Canonical Allele Identifier: CA2012144975

Gene: ADIPOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1787641_1787642delinsTG , CM000674.2:g.1787641_1787642delinsTG	GRCh38
NC_000012.11:g.1896807_1896808delinsTG , CM000674.1:g.1896807_1896808delinsTG	GRCh37
NC_000012.10:g.1767068_1767069delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.*1569_*1570delinsTG MANE Select	ENSP00000349616.4:n.*1569_*1570delinsTG
ENST00000357103.4:c.*1569_*1570delinsTG	ENSP00000349616.4:n.*1569_*1570delinsTG
NM_024551.2:c.*1569_*1570delinsTG	NP_078827.2:n.*1569_*1570delinsTG
XM_005253789.1:c.*1569_*1570delinsTG	XP_005253846.1:n.*1569_*1570delinsTG
XM_006719018.1:c.*1569_*1570delinsTG	XP_006719081.1:n.*1569_*1570delinsTG
XM_011521024.1:c.*1569_*1570delinsTG	XP_011519326.1:n.*1569_*1570delinsTG
XM_011521025.1:c.*1569_*1570delinsTG	XP_011519327.1:n.*1569_*1570delinsTG
XM_005253789.2:c.*1569_*1570delinsTG	XP_005253846.1:n.*1569_*1570delinsTG
XM_006719018.2:c.*1569_*1570delinsTG	XP_006719081.1:n.*1569_*1570delinsTG
XM_011521024.2:c.*1569_*1570delinsTG	XP_011519326.1:n.*1569_*1570delinsTG
NM_024551.3:c.*1569_*1570delinsTG MANE Select	NP_078827.2:n.*1569_*1570delinsTG
NM_001375363.1:c.*1569_*1570delinsTG	NP_001362292.1:n.*1569_*1570delinsTG
NM_001375364.1:c.*1569_*1570delinsTG	NP_001362293.1:n.*1569_*1570delinsTG
NM_001375365.1:c.*1569_*1570delinsTG	NP_001362294.1:n.*1569_*1570delinsTG