Canonical Allele Identifier: CA2012138936
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1780590_1780592delinsCCA , CM000674.2:g.1780590_1780592delinsCCA GRCh38
NC_000012.11:g.1889756_1889758delinsCCA , CM000674.1:g.1889756_1889758delinsCCA GRCh37
NC_000012.10:g.1760017_1760019delinsCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.603_605delinsCCA MANE Select ENSP00000349616.4:p.Phe201=
ENST00000357103.4:c.603_605delinsCCA ENSP00000349616.4:p.Phe201=
ENST00000537190.1:n.443_445delinsCCA
NM_024551.2:c.603_605delinsCCA NP_078827.2:p.Phe201=
XM_005253789.1:c.603_605delinsCCA XP_005253846.1:p.Phe201=
XM_006719018.1:c.603_605delinsCCA XP_006719081.1:p.Phe201=
XM_011521024.1:c.603_605delinsCCA XP_011519326.1:p.Phe201=
XM_011521025.1:c.463+2565_463+2567delinsCCA XP_011519327.1:n.463+2565_463+2567delinsCCA
XM_005253789.2:c.603_605delinsCCA XP_005253846.1:p.Phe201=
XM_006719018.2:c.603_605delinsCCA XP_006719081.1:p.Phe201=
XM_011521024.2:c.603_605delinsCCA XP_011519326.1:p.Phe201=
NM_024551.3:c.603_605delinsCCA MANE Select NP_078827.2:p.Phe201=
NM_001375363.1:c.603_605delinsCCA NP_001362292.1:p.Phe201=
NM_001375364.1:c.603_605delinsCCA NP_001362293.1:p.Phe201=
NM_001375365.1:c.603_605delinsCCA NP_001362294.1:p.Phe201=