Canonical Allele Identifier: CA2012138946
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780631T= , CM000674.2:g.1780631T= GRCh38
NC_000012.11:g.1889797T= , CM000674.1:g.1889797T= GRCh37
NC_000012.10:g.1760058T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.644T= MANE Select ENSP00000349616.4:p.Phe215=
ENST00000357103.4:c.644T= ENSP00000349616.4:p.Phe215=
ENST00000537190.1:n.484T=
NM_024551.2:c.644T= NP_078827.2:p.Phe215=
XM_005253789.1:c.644T= XP_005253846.1:p.Phe215=
XM_006719018.1:c.644T= XP_006719081.1:p.Phe215=
XM_011521024.1:c.644T= XP_011519326.1:p.Phe215=
XM_011521025.1:c.463+2606T= XP_011519327.1:n.463+2606T=
XM_005253789.2:c.644T= XP_005253846.1:p.Phe215=
XM_006719018.2:c.644T= XP_006719081.1:p.Phe215=
XM_011521024.2:c.644T= XP_011519326.1:p.Phe215=
NM_024551.3:c.644T= MANE Select NP_078827.2:p.Phe215=
NM_001375363.1:c.644T= NP_001362292.1:p.Phe215=
NM_001375364.1:c.644T= NP_001362293.1:p.Phe215=
NM_001375365.1:c.644T= NP_001362294.1:p.Phe215=