Canonical Allele Identifier: CA1479840680
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99077889_99077890delinsTG , CM000666.2:g.99077889_99077890delinsTG GRCh38
NC_000004.11:g.99999040_99999041delinsTG , CM000666.1:g.99999040_99999041delinsTG GRCh37
NC_000004.10:g.100218063_100218064delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.345-967_345-966delinsCA MANE Select ENSP00000296412.8:n.345-967_345-966delinsCA
ENST00000296412.13:c.345-967_345-966delinsCA ENSP00000296412.8:n.345-967_345-966delinsCA
ENST00000296412.12:c.345-967_345-966delinsCA ENSP00000296412.8:n.345-967_345-966delinsCA
ENST00000502590.5:c.*25-967_*25-966delinsCA ENSP00000422119.1:n.*25-967_*25-966delinsCA
ENST00000503130.5:c.306-967_306-966delinsCA ENSP00000427049.1:n.306-967_306-966delinsCA
ENST00000505652.1:c.*169-967_*169-966delinsCA ENSP00000421556.1:n.*169-967_*169-966delinsCA
ENST00000508511.5:n.362-967_362-966delinsCA
ENST00000512604.1:n.205-967_205-966delinsCA
ENST00000512621.5:n.333-967_333-966delinsCA
ENST00000512659.5:c.*32-967_*32-966delinsCA ENSP00000424650.1:n.*32-967_*32-966delinsCA
ENST00000512991.5:n.543-967_543-966delinsCA
ENST00000626055.2:c.*32-967_*32-966delinsCA ENSP00000487496.1:n.*32-967_*32-966delinsCA
NM_000671.4:c.345-967_345-966delinsCA MANE Select NP_000662.3:n.345-967_345-966delinsCA