Canonical Allele Identifier: CA1479994170
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420634T= , CM000666.2:g.99420634T= GRCh38
NC_000004.11:g.100341791T= , CM000666.1:g.100341791T= GRCh37
NC_000004.10:g.100560814T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.724A= MANE Select ENSP00000414254.2:p.Ser242=
ENST00000209665.8:c.760A= ENSP00000209665.4:p.Ser254=
ENST00000437033.6:c.724A= ENSP00000414254.2:p.Ser242=
ENST00000476959.5:c.784A= ENSP00000420269.1:p.Ser262=
ENST00000482593.5:c.553A= ENSP00000420613.1:p.Ser185=
NM_000673.4:c.760A= NP_000664.2:p.Ser254=
NM_001166504.1:c.784A= NP_001159976.1:p.Ser262=
NM_000673.7:c.724A= MANE Select NP_000664.3:p.Ser242=
NM_001166504.2:c.784A= NP_001159976.1:p.Ser262=