Canonical Allele Identifier: CA89669375

Gene: ADIPOQ

Linked Data

• dbSNP Id: rs1024962261
• gnomAD v3: 3-186842900-ACT-A
• gnomAD v4: 3-186842900-ACT-A
• MyVariant Identifiers: chr3:g.186560690_186560691del (hg19) ; chr3:g.186842901_186842902del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186842901_186842902del , CM000665.2:g.186842901_186842902del	GRCh38
NC_000003.11:g.186560690_186560691del , CM000665.1:g.186560690_186560691del	GRCh37
NC_000003.10:g.188043384_188043385del	NCBI36
NG_021140.1:g.5228_5229del

Transcript Alleles

HGVS	Amino-acid change
ENST00000320741.7:c.-9+152_-9+153del MANE Select	ENSP00000320709.2:n.-9+152_-9+153del
ENST00000320741.6:c.-9+152_-9+153del	ENSP00000320709.2:n.-9+152_-9+153del
ENST00000444204.2:c.-60+152_-60+153del	ENSP00000389814.2:n.-60+152_-60+153del
NM_001177800.1:c.-60+152_-60+153del	NP_001171271.1:n.-60+152_-60+153del
NM_004797.3:c.-9+152_-9+153del	NP_004788.1:n.-9+152_-9+153del
XM_011513324.1:c.-125+152_-125+153del	XP_011511626.1:n.-125+152_-125+153del
NM_004797.4:c.-9+152_-9+153del MANE Select	NP_004788.1:n.-9+152_-9+153del
NM_001177800.2:c.-60+152_-60+153del	NP_001171271.1:n.-60+152_-60+153del