463+2470C=
XM_005253789.2:c.508C=	XP_005253846.1:p.Pro170=
XM_006719018.2:c.508C=	XP_006719081.1:p.Pro170=
XM_011521024.2:c.508C=	XP_011519326.1:p.Pro170=
NM_024551.3:c.508C= MANE Select	NP_078827.2:p.Pro170=
NM_001375363.1:c.508C=	NP_001362292.1:p.Pro170=
NM_001375364.1:c.508C=	NP_001362293.1:p.Pro170=
NM_001375365.1:c.508C=	NP_001362294.1:p.Pro170=