Canonical Allele Identifier: CA2671525122
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420817-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420817C>T , CM000666.2:g.99420817C>T GRCh38
NC_000004.11:g.100341974C>T , CM000666.1:g.100341974C>T GRCh37
NC_000004.10:g.100560997C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-24G>A MANE Select ENSP00000414254.2:n.565-24G>A
ENST00000209665.8:c.601-24G>A ENSP00000209665.4:n.601-24G>A
ENST00000437033.6:c.565-24G>A ENSP00000414254.2:n.565-24G>A
ENST00000476959.5:c.625-24G>A ENSP00000420269.1:n.625-24G>A
ENST00000482593.5:c.394-24G>A ENSP00000420613.1:n.394-24G>A
NM_000673.4:c.601-24G>A NP_000664.2:n.601-24G>A
NM_001166504.1:c.625-24G>A NP_001159976.1:n.625-24G>A
NM_000673.7:c.565-24G>A MANE Select NP_000664.3:n.565-24G>A
NM_001166504.2:c.625-24G>A NP_001159976.1:n.625-24G>A
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