Canonical Allele Identifier: CA1479994146
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420625C= , CM000666.2:g.99420625C= GRCh38
NC_000004.11:g.100341782C= , CM000666.1:g.100341782C= GRCh37
NC_000004.10:g.100560805C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.733G= MANE Select ENSP00000414254.2:p.Asp245=
ENST00000209665.8:c.769G= ENSP00000209665.4:p.Asp257=
ENST00000437033.6:c.733G= ENSP00000414254.2:p.Asp245=
ENST00000476959.5:c.793G= ENSP00000420269.1:p.Asp265=
ENST00000482593.5:c.562G= ENSP00000420613.1:p.Asp188=
NM_000673.4:c.769G= NP_000664.2:p.Asp257=
NM_001166504.1:c.793G= NP_001159976.1:p.Asp265=
NM_000673.7:c.733G= MANE Select NP_000664.3:p.Asp245=
NM_001166504.2:c.793G= NP_001159976.1:p.Asp265=