Canonical Allele Identifier: CA1479863691
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99134436_99134437delinsTA , CM000666.2:g.99134436_99134437delinsTA GRCh38
NC_000004.11:g.100055587_100055588delinsTA , CM000666.1:g.100055587_100055588delinsTA GRCh37
NC_000004.10:g.100274610_100274611delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.582+2029_582+2030delinsTA MANE Select ENSP00000265512.7:n.582+2029_582+2030deli...
ENST00000265512.11:c.582+2029_582+2030delinsTA ENSP00000265512.7:n.582+2029_582+2030deli...
ENST00000503416.5:n.595+2029_595+2030delinsTA
ENST00000504125.1:c.528+2029_528+2030delinsTA ENSP00000427525.1:n.528+2029_528+2030deli...
ENST00000505590.5:c.639+2029_639+2030delinsTA ENSP00000425416.1:n.639+2029_639+2030deli...
ENST00000506705.5:c.*556+2029_*556+2030delinsTA ENSP00000426667.1:n.*556+2029_*556+2030de...
ENST00000508393.5:c.639+2029_639+2030delinsTA ENSP00000424630.1:n.639+2029_639+2030deli...
ENST00000509471.5:c.72+2029_72+2030delinsTA ENSP00000424583.1:n.72+2029_72+2030delins...
ENST00000512499.5:c.639+2029_639+2030delinsTA ENSP00000423571.1:n.639+2029_639+2030deli...
ENST00000629236.2:c.582+2029_582+2030delinsTA ENSP00000486450.1:n.582+2029_582+2030deli...
NM_000670.3:c.582+2029_582+2030delinsTA NP_000661.2:n.582+2029_582+2030delinsTA
NM_000670.4:c.582+2029_582+2030delinsTA NP_000661.2:n.582+2029_582+2030delinsTA
NM_001306171.1:c.639+2029_639+2030delinsTA NP_001293100.1:n.639+2029_639+2030delinsT...
NM_001306172.1:c.639+2029_639+2030delinsTA NP_001293101.1:n.639+2029_639+2030delinsT...
NR_037884.1:n.679+631_679+632delinsTA
XR_938685.1:n.810+2029_810+2030delinsTA
XR_938686.1:n.801+2029_801+2030delinsTA
XR_938687.1:n.674+2029_674+2030delinsTA
NM_000670.5:c.582+2029_582+2030delinsTA MANE Select NP_000661.2:n.582+2029_582+2030delinsTA
NM_001306171.2:c.639+2029_639+2030delinsTA NP_001293100.1:n.639+2029_639+2030delinsT...
NM_001306172.2:c.639+2029_639+2030delinsTA NP_001293101.1:n.639+2029_639+2030delinsT...