Canonical Allele Identifier: CA2706767541

Gene: ADH5

Linked Data

• dbSNP Id: rs2110460541

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99078049_99078053del , CM000666.2:g.99078049_99078053del	GRCh38
NC_000004.11:g.99999200_99999204del , CM000666.1:g.99999200_99999204del	GRCh37
NC_000004.10:g.100218223_100218227del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-1126_345-1122del MANE Select	ENSP00000296412.8:n.345-1126_345-1122del
ENST00000296412.13:c.345-1126_345-1122del	ENSP00000296412.8:n.345-1126_345-1122del
ENST00000296412.12:c.345-1126_345-1122del	ENSP00000296412.8:n.345-1126_345-1122del
ENST00000502590.5:c.*25-1126_*25-1122del	ENSP00000422119.1:n.*25-1126_*25-1122del
ENST00000503130.5:c.306-1126_306-1122del	ENSP00000427049.1:n.306-1126_306-1122del
ENST00000505652.1:c.*169-1126_*169-1122del	ENSP00000421556.1:n.*169-1126_*169-1122del
ENST00000508511.5:n.362-1126_362-1122del
ENST00000512604.1:n.205-1126_205-1122del
ENST00000512621.5:n.333-1126_333-1122del
ENST00000512659.5:c.*32-1126_*32-1122del	ENSP00000424650.1:n.*32-1126_*32-1122del
ENST00000512991.5:n.543-1126_543-1122del
ENST00000626055.2:c.*32-1126_*32-1122del	ENSP00000487496.1:n.*32-1126_*32-1122del
NM_000671.4:c.345-1126_345-1122del MANE Select	NP_000662.3:n.345-1126_345-1122del