Canonical Allele Identifier: CA1479840828
Gene: ADH5 HGNC NCBI

Linked Data

dbSNP Id: rs1727961070

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99078057_99078106del , CM000666.2:g.99078057_99078106del GRCh38
NC_000004.11:g.99999208_99999257del , CM000666.1:g.99999208_99999257del GRCh37
NC_000004.10:g.100218231_100218280del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296412.14:c.345-1183_345-1134del MANE Select ENSP00000296412.8:n.345-1183_345-1134del
ENST00000296412.13:c.345-1183_345-1134del ENSP00000296412.8:n.345-1183_345-1134del
ENST00000296412.12:c.345-1183_345-1134del ENSP00000296412.8:n.345-1183_345-1134del
ENST00000502590.5:c.*25-1183_*25-1134del ENSP00000422119.1:n.*25-1183_*25-1134del
ENST00000503130.5:c.306-1183_306-1134del ENSP00000427049.1:n.306-1183_306-1134del
ENST00000505652.1:c.*169-1183_*169-1134del ENSP00000421556.1:n.*169-1183_*169-1134de...
ENST00000508511.5:n.362-1183_362-1134del
ENST00000512604.1:n.205-1183_205-1134del
ENST00000512621.5:n.333-1183_333-1134del
ENST00000512659.5:c.*32-1183_*32-1134del ENSP00000424650.1:n.*32-1183_*32-1134del
ENST00000512991.5:n.543-1183_543-1134del
ENST00000626055.2:c.*32-1183_*32-1134del ENSP00000487496.1:n.*32-1183_*32-1134del
NM_000671.4:c.345-1183_345-1134del MANE Select NP_000662.3:n.345-1183_345-1134del