Canonical Allele Identifier: CA1261196301
Community Standard Title: NM_080916.3(DGUOK):c.425G= (p.Arg142=)
Gene: DGUOK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73946888G= , CM000664.2:g.73946888G= GRCh38
NC_000002.11:g.74174015G= , CM000664.1:g.74174015G= GRCh37
NC_000002.10:g.74027523G= NCBI36
NG_008044.1:g.25063G=

Transcript Alleles

HGVS Amino-acid Change
NM_080916.3:c.425G= MANE Select NP_550438.1:p.Arg142=
ENST00000264093.9:c.425G= MANE Select ENSP00000264093.4:p.Arg142=
NM_001318859.1:c.425G= NP_001305788.1:p.Arg142=
NM_001318859.2:c.425G= NP_001305788.1:p.Arg142=
NM_001318860.1:c.134G= NP_001305789.1:p.Arg45=
NM_001318860.2:c.134G= NP_001305789.1:p.Arg45=
NM_001318861.1:c.134G= NP_001305790.1:p.Arg45=
NM_001318861.2:c.134G= NP_001305790.1:p.Arg45=
NM_001318862.1:c.134G= NP_001305791.1:p.Arg45=
NM_001318862.2:c.134G= NP_001305791.1:p.Arg45=
NM_001318863.1:c.134G= NP_001305792.1:p.Arg45=
NM_001318863.2:c.134G= NP_001305792.1:p.Arg45=
NM_080916.2:c.425G= NP_550438.1:p.Arg142=
NM_080918.2:c.425G= NP_550440.1:p.Arg142=
NM_080918.3:c.425G= NP_550440.1:p.Arg142=
NR_134893.1:n.397G=
NR_134893.2:n.343G=
NR_134894.1:n.397G=
NR_134894.2:n.343G=
NR_134895.1:n.228-11258G=
NR_134895.2:n.174-11258G=
NR_134896.1:n.397G=
NR_134896.2:n.343G=
NR_134897.1:n.483G=
NR_134897.2:n.429G=
NR_134898.1:n.397G=
NR_134898.2:n.343G=
ENST00000264093.8:c.425G= ENSP00000264093.4:p.Arg142=
ENST00000348222.3:c.425G= ENSP00000306964.3:p.Arg142=
ENST00000418996.5:c.*42G= ENSP00000408209.1:n.*42G=
ENST00000462551.1:n.330G=
ENST00000462685.1:n.412G=
ENST00000489796.5:n.442G=
ENST00000493055.1:n.428G=
ENST00000629438.2:c.*42G= ENSP00000487122.1:n.*42G=
XM_005264173.2:c.134G= XP_005264230.1:p.Arg45=
XM_005264174.1:c.134G= XP_005264231.1:p.Arg45=
XM_011532647.1:c.425G= XP_011530949.1:p.Arg142=
XM_011532647.2:c.425G= XP_011530949.1:p.Arg142=
XM_011532648.1:c.134G= XP_011530950.1:p.Arg45=
XM_024452739.1:c.134G= XP_024308507.1:p.Arg45=
XR_001738656.1:n.509G=
XR_244926.2:n.506G=
XR_244926.3:n.508G=