Canonical Allele Identifier: CA2617039190

Gene: ADIPOR2

Linked Data

• gnomAD v4: 12-1787558-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1787558T>C , CM000674.2:g.1787558T>C	GRCh38
NC_000012.11:g.1896724T>C , CM000674.1:g.1896724T>C	GRCh37
NC_000012.10:g.1766985T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.*1486T>C MANE Select	ENSP00000349616.4:n.*1486T>C
ENST00000357103.4:c.*1486T>C	ENSP00000349616.4:n.*1486T>C
NM_024551.2:c.*1486T>C	NP_078827.2:n.*1486T>C
XM_005253789.1:c.*1486T>C	XP_005253846.1:n.*1486T>C
XM_006719018.1:c.*1486T>C	XP_006719081.1:n.*1486T>C
XM_011521024.1:c.*1486T>C	XP_011519326.1:n.*1486T>C
XM_011521025.1:c.*1486T>C	XP_011519327.1:n.*1486T>C
XM_005253789.2:c.*1486T>C	XP_005253846.1:n.*1486T>C
XM_006719018.2:c.*1486T>C	XP_006719081.1:n.*1486T>C
XM_011521024.2:c.*1486T>C	XP_011519326.1:n.*1486T>C
NM_024551.3:c.*1486T>C MANE Select	NP_078827.2:n.*1486T>C
NM_001375363.1:c.*1486T>C	NP_001362292.1:n.*1486T>C
NM_001375364.1:c.*1486T>C	NP_001362293.1:n.*1486T>C
NM_001375365.1:c.*1486T>C	NP_001362294.1:n.*1486T>C