Canonical Allele Identifier: CA101603139

Gene: ADH5

Linked Data

• dbSNP Id: rs945153938
• MyVariant Identifiers: chr4:g.99998973A>T (hg19) ; chr4:g.99077822A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99077822A>T , CM000666.2:g.99077822A>T	GRCh38
NC_000004.11:g.99998973A>T , CM000666.1:g.99998973A>T	GRCh37
NC_000004.10:g.100217996A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-899T>A MANE Select	ENSP00000296412.8:n.345-899T>A
ENST00000296412.13:c.345-899T>A	ENSP00000296412.8:n.345-899T>A
ENST00000296412.12:c.345-899T>A	ENSP00000296412.8:n.345-899T>A
ENST00000502590.5:c.*25-899T>A	ENSP00000422119.1:n.*25-899T>A
ENST00000503130.5:c.306-899T>A	ENSP00000427049.1:n.306-899T>A
ENST00000505652.1:c.*169-899T>A	ENSP00000421556.1:n.*169-899T>A
ENST00000508511.5:n.362-899T>A
ENST00000512604.1:n.205-899T>A
ENST00000512621.5:n.333-899T>A
ENST00000512659.5:c.*32-899T>A	ENSP00000424650.1:n.*32-899T>A
ENST00000512991.5:n.543-899T>A
ENST00000626055.2:c.*32-899T>A	ENSP00000487496.1:n.*32-899T>A
NM_000671.4:c.345-899T>A MANE Select	NP_000662.3:n.345-899T>A