Canonical Allele Identifier: CA440506435
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420668-C-T
MyVariant Identifiers: chr4:g.100341825C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420668C>T , CM000666.2:g.99420668C>T GRCh38
NC_000004.11:g.100341825C>T , CM000666.1:g.100341825C>T GRCh37
NC_000004.10:g.100560848C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.690G>A MANE Select ENSP00000414254.2:p.Glu230=
ENST00000209665.8:c.726G>A ENSP00000209665.4:p.Glu242=
ENST00000437033.6:c.690G>A ENSP00000414254.2:p.Glu230=
ENST00000476959.5:c.750G>A ENSP00000420269.1:p.Glu250=
ENST00000482593.5:c.519G>A ENSP00000420613.1:p.Glu173=
NM_000673.4:c.726G>A NP_000664.2:p.Glu242=
NM_001166504.1:c.750G>A NP_001159976.1:p.Glu250=
NM_000673.7:c.690G>A MANE Select NP_000664.3:p.Glu230=
NM_001166504.2:c.750G>A NP_001159976.1:p.Glu250=
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