Canonical Allele Identifier: CA231905996

Gene: ADIPOR2

Linked Data

• dbSNP Id: rs774208001
• MyVariant Identifiers: chr12:g.1896763_1896764insA (hg19) ; chr12:g.1787597_1787598insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.1787598dup , CM000674.2:g.1787598dup	GRCh38
NC_000012.11:g.1896764dup , CM000674.1:g.1896764dup	GRCh37
NC_000012.10:g.1767025dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357103.5:c.*1526dup MANE Select	ENSP00000349616.4:n.*1526dup
ENST00000357103.4:c.*1526dup	ENSP00000349616.4:n.*1526dup
NM_024551.2:c.*1526dup	NP_078827.2:n.*1526dup
XM_005253789.1:c.*1526dup	XP_005253846.1:n.*1526dup
XM_006719018.1:c.*1526dup	XP_006719081.1:n.*1526dup
XM_011521024.1:c.*1526dup	XP_011519326.1:n.*1526dup
XM_011521025.1:c.*1526dup	XP_011519327.1:n.*1526dup
XM_005253789.2:c.*1526dup	XP_005253846.1:n.*1526dup
XM_006719018.2:c.*1526dup	XP_006719081.1:n.*1526dup
XM_011521024.2:c.*1526dup	XP_011519326.1:n.*1526dup
NM_024551.3:c.*1526dup MANE Select	NP_078827.2:n.*1526dup
NM_001375363.1:c.*1526dup	NP_001362292.1:n.*1526dup
NM_001375364.1:c.*1526dup	NP_001362293.1:n.*1526dup
NM_001375365.1:c.*1526dup	NP_001362294.1:n.*1526dup