Canonical Allele Identifier: CA1427132845

Gene: ADIPOQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186843652_186843654delinsCTT , CM000665.2:g.186843652_186843654delinsCTT	GRCh38
NC_000003.11:g.186561441_186561443delinsCTT , CM000665.1:g.186561441_186561443delinsCTT	GRCh37
NC_000003.10:g.188044135_188044137delinsCTT	NCBI36
NG_021140.1:g.5979_5981delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320741.7:c.-9+903_-9+905delinsCTT MANE Select	ENSP00000320709.2:n.-9+903_-9+905delinsCTT
ENST00000320741.6:c.-9+903_-9+905delinsCTT	ENSP00000320709.2:n.-9+903_-9+905delinsCTT
ENST00000444204.2:c.-60+903_-60+905delinsCTT	ENSP00000389814.2:n.-60+903_-60+905delinsCTT
NM_001177800.1:c.-60+903_-60+905delinsCTT	NP_001171271.1:n.-60+903_-60+905delinsCTT
NM_004797.3:c.-9+903_-9+905delinsCTT	NP_004788.1:n.-9+903_-9+905delinsCTT
XM_011513324.1:c.-125+903_-125+905delinsCTT	XP_011511626.1:n.-125+903_-125+905delinsCTT
NM_004797.4:c.-9+903_-9+905delinsCTT MANE Select	NP_004788.1:n.-9+903_-9+905delinsCTT
NM_001177800.2:c.-60+903_-60+905delinsCTT	NP_001171271.1:n.-60+903_-60+905delinsCTT