Canonical Allele Identifier: CA1479863663

Gene: ADH4

Linked Data

• dbSNP Id: rs1185780394

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99134379_99134380insTTAT , CM000666.2:g.99134379_99134380insTTAT	GRCh38
NC_000004.11:g.100055530_100055531insTTAT , CM000666.1:g.100055530_100055531insTTAT	GRCh37
NC_000004.10:g.100274553_100274554insTTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.582+2087_582+2088insTAAA MANE Select	ENSP00000265512.7:n.582+2087_582+2088insT...
ENST00000265512.11:c.582+2087_582+2088insTAAA	ENSP00000265512.7:n.582+2087_582+2088insT...
ENST00000503416.5:n.595+2087_595+2088insTAAA
ENST00000504125.1:c.528+2087_528+2088insTAAA	ENSP00000427525.1:n.528+2087_528+2088insT...
ENST00000505590.5:c.639+2087_639+2088insTAAA	ENSP00000425416.1:n.639+2087_639+2088insT...
ENST00000506705.5:c.*556+2087_*556+2088insTAAA	ENSP00000426667.1:n.*556+2087_*556+2088in...
ENST00000508393.5:c.639+2087_639+2088insTAAA	ENSP00000424630.1:n.639+2087_639+2088insT...
ENST00000509471.5:c.72+2087_72+2088insTAAA	ENSP00000424583.1:n.72+2087_72+2088insTAA...
ENST00000512499.5:c.639+2087_639+2088insTAAA	ENSP00000423571.1:n.639+2087_639+2088insT...
ENST00000629236.2:c.582+2087_582+2088insTAAA	ENSP00000486450.1:n.582+2087_582+2088insT...
NM_000670.3:c.582+2087_582+2088insTAAA	NP_000661.2:n.582+2087_582+2088insTAAA
NM_000670.4:c.582+2087_582+2088insTAAA	NP_000661.2:n.582+2087_582+2088insTAAA
NM_001306171.1:c.639+2087_639+2088insTAAA	NP_001293100.1:n.639+2087_639+2088insTAAA...
NM_001306172.1:c.639+2087_639+2088insTAAA	NP_001293101.1:n.639+2087_639+2088insTAAA...
NR_037884.1:n.679+574_679+575insTTAT
XR_938685.1:n.810+2087_810+2088insTAAA
XR_938686.1:n.801+2087_801+2088insTAAA
XR_938687.1:n.674+2087_674+2088insTAAA
NM_000670.5:c.582+2087_582+2088insTAAA MANE Select	NP_000661.2:n.582+2087_582+2088insTAAA
NM_001306171.2:c.639+2087_639+2088insTAAA	NP_001293100.1:n.639+2087_639+2088insTAAA...
NM_001306172.2:c.639+2087_639+2088insTAAA	NP_001293101.1:n.639+2087_639+2088insTAAA...