Canonical Allele Identifier: CA347302030

Gene: DGUOK DGUOK-AS1

Linked Data

• MyVariant Identifiers: chr2:g.74185358G>T (hg19) ; chr2:g.73958231G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73958231G>T , CM000664.2:g.73958231G>T	GRCh38
NC_000002.11:g.74185358G>T , CM000664.1:g.74185358G>T	GRCh37
NC_000002.10:g.74038866G>T	NCBI36
NG_008044.1:g.36406G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.793G>T (DGUOK) MANE Select	ENSP00000264093.4:p.Asp265Tyr
ENST00000264093.8:c.793G>T (DGUOK)	ENSP00000264093.4:p.Asp265Tyr
ENST00000348222.3:c.529G>T (DGUOK)	ENSP00000306964.3:p.Asp177Tyr
ENST00000418996.5:c.*146G>T (DGUOK)	ENSP00000408209.1:n.*146G>T
ENST00000462685.1:n.622G>T (DGUOK)
ENST00000489796.5:n.678G>T (DGUOK)
ENST00000629438.2:c.*410G>T (DGUOK)	ENSP00000487122.1:n.*410G>T
NM_080916.2:c.793G>T (DGUOK)	NP_550438.1:p.Asp265Tyr
NM_080918.2:c.529G>T (DGUOK)	NP_550440.1:p.Asp177Tyr
NR_104029.1:n.332-24C>A (DGUOK-AS1)
NR_104030.1:n.306-24C>A (DGUOK-AS1)
XM_005264173.2:c.502G>T (DGUOK)	XP_005264230.1:p.Asp168Tyr
XM_005264174.1:c.502G>T (DGUOK)	XP_005264231.1:p.Asp168Tyr
XM_011532647.1:c.775G>T (DGUOK)	XP_011530949.1:p.Asp259Tyr
XM_011532648.1:c.484G>T (DGUOK)	XP_011530950.1:p.Asp162Tyr
XR_244926.2:n.758G>T (DGUOK)
NM_001318859.1:c.511G>T (DGUOK)	NP_001305788.1:p.Asp171Tyr
NM_001318860.1:c.502G>T (DGUOK)	NP_001305789.1:p.Asp168Tyr
NM_001318861.1:c.502G>T (DGUOK)	NP_001305790.1:p.Asp168Tyr
NM_001318862.1:c.484G>T (DGUOK)	NP_001305791.1:p.Asp162Tyr
NM_001318863.1:c.484G>T (DGUOK)	NP_001305792.1:p.Asp162Tyr
NR_134893.1:n.501G>T (DGUOK)
NR_134894.1:n.649G>T (DGUOK)
NR_134895.1:n.313G>T (DGUOK)
NR_134896.1:n.483G>T (DGUOK)
NR_134897.1:n.693G>T (DGUOK)
NR_134898.1:n.617G>T (DGUOK)
XM_011532647.2:c.775G>T (DGUOK)	XP_011530949.1:p.Asp259Tyr
XM_024452739.1:c.502G>T (DGUOK)	XP_024308507.1:p.Asp168Tyr
XR_001738656.1:n.729G>T (DGUOK)
XR_244926.3:n.760G>T (DGUOK)
NM_080916.3:c.793G>T (DGUOK) MANE Select	NP_550438.1:p.Asp265Tyr
NM_001318859.2:c.511G>T (DGUOK)	NP_001305788.1:p.Asp171Tyr
NM_001318860.2:c.502G>T (DGUOK)	NP_001305789.1:p.Asp168Tyr
NM_001318861.2:c.502G>T (DGUOK)	NP_001305790.1:p.Asp168Tyr
NM_001318862.2:c.484G>T (DGUOK)	NP_001305791.1:p.Asp162Tyr
NM_001318863.2:c.484G>T (DGUOK)	NP_001305792.1:p.Asp162Tyr
NM_080918.3:c.529G>T (DGUOK)	NP_550440.1:p.Asp177Tyr
NR_134893.2:n.447G>T (DGUOK)
NR_134894.2:n.595G>T (DGUOK)
NR_134895.2:n.259G>T (DGUOK)
NR_134896.2:n.429G>T (DGUOK)
NR_134897.2:n.639G>T (DGUOK)
NR_134898.2:n.563G>T (DGUOK)