Canonical Allele Identifier: CA2012144958
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1787612C= , CM000674.2:g.1787612C= GRCh38
NC_000012.11:g.1896778C= , CM000674.1:g.1896778C= GRCh37
NC_000012.10:g.1767039C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.*1540C= MANE Select ENSP00000349616.4:n.*1540C=
ENST00000357103.4:c.*1540C= ENSP00000349616.4:n.*1540C=
NM_024551.2:c.*1540C= NP_078827.2:n.*1540C=
XM_005253789.1:c.*1540C= XP_005253846.1:n.*1540C=
XM_006719018.1:c.*1540C= XP_006719081.1:n.*1540C=
XM_011521024.1:c.*1540C= XP_011519326.1:n.*1540C=
XM_011521025.1:c.*1540C= XP_011519327.1:n.*1540C=
XM_005253789.2:c.*1540C= XP_005253846.1:n.*1540C=
XM_006719018.2:c.*1540C= XP_006719081.1:n.*1540C=
XM_011521024.2:c.*1540C= XP_011519326.1:n.*1540C=
NM_024551.3:c.*1540C= MANE Select NP_078827.2:n.*1540C=
NM_001375363.1:c.*1540C= NP_001362292.1:n.*1540C=
NM_001375364.1:c.*1540C= NP_001362293.1:n.*1540C=
NM_001375365.1:c.*1540C= NP_001362294.1:n.*1540C=