Canonical Allele Identifier: CA1479994433
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420767G= , CM000666.2:g.99420767G= GRCh38
NC_000004.11:g.100341924G= , CM000666.1:g.100341924G= GRCh37
NC_000004.10:g.100560947G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.591C= MANE Select ENSP00000414254.2:p.Val197=
ENST00000209665.8:c.627C= ENSP00000209665.4:p.Val209=
ENST00000437033.6:c.591C= ENSP00000414254.2:p.Val197=
ENST00000476959.5:c.651C= ENSP00000420269.1:p.Val217=
ENST00000482593.5:c.420C= ENSP00000420613.1:p.Val140=
NM_000673.4:c.627C= NP_000664.2:p.Val209=
NM_001166504.1:c.651C= NP_001159976.1:p.Val217=
NM_000673.7:c.591C= MANE Select NP_000664.3:p.Val197=
NM_001166504.2:c.651C= NP_001159976.1:p.Val217=