Canonical Allele Identifier: CA2012110639
Gene: ADIPOR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1719380G= , CM000674.2:g.1719380G= GRCh38
NC_000012.11:g.1828546G= , CM000674.1:g.1828546G= GRCh37
NC_000012.10:g.1698807G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357103.5:c.-87+28189G= MANE Select ENSP00000349616.4:n.-87+28189G=
ENST00000357103.4:c.-87+28189G= ENSP00000349616.4:n.-87+28189G=
ENST00000537545.1:n.144+30663G=
ENST00000540974.1:n.149-11345G=
NM_024551.2:c.-87+28189G= NP_078827.2:n.-87+28189G=
XM_005253789.1:c.-87+28167G= XP_005253846.1:n.-87+28167G=
XM_006719018.1:c.-87+16398G= XP_006719081.1:n.-87+16398G=
XM_011521024.1:c.-87+16398G= XP_011519326.1:n.-87+16398G=
XM_011521025.1:c.-87+28167G= XP_011519327.1:n.-87+28167G=
XM_005253789.2:c.-87+28167G= XP_005253846.1:n.-87+28167G=
XM_006719018.2:c.-87+16398G= XP_006719081.1:n.-87+16398G=
XM_011521024.2:c.-87+16398G= XP_011519326.1:n.-87+16398G=
NM_024551.3:c.-87+28189G= MANE Select NP_078827.2:n.-87+28189G=
NM_001375363.1:c.-87+28189G= NP_001362292.1:n.-87+28189G=
NM_001375364.1:c.-248-16699G= NP_001362293.1:n.-248-16699G=
NM_001375365.1:c.-87+28167G= NP_001362294.1:n.-87+28167G=