Canonical Allele Identifier: CA437396601
Gene: ADIPOQ HGNC NCBI

Linked Data

dbSNP Id: rs1272464547
gnomAD v2: 3-186561448-T-TA
gnomAD v3: 3-186843659-T-TA
gnomAD v4: 3-186843659-T-TA
MyVariant Identifiers: chr3:g.186561448_186561449insA (hg19) chr3:g.186561449delinsAC (hg19) chr3:g.186843659_186843660insA (hg38) chr3:g.186843660delinsAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186843659_186843660insA , CM000665.2:g.186843659_186843660insA GRCh38
NC_000003.11:g.186561448_186561449insA , CM000665.1:g.186561448_186561449insA GRCh37
NC_000003.10:g.188044142_188044143insA NCBI36
NG_021140.1:g.5986_5987insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.-9+910_-9+911insA MANE Select ENSP00000320709.2:n.-9+910_-9+911insA
ENST00000320741.6:c.-9+910_-9+911insA ENSP00000320709.2:n.-9+910_-9+911insA
ENST00000444204.2:c.-60+910_-60+911insA ENSP00000389814.2:n.-60+910_-60+911insA
NM_001177800.1:c.-60+910_-60+911insA NP_001171271.1:n.-60+910_-60+911insA
NM_004797.3:c.-9+910_-9+911insA NP_004788.1:n.-9+910_-9+911insA
XM_011513324.1:c.-125+910_-125+911insA XP_011511626.1:n.-125+910_-125+911insA
NM_004797.4:c.-9+910_-9+911insA MANE Select NP_004788.1:n.-9+910_-9+911insA
NM_001177800.2:c.-60+910_-60+911insA NP_001171271.1:n.-60+910_-60+911insA
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