Canonical Allele Identifier: CA1065892435
Gene: ADH5 HGNC NCBI

Linked Data

dbSNP Id: rs1727960251

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99078004_99078005insAT , CM000666.2:g.99078004_99078005insAT GRCh38
NC_000004.11:g.99999155_99999156insAT , CM000666.1:g.99999155_99999156insAT GRCh37
NC_000004.10:g.100218178_100218179insAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296412.14:c.345-1082_345-1081insAT MANE Select ENSP00000296412.8:n.345-1082_345-1081insA...
ENST00000296412.13:c.345-1082_345-1081insAT ENSP00000296412.8:n.345-1082_345-1081insA...
ENST00000296412.12:c.345-1082_345-1081insAT ENSP00000296412.8:n.345-1082_345-1081insA...
ENST00000502590.5:c.*25-1082_*25-1081insAT ENSP00000422119.1:n.*25-1082_*25-1081insA...
ENST00000503130.5:c.306-1082_306-1081insAT ENSP00000427049.1:n.306-1082_306-1081insA...
ENST00000505652.1:c.*169-1082_*169-1081insAT ENSP00000421556.1:n.*169-1082_*169-1081in...
ENST00000508511.5:n.362-1082_362-1081insAT
ENST00000512604.1:n.205-1082_205-1081insAT
ENST00000512621.5:n.333-1082_333-1081insAT
ENST00000512659.5:c.*32-1082_*32-1081insAT ENSP00000424650.1:n.*32-1082_*32-1081insA...
ENST00000512991.5:n.543-1082_543-1081insAT
ENST00000626055.2:c.*32-1082_*32-1081insAT ENSP00000487496.1:n.*32-1082_*32-1081insA...
NM_000671.4:c.345-1082_345-1081insAT MANE Select NP_000662.3:n.345-1082_345-1081insAT