Canonical Allele Identifier: CA1479840657

Gene: ADH5

Linked Data

• dbSNP Id: rs1727957556

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99077847_99077849del , CM000666.2:g.99077847_99077849del	GRCh38
NC_000004.11:g.99998998_99999000del , CM000666.1:g.99998998_99999000del	GRCh37
NC_000004.10:g.100218021_100218023del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-922_345-920del MANE Select	ENSP00000296412.8:n.345-922_345-920del
ENST00000296412.13:c.345-922_345-920del	ENSP00000296412.8:n.345-922_345-920del
ENST00000296412.12:c.345-922_345-920del	ENSP00000296412.8:n.345-922_345-920del
ENST00000502590.5:c.*25-922_*25-920del	ENSP00000422119.1:n.*25-922_*25-920del
ENST00000503130.5:c.306-922_306-920del	ENSP00000427049.1:n.306-922_306-920del
ENST00000505652.1:c.*169-922_*169-920del	ENSP00000421556.1:n.*169-922_*169-920del
ENST00000508511.5:n.362-922_362-920del
ENST00000512604.1:n.205-922_205-920del
ENST00000512621.5:n.333-922_333-920del
ENST00000512659.5:c.*32-922_*32-920del	ENSP00000424650.1:n.*32-922_*32-920del
ENST00000512991.5:n.543-922_543-920del
ENST00000626055.2:c.*32-922_*32-920del	ENSP00000487496.1:n.*32-922_*32-920del
NM_000671.4:c.345-922_345-920del MANE Select	NP_000662.3:n.345-922_345-920del