Canonical Allele Identifier: CA50404364

Gene: DGUOK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73939002C>T , CM000664.2:g.73939002C>T	GRCh38
NC_000002.11:g.74166129C>T , CM000664.1:g.74166129C>T	GRCh37
NC_000002.10:g.74019637C>T	NCBI36
NG_008044.1:g.17177C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_080916.3:c.235C>T MANE Select	NP_550438.1:p.Gln79Ter
ENST00000264093.9:c.235C>T MANE Select	ENSP00000264093.4:p.Gln79Ter
NM_001318859.1:c.235C>T	NP_001305788.1:p.Gln79Ter
NM_001318859.2:c.235C>T	NP_001305788.1:p.Gln79Ter
NM_001318860.1:c.-36-7717C>T	NP_001305789.1:n.-36-7717C>T
NM_001318860.2:c.-36-7717C>T	NP_001305789.1:n.-36-7717C>T
NM_001318861.1:c.-37+6319C>T	NP_001305790.1:n.-37+6319C>T
NM_001318861.2:c.-37+6319C>T	NP_001305790.1:n.-37+6319C>T
NM_001318862.1:c.-37+6319C>T	NP_001305791.1:n.-37+6319C>T
NM_001318862.2:c.-37+6319C>T	NP_001305791.1:n.-37+6319C>T
NM_001318863.1:c.-36-7717C>T	NP_001305792.1:n.-36-7717C>T
NM_001318863.2:c.-36-7717C>T	NP_001305792.1:n.-36-7717C>T
NM_080916.2:c.235C>T	NP_550438.1:p.Gln79Ter
NM_080918.2:c.235C>T	NP_550440.1:p.Gln79Ter
NM_080918.3:c.235C>T	NP_550440.1:p.Gln79Ter
NR_134893.1:n.228-7717C>T
NR_134893.2:n.174-7717C>T
NR_134894.1:n.228-7717C>T
NR_134894.2:n.174-7717C>T
NR_134895.1:n.227+11950C>T
NR_134895.2:n.173+11950C>T
NR_134896.1:n.228-7717C>T
NR_134896.2:n.174-7717C>T
NR_134897.1:n.313+6319C>T
NR_134897.2:n.259+6319C>T
NR_134898.1:n.228-7717C>T
NR_134898.2:n.174-7717C>T
ENST00000264093.8:c.235C>T	ENSP00000264093.4:p.Gln79Ter
ENST00000348222.3:c.235C>T	ENSP00000306964.3:p.Gln79Ter
ENST00000418996.5:c.143-7717C>T	ENSP00000408209.1:n.143-7717C>T
ENST00000462551.1:n.161-7717C>T
ENST00000462685.1:n.242+6319C>T
ENST00000489796.5:n.252C>T
ENST00000493055.1:n.238C>T
ENST00000629438.2:c.143-7717C>T	ENSP00000487122.1:n.143-7717C>T
XM_005264173.2:c.-36-7717C>T	XP_005264230.1:n.-36-7717C>T
XM_005264174.1:c.-37+6319C>T	XP_005264231.1:n.-37+6319C>T
XM_011532647.1:c.235C>T	XP_011530949.1:p.Gln79Ter
XM_011532647.2:c.235C>T	XP_011530949.1:p.Gln79Ter
XM_011532648.1:c.-37+6319C>T	XP_011530950.1:n.-37+6319C>T
XM_024452739.1:c.-57C>T	XP_024308507.1:n.-57C>T
XR_001738656.1:n.319C>T
XR_244926.2:n.316C>T
XR_244926.3:n.318C>T