Canonical Allele Identifier: CA1479840606
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99077795A= , CM000666.2:g.99077795A= GRCh38
NC_000004.11:g.99998946A= , CM000666.1:g.99998946A= GRCh37
NC_000004.10:g.100217969A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.345-872T= MANE Select ENSP00000296412.8:n.345-872T=
ENST00000296412.13:c.345-872T= ENSP00000296412.8:n.345-872T=
ENST00000296412.12:c.345-872T= ENSP00000296412.8:n.345-872T=
ENST00000502590.5:c.*25-872T= ENSP00000422119.1:n.*25-872T=
ENST00000503130.5:c.306-872T= ENSP00000427049.1:n.306-872T=
ENST00000505652.1:c.*169-872T= ENSP00000421556.1:n.*169-872T=
ENST00000508511.5:n.362-872T=
ENST00000512604.1:n.205-872T=
ENST00000512621.5:n.333-872T=
ENST00000512659.5:c.*32-872T= ENSP00000424650.1:n.*32-872T=
ENST00000512991.5:n.543-872T=
ENST00000626055.2:c.*32-872T= ENSP00000487496.1:n.*32-872T=
NM_000671.4:c.345-872T= MANE Select NP_000662.3:n.345-872T=