Canonical Allele Identifier: CA1139657119
Gene: DGUOK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73957243_73957246del , CM000664.2:g.73957243_73957246del GRCh38
NC_000002.11:g.74184370_74184373del , CM000664.1:g.74184370_74184373del GRCh37
NC_000002.10:g.74037878_74037881del NCBI36
NG_008044.1:g.35418_35421del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264093.9:c.707+3_707+6del
ENST00000264093.8:c.707+3_707+6del
ENST00000348222.3:c.444-903_444-900del ENSP00000306964.3:n.444-903_444-900del
ENST00000418996.5:c.*61-903_*61-900del ENSP00000408209.1:n.*61-903_*61-900del
ENST00000462685.1:n.537-903_537-900del
ENST00000489796.5:n.593-903_593-900del
ENST00000629438.2:c.*324+3_*324+6del
NM_080916.2:c.707+3_707+6del
NM_080918.2:c.444-903_444-900del NP_550440.1:n.444-903_444-900del
XM_005264173.2:c.416+3_416+6del
XM_005264174.1:c.416+3_416+6del
XM_011532647.1:c.689+3_689+6del
XM_011532648.1:c.398+3_398+6del
XR_244926.2:n.673-903_673-900del
NM_001318859.1:c.426-903_426-900del NP_001305788.1:n.426-903_426-900del
NM_001318860.1:c.416+3_416+6del
NM_001318861.1:c.416+3_416+6del
NM_001318862.1:c.398+3_398+6del
NM_001318863.1:c.398+3_398+6del
NR_134893.1:n.416-903_416-900del
NR_134894.1:n.564-903_564-900del
NR_134895.1:n.228-903_228-900del
NR_134896.1:n.398-903_398-900del
NR_134897.1:n.608-903_608-900del
NR_134898.1:n.531+3_531+6del
XM_011532647.2:c.689+3_689+6del
XM_024452739.1:c.416+3_416+6del
XR_001738656.1:n.643+3_643+6del
XR_244926.3:n.675-903_675-900del
NM_080916.3:c.707+3_707+6del
NM_001318859.2:c.426-903_426-900del NP_001305788.1:n.426-903_426-900del
NM_001318860.2:c.416+3_416+6del
NM_001318861.2:c.416+3_416+6del
NM_001318862.2:c.398+3_398+6del
NM_001318863.2:c.398+3_398+6del
NM_080918.3:c.444-903_444-900del NP_550440.1:n.444-903_444-900del
NR_134893.2:n.362-903_362-900del
NR_134894.2:n.510-903_510-900del
NR_134895.2:n.174-903_174-900del
NR_134896.2:n.344-903_344-900del
NR_134897.2:n.554-903_554-900del
NR_134898.2:n.477+3_477+6del