Canonical Allele Identifier: CA548466371
Gene: ADIPOQ HGNC NCBI

Linked Data

dbSNP Id: rs35615373
gnomAD v2: 3-186561449-CAA-C
gnomAD v3: 3-186843660-CAA-C
gnomAD v4: 3-186843660-CAA-C
MyVariant Identifiers: chr3:g.186561451_186561452del (hg19) chr3:g.186561450_186561451del (hg19) chr3:g.186843662_186843663del (hg38) chr3:g.186843661_186843662del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186843675_186843676del , CM000665.2:g.186843675_186843676del GRCh38
NC_000003.11:g.186561464_186561465del , CM000665.1:g.186561464_186561465del GRCh37
NC_000003.10:g.188044158_188044159del NCBI36
NG_021140.1:g.6002_6003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000320741.7:c.-9+926_-9+927del MANE Select ENSP00000320709.2:n.-9+926_-9+927del
ENST00000320741.6:c.-9+926_-9+927del ENSP00000320709.2:n.-9+926_-9+927del
ENST00000444204.2:c.-60+926_-60+927del ENSP00000389814.2:n.-60+926_-60+927del
NM_001177800.1:c.-60+926_-60+927del NP_001171271.1:n.-60+926_-60+927del
NM_004797.3:c.-9+926_-9+927del NP_004788.1:n.-9+926_-9+927del
XM_011513324.1:c.-125+926_-125+927del XP_011511626.1:n.-125+926_-125+927del
NM_004797.4:c.-9+926_-9+927del MANE Select NP_004788.1:n.-9+926_-9+927del
NM_001177800.2:c.-60+926_-60+927del NP_001171271.1:n.-60+926_-60+927del
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