Canonical Allele Identifier: CA1065916065
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v3: 4-99421019-A-AG
gnomAD v4: 4-99421019-A-AG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99421019_99421020insG , CM000666.2:g.99421019_99421020insG GRCh38
NC_000004.11:g.100342176_100342177insG , CM000666.1:g.100342176_100342177insG GRCh37
NC_000004.10:g.100561199_100561200insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.565-227_565-226insC MANE Select ENSP00000414254.2:n.565-227_565-226insC
ENST00000209665.8:c.601-227_601-226insC ENSP00000209665.4:n.601-227_601-226insC
ENST00000437033.6:c.565-227_565-226insC ENSP00000414254.2:n.565-227_565-226insC
ENST00000476959.5:c.625-227_625-226insC ENSP00000420269.1:n.625-227_625-226insC
ENST00000482593.5:c.394-227_394-226insC ENSP00000420613.1:n.394-227_394-226insC
NM_000673.4:c.601-227_601-226insC NP_000664.2:n.601-227_601-226insC
NM_001166504.1:c.625-227_625-226insC NP_001159976.1:n.625-227_625-226insC
NM_000673.7:c.565-227_565-226insC MANE Select NP_000664.3:n.565-227_565-226insC
NM_001166504.2:c.625-227_625-226insC NP_001159976.1:n.625-227_625-226insC
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