Canonical Allele Identifier: CA2012137537

Gene: ADIPOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1756729T= , CM000674.2:g.1756729T=	GRCh38
NC_000012.11:g.1865895T= , CM000674.1:g.1865895T=	GRCh37
NC_000012.10:g.1736156T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357103.5:c.171+2215T= MANE Select	ENSP00000349616.4:n.171+2215T=
ENST00000357103.4:c.171+2215T=	ENSP00000349616.4:n.171+2215T=
ENST00000537545.1:n.401+2215T=
NM_024551.2:c.171+2215T=	NP_078827.2:n.171+2215T=
XM_005253789.1:c.171+2215T=	XP_005253846.1:n.171+2215T=
XM_006719018.1:c.171+2215T=	XP_006719081.1:n.171+2215T=
XM_011521024.1:c.171+2215T=	XP_011519326.1:n.171+2215T=
XM_011521025.1:c.171+2215T=	XP_011519327.1:n.171+2215T=
XM_005253789.2:c.171+2215T=	XP_005253846.1:n.171+2215T=
XM_006719018.2:c.171+2215T=	XP_006719081.1:n.171+2215T=
XM_011521024.2:c.171+2215T=	XP_011519326.1:n.171+2215T=
NM_024551.3:c.171+2215T= MANE Select	NP_078827.2:n.171+2215T=
NM_001375363.1:c.171+2215T=	NP_001362292.1:n.171+2215T=
NM_001375364.1:c.171+2215T=	NP_001362293.1:n.171+2215T=
NM_001375365.1:c.171+2215T=	NP_001362294.1:n.171+2215T=