Canonical Allele Identifier: CA1479840827
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99078056_99078106delinsTAAATAAAATAAACACTATAATTGCTTTTTTTGAGACAGCCCAGGCTGGAG , CM000666.2:g.99078056_99078106delinsTAAATAAAATAAACACTATAATTGCTTTTTTTGAGACAGCCCAGGCTGGAG GRCh38
NC_000004.11:g.99999207_99999257delinsTAAATAAAATAAACACTATAATTGCTTTTTTTGAGACAGCCCAGGCTGGAG , CM000666.1:g.99999207_99999257delinsTAAATAAAATAAACACTATAATTGCTTTTTTTGAGACAGCCCAGGCTGGAG GRCh37
NC_000004.10:g.100218230_100218280delinsTAAATAAAATAAACACTATAATTGCTTTTTTTGAGACAGCCCAGGCTGGAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296412.14:c.345-1183_345-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA MANE Select ENSP00000296412.8:n.345-1183_345-1133deli...
ENST00000296412.13:c.345-1183_345-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000296412.8:n.345-1183_345-1133deli...
ENST00000296412.12:c.345-1183_345-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000296412.8:n.345-1183_345-1133deli...
ENST00000502590.5:c.*25-1183_*25-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000422119.1:n.*25-1183_*25-1133deli...
ENST00000503130.5:c.306-1183_306-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000427049.1:n.306-1183_306-1133deli...
ENST00000505652.1:c.*169-1183_*169-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000421556.1:n.*169-1183_*169-1133de...
ENST00000508511.5:n.362-1183_362-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA
ENST00000512604.1:n.205-1183_205-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA
ENST00000512621.5:n.333-1183_333-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA
ENST00000512659.5:c.*32-1183_*32-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000424650.1:n.*32-1183_*32-1133deli...
ENST00000512991.5:n.543-1183_543-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA
ENST00000626055.2:c.*32-1183_*32-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA ENSP00000487496.1:n.*32-1183_*32-1133deli...
NM_000671.4:c.345-1183_345-1133delinsCTCCAGCCTGGGCTGTCTCAAAAAAAGCAATTATAGTGTTTATTTTATTTA MANE Select NP_000662.3:n.345-1183_345-1133delinsCTCC...