Canonical Allele Identifier: CA383652067

Gene: ADIPOR2

Linked Data

• COSMIC: COSM692949
• MyVariant Identifiers: chr12:g.1889659G>T (hg19) ; chr12:g.1780493G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1780493G>T , CM000674.2:g.1780493G>T	GRCh38
NC_000012.11:g.1889659G>T , CM000674.1:g.1889659G>T	GRCh37
NC_000012.10:g.1759920G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.506G>T MANE Select	ENSP00000349616.4:p.Arg169Leu
ENST00000357103.4:c.506G>T	ENSP00000349616.4:p.Arg169Leu
ENST00000535774.1:n.463G>T
ENST00000537190.1:n.346G>T
NM_024551.2:c.506G>T	NP_078827.2:p.Arg169Leu
XM_005253789.1:c.506G>T	XP_005253846.1:p.Arg169Leu
XM_006719018.1:c.506G>T	XP_006719081.1:p.Arg169Leu
XM_011521024.1:c.506G>T	XP_011519326.1:p.Arg169Leu
XM_011521025.1:c.463+2468G>T	XP_011519327.1:n.463+2468G>T
XM_005253789.2:c.506G>T	XP_005253846.1:p.Arg169Leu
XM_006719018.2:c.506G>T	XP_006719081.1:p.Arg169Leu
XM_011521024.2:c.506G>T	XP_011519326.1:p.Arg169Leu
NM_024551.3:c.506G>T MANE Select	NP_078827.2:p.Arg169Leu
NM_001375363.1:c.506G>T	NP_001362292.1:p.Arg169Leu
NM_001375364.1:c.506G>T	NP_001362293.1:p.Arg169Leu
NM_001375365.1:c.506G>T	NP_001362294.1:p.Arg169Leu