Canonical Allele Identifier: CA1479994322
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420695C= , CM000666.2:g.99420695C= GRCh38
NC_000004.11:g.100341852C= , CM000666.1:g.100341852C= GRCh37
NC_000004.10:g.100560875C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.663G= MANE Select ENSP00000414254.2:p.Gly221=
ENST00000209665.8:c.699G= ENSP00000209665.4:p.Gly233=
ENST00000437033.6:c.663G= ENSP00000414254.2:p.Gly221=
ENST00000476959.5:c.723G= ENSP00000420269.1:p.Gly241=
ENST00000482593.5:c.492G= ENSP00000420613.1:p.Gly164=
NM_000673.4:c.699G= NP_000664.2:p.Gly233=
NM_001166504.1:c.723G= NP_001159976.1:p.Gly241=
NM_000673.7:c.663G= MANE Select NP_000664.3:p.Gly221=
NM_001166504.2:c.723G= NP_001159976.1:p.Gly241=