Canonical Allele Identifier: CA347301849
Gene: DGUOK HGNC NCBI
DGUOK-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73958150C>T , CM000664.2:g.73958150C>T GRCh38
NC_000002.11:g.74185277C>T , CM000664.1:g.74185277C>T GRCh37
NC_000002.10:g.74038785C>T NCBI36
NG_008044.1:g.36325C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264093.9:c.712C>T (DGUOK) MANE Select ENSP00000264093.4:p.His238Tyr
ENST00000264093.8:c.712C>T (DGUOK) ENSP00000264093.4:p.His238Tyr
ENST00000348222.3:c.448C>T (DGUOK) ENSP00000306964.3:p.His150Tyr
ENST00000418996.5:c.*65C>T (DGUOK) ENSP00000408209.1:n.*65C>T
ENST00000462685.1:n.541C>T (DGUOK)
ENST00000489796.5:n.597C>T (DGUOK)
ENST00000629438.2:c.*329C>T (DGUOK) ENSP00000487122.1:n.*329C>T
NM_080916.2:c.712C>T (DGUOK) NP_550438.1:p.His238Tyr
NM_080918.2:c.448C>T (DGUOK) NP_550440.1:p.His150Tyr
NR_104029.1:n.389G>A (DGUOK-AS1)
NR_104030.1:n.363G>A (DGUOK-AS1)
XM_005264173.2:c.421C>T (DGUOK) XP_005264230.1:p.His141Tyr
XM_005264174.1:c.421C>T (DGUOK) XP_005264231.1:p.His141Tyr
XM_011532647.1:c.694C>T (DGUOK) XP_011530949.1:p.His232Tyr
XM_011532648.1:c.403C>T (DGUOK) XP_011530950.1:p.His135Tyr
XR_244926.2:n.677C>T (DGUOK)
NM_001318859.1:c.430C>T (DGUOK) NP_001305788.1:p.His144Tyr
NM_001318860.1:c.421C>T (DGUOK) NP_001305789.1:p.His141Tyr
NM_001318861.1:c.421C>T (DGUOK) NP_001305790.1:p.His141Tyr
NM_001318862.1:c.403C>T (DGUOK) NP_001305791.1:p.His135Tyr
NM_001318863.1:c.403C>T (DGUOK) NP_001305792.1:p.His135Tyr
NR_134893.1:n.420C>T (DGUOK)
NR_134894.1:n.568C>T (DGUOK)
NR_134895.1:n.232C>T (DGUOK)
NR_134896.1:n.402C>T (DGUOK)
NR_134897.1:n.612C>T (DGUOK)
NR_134898.1:n.536C>T (DGUOK)
XM_011532647.2:c.694C>T (DGUOK) XP_011530949.1:p.His232Tyr
XM_024452739.1:c.421C>T (DGUOK) XP_024308507.1:p.His141Tyr
XR_001738656.1:n.648C>T (DGUOK)
XR_244926.3:n.679C>T (DGUOK)
NM_080916.3:c.712C>T (DGUOK) MANE Select NP_550438.1:p.His238Tyr
NM_001318859.2:c.430C>T (DGUOK) NP_001305788.1:p.His144Tyr
NM_001318860.2:c.421C>T (DGUOK) NP_001305789.1:p.His141Tyr
NM_001318861.2:c.421C>T (DGUOK) NP_001305790.1:p.His141Tyr
NM_001318862.2:c.403C>T (DGUOK) NP_001305791.1:p.His135Tyr
NM_001318863.2:c.403C>T (DGUOK) NP_001305792.1:p.His135Tyr
NM_080918.3:c.448C>T (DGUOK) NP_550440.1:p.His150Tyr
NR_134893.2:n.366C>T (DGUOK)
NR_134894.2:n.514C>T (DGUOK)
NR_134895.2:n.178C>T (DGUOK)
NR_134896.2:n.348C>T (DGUOK)
NR_134897.2:n.558C>T (DGUOK)
NR_134898.2:n.482C>T (DGUOK)