Canonical Allele Identifier: CA1479837977
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99087853A= , CM000666.2:g.99087853A= GRCh38
NC_000004.11:g.100009004A= , CM000666.1:g.100009004A= GRCh37
NC_000004.10:g.100228027A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.12+836T= MANE Select ENSP00000296412.8:n.12+836T=
ENST00000296412.13:c.12+836T= ENSP00000296412.8:n.12+836T=
ENST00000296412.12:c.12+836T= ENSP00000296412.8:n.12+836T=
ENST00000502386.1:c.12+836T= ENSP00000427026.1:n.12+836T=
ENST00000502590.5:c.12+836T= ENSP00000422119.1:n.12+836T=
ENST00000505652.1:c.12+836T= ENSP00000421556.1:n.12+836T=
ENST00000507102.5:n.25+836T=
ENST00000508146.5:n.113+836T=
ENST00000508511.5:n.29+836T=
ENST00000512659.5:c.12+836T= ENSP00000424650.1:n.12+836T=
ENST00000626055.2:c.12+836T= ENSP00000487496.1:n.12+836T=
NM_000671.4:c.12+836T= MANE Select NP_000662.3:n.12+836T=