Canonical Allele Identifier: CA2762806159
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420877_99420878insCACACCCAAC , CM000666.2:g.99420877_99420878insCACACCCAAC GRCh38
NC_000004.11:g.100342034_100342035insCACACCCAAC , CM000666.1:g.100342034_100342035insCACACCCAAC GRCh37
NC_000004.10:g.100561057_100561058insCACACCCAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-85_565-84insGTTGGGTGTG MANE Select ENSP00000414254.2:n.565-85_565-84insGTTGGGTGTG
ENST00000209665.8:c.601-85_601-84insGTTGGGTGTG ENSP00000209665.4:n.601-85_601-84insGTTGGGTGTG
ENST00000437033.6:c.565-85_565-84insGTTGGGTGTG ENSP00000414254.2:n.565-85_565-84insGTTGGGTGTG
ENST00000476959.5:c.625-85_625-84insGTTGGGTGTG ENSP00000420269.1:n.625-85_625-84insGTTGGGTGTG
ENST00000482593.5:c.394-85_394-84insGTTGGGTGTG ENSP00000420613.1:n.394-85_394-84insGTTGGGTGTG
NM_000673.4:c.601-85_601-84insGTTGGGTGTG NP_000664.2:n.601-85_601-84insGTTGGGTGTG
NM_001166504.1:c.625-85_625-84insGTTGGGTGTG NP_001159976.1:n.625-85_625-84insGTTGGGTGTG
NM_000673.7:c.565-85_565-84insGTTGGGTGTG MANE Select NP_000664.3:n.565-85_565-84insGTTGGGTGTG
NM_001166504.2:c.625-85_625-84insGTTGGGTGTG NP_001159976.1:n.625-85_625-84insGTTGGGTGTG