Canonical Allele Identifier: CA1480005270
Gene: ADH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99428513C= , CM000666.2:g.99428513C= GRCh38
NC_000004.11:g.100349670C= , CM000666.1:g.100349670C= GRCh37
NC_000004.10:g.100568693C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.238G= MANE Select ENSP00000414254.2:p.Gly80=
ENST00000209665.8:c.274G= ENSP00000209665.4:p.Gly92=
ENST00000437033.6:c.238G= ENSP00000414254.2:p.Gly80=
ENST00000474027.1:c.67G= ENSP00000420300.1:p.Gly23=
ENST00000476959.5:c.298G= ENSP00000420269.1:p.Gly100=
ENST00000482593.5:c.67G= ENSP00000420613.1:p.Gly23=
NM_000673.4:c.274G= NP_000664.2:p.Gly92=
NM_001166504.1:c.298G= NP_001159976.1:p.Gly100=
NM_000673.7:c.238G= MANE Select NP_000664.3:p.Gly80=
NM_001166504.2:c.298G= NP_001159976.1:p.Gly100=