Canonical Allele Identifier: CA440506386
Gene: ADH7 HGNC NCBI

Linked Data

gnomAD v4: 4-99420593-T-G
MyVariant Identifiers: chr4:g.100341750T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420593T>G , CM000666.2:g.99420593T>G GRCh38
NC_000004.11:g.100341750T>G , CM000666.1:g.100341750T>G GRCh37
NC_000004.10:g.100560773T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.765A>C MANE Select ENSP00000414254.2:p.Ser255=
ENST00000209665.8:c.801A>C ENSP00000209665.4:p.Ser267=
ENST00000437033.6:c.765A>C ENSP00000414254.2:p.Ser255=
ENST00000476959.5:c.825A>C ENSP00000420269.1:p.Ser275=
ENST00000482593.5:c.594A>C ENSP00000420613.1:p.Ser198=
NM_000673.4:c.801A>C NP_000664.2:p.Ser267=
NM_001166504.1:c.825A>C NP_001159976.1:p.Ser275=
NM_000673.7:c.765A>C MANE Select NP_000664.3:p.Ser255=
NM_001166504.2:c.825A>C NP_001159976.1:p.Ser275=
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