Canonical Allele Identifier: CA2602451397

Gene: ADH5

Linked Data

• gnomAD v3: 4-99078220-CTCACTA-C
• gnomAD v4: 4-99078220-CTCACTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99078222_99078227del , CM000666.2:g.99078222_99078227del	GRCh38
NC_000004.11:g.99999373_99999378del , CM000666.1:g.99999373_99999378del	GRCh37
NC_000004.10:g.100218396_100218401del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296412.14:c.345-1303_345-1298del MANE Select	ENSP00000296412.8:n.345-1303_345-1298del
ENST00000296412.13:c.345-1303_345-1298del	ENSP00000296412.8:n.345-1303_345-1298del
ENST00000296412.12:c.345-1303_345-1298del	ENSP00000296412.8:n.345-1303_345-1298del
ENST00000502590.5:c.*25-1303_*25-1298del	ENSP00000422119.1:n.*25-1303_*25-1298del
ENST00000503130.5:c.306-1303_306-1298del	ENSP00000427049.1:n.306-1303_306-1298del
ENST00000505652.1:c.*169-1303_*169-1298del	ENSP00000421556.1:n.*169-1303_*169-1298del
ENST00000508511.5:n.362-1303_362-1298del
ENST00000512604.1:n.205-1303_205-1298del
ENST00000512621.5:n.333-1303_333-1298del
ENST00000512659.5:c.*32-1303_*32-1298del	ENSP00000424650.1:n.*32-1303_*32-1298del
ENST00000512991.5:n.543-1303_543-1298del
ENST00000626055.2:c.*32-1303_*32-1298del	ENSP00000487496.1:n.*32-1303_*32-1298del
NM_000671.4:c.345-1303_345-1298del MANE Select	NP_000662.3:n.345-1303_345-1298del