Canonical Allele Identifier: CA1479840660
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99077851C= , CM000666.2:g.99077851C= GRCh38
NC_000004.11:g.99999002C= , CM000666.1:g.99999002C= GRCh37
NC_000004.10:g.100218025C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.345-928G= MANE Select ENSP00000296412.8:n.345-928G=
ENST00000296412.13:c.345-928G= ENSP00000296412.8:n.345-928G=
ENST00000296412.12:c.345-928G= ENSP00000296412.8:n.345-928G=
ENST00000502590.5:c.*25-928G= ENSP00000422119.1:n.*25-928G=
ENST00000503130.5:c.306-928G= ENSP00000427049.1:n.306-928G=
ENST00000505652.1:c.*169-928G= ENSP00000421556.1:n.*169-928G=
ENST00000508511.5:n.362-928G=
ENST00000512604.1:n.205-928G=
ENST00000512621.5:n.333-928G=
ENST00000512659.5:c.*32-928G= ENSP00000424650.1:n.*32-928G=
ENST00000512991.5:n.543-928G=
ENST00000626055.2:c.*32-928G= ENSP00000487496.1:n.*32-928G=
NM_000671.4:c.345-928G= MANE Select NP_000662.3:n.345-928G=