Canonical Allele Identifier: CA1479840690
Gene: ADH5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99077898_99077903delinsCAAGTT , CM000666.2:g.99077898_99077903delinsCAAGTT GRCh38
NC_000004.11:g.99999049_99999054delinsCAAGTT , CM000666.1:g.99999049_99999054delinsCAAGTT GRCh37
NC_000004.10:g.100218072_100218077delinsCAAGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296412.14:c.345-980_345-975delinsAACTTG MANE Select ENSP00000296412.8:n.345-980_345-975delinsAACTTG
ENST00000296412.13:c.345-980_345-975delinsAACTTG ENSP00000296412.8:n.345-980_345-975delinsAACTTG
ENST00000296412.12:c.345-980_345-975delinsAACTTG ENSP00000296412.8:n.345-980_345-975delinsAACTTG
ENST00000502590.5:c.*25-980_*25-975delinsAACTTG ENSP00000422119.1:n.*25-980_*25-975delinsAACTTG
ENST00000503130.5:c.306-980_306-975delinsAACTTG ENSP00000427049.1:n.306-980_306-975delinsAACTTG
ENST00000505652.1:c.*169-980_*169-975delinsAACTTG ENSP00000421556.1:n.*169-980_*169-975delinsAACTTG
ENST00000508511.5:n.362-980_362-975delinsAACTTG
ENST00000512604.1:n.205-980_205-975delinsAACTTG
ENST00000512621.5:n.333-980_333-975delinsAACTTG
ENST00000512659.5:c.*32-980_*32-975delinsAACTTG ENSP00000424650.1:n.*32-980_*32-975delinsAACTTG
ENST00000512991.5:n.543-980_543-975delinsAACTTG
ENST00000626055.2:c.*32-980_*32-975delinsAACTTG ENSP00000487496.1:n.*32-980_*32-975delinsAACTTG
NM_000671.4:c.345-980_345-975delinsAACTTG MANE Select NP_000662.3:n.345-980_345-975delinsAACTTG