Canonical Allele Identifier: CA101603140

Gene: ADH5

Linked Data

• dbSNP Id: rs149434070
• gnomAD v2: 4-99999002-C-T
• gnomAD v3: 4-99077851-C-T
• gnomAD v4: 4-99077851-C-T
• MyVariant Identifiers: chr4:g.99999002C>T (hg19) ; chr4:g.99077851C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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