Canonical Allele Identifier: CA347302098

Gene: DGUOK DGUOK-AS1

Linked Data

• MyVariant Identifiers: chr2:g.74185847T>C (hg19) ; chr2:g.73958720T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73958720T>C , CM000664.2:g.73958720T>C	GRCh38
NC_000002.11:g.74185847T>C , CM000664.1:g.74185847T>C	GRCh37
NC_000002.10:g.74039355T>C	NCBI36
NG_008044.1:g.36895T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.818T>C (DGUOK) MANE Select	ENSP00000264093.4:p.Phe273Ser
ENST00000264093.8:c.818T>C (DGUOK)	ENSP00000264093.4:p.Phe273Ser
ENST00000348222.3:c.554T>C (DGUOK)	ENSP00000306964.3:p.Phe185Ser
ENST00000418996.5:c.*171T>C (DGUOK)	ENSP00000408209.1:n.*171T>C
ENST00000462685.1:n.647T>C (DGUOK)
ENST00000629438.2:c.*435T>C (DGUOK)	ENSP00000487122.1:n.*435T>C
NM_080916.2:c.818T>C (DGUOK)	NP_550438.1:p.Phe273Ser
NM_080918.2:c.554T>C (DGUOK)	NP_550440.1:p.Phe185Ser
NR_104029.1:n.332-513A>G (DGUOK-AS1)
NR_104030.1:n.306-513A>G (DGUOK-AS1)
XM_005264173.2:c.527T>C (DGUOK)	XP_005264230.1:p.Phe176Ser
XM_005264174.1:c.527T>C (DGUOK)	XP_005264231.1:p.Phe176Ser
XM_011532647.1:c.800T>C (DGUOK)	XP_011530949.1:p.Phe267Ser
XM_011532648.1:c.509T>C (DGUOK)	XP_011530950.1:p.Phe170Ser
XR_244926.2:n.783T>C (DGUOK)
NM_001318859.1:c.536T>C (DGUOK)	NP_001305788.1:p.Phe179Ser
NM_001318860.1:c.527T>C (DGUOK)	NP_001305789.1:p.Phe176Ser
NM_001318861.1:c.527T>C (DGUOK)	NP_001305790.1:p.Phe176Ser
NM_001318862.1:c.509T>C (DGUOK)	NP_001305791.1:p.Phe170Ser
NM_001318863.1:c.509T>C (DGUOK)	NP_001305792.1:p.Phe170Ser
NR_134893.1:n.526T>C (DGUOK)
NR_134894.1:n.674T>C (DGUOK)
NR_134895.1:n.338T>C (DGUOK)
NR_134896.1:n.508T>C (DGUOK)
NR_134897.1:n.718T>C (DGUOK)
NR_134898.1:n.642T>C (DGUOK)
XM_011532647.2:c.800T>C (DGUOK)	XP_011530949.1:p.Phe267Ser
XM_024452739.1:c.527T>C (DGUOK)	XP_024308507.1:p.Phe176Ser
XR_001738656.1:n.754T>C (DGUOK)
XR_244926.3:n.785T>C (DGUOK)
NM_080916.3:c.818T>C (DGUOK) MANE Select	NP_550438.1:p.Phe273Ser
NM_001318859.2:c.536T>C (DGUOK)	NP_001305788.1:p.Phe179Ser
NM_001318860.2:c.527T>C (DGUOK)	NP_001305789.1:p.Phe176Ser
NM_001318861.2:c.527T>C (DGUOK)	NP_001305790.1:p.Phe176Ser
NM_001318862.2:c.509T>C (DGUOK)	NP_001305791.1:p.Phe170Ser
NM_001318863.2:c.509T>C (DGUOK)	NP_001305792.1:p.Phe170Ser
NM_080918.3:c.554T>C (DGUOK)	NP_550440.1:p.Phe185Ser
NR_134893.2:n.472T>C (DGUOK)
NR_134894.2:n.620T>C (DGUOK)
NR_134895.2:n.284T>C (DGUOK)
NR_134896.2:n.454T>C (DGUOK)
NR_134897.2:n.664T>C (DGUOK)
NR_134898.2:n.588T>C (DGUOK)