Canonical Allele Identifier: CA2012138928
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780566C= , CM000674.2:g.1780566C= GRCh38
NC_000012.11:g.1889732C= , CM000674.1:g.1889732C= GRCh37
NC_000012.10:g.1759993C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.579C= MANE Select ENSP00000349616.4:p.Leu193=
ENST00000357103.4:c.579C= ENSP00000349616.4:p.Leu193=
ENST00000537190.1:n.419C=
NM_024551.2:c.579C= NP_078827.2:p.Leu193=
XM_005253789.1:c.579C= XP_005253846.1:p.Leu193=
XM_006719018.1:c.579C= XP_006719081.1:p.Leu193=
XM_011521024.1:c.579C= XP_011519326.1:p.Leu193=
XM_011521025.1:c.463+2541C= XP_011519327.1:n.463+2541C=
XM_005253789.2:c.579C= XP_005253846.1:p.Leu193=
XM_006719018.2:c.579C= XP_006719081.1:p.Leu193=
XM_011521024.2:c.579C= XP_011519326.1:p.Leu193=
NM_024551.3:c.579C= MANE Select NP_078827.2:p.Leu193=
NM_001375363.1:c.579C= NP_001362292.1:p.Leu193=
NM_001375364.1:c.579C= NP_001362293.1:p.Leu193=
NM_001375365.1:c.579C= NP_001362294.1:p.Leu193=