Canonical Allele Identifier: CA347301901

Gene: DGUOK DGUOK-AS1

Linked Data

• gnomAD v4: 2-73958172-T-C
• MyVariant Identifiers: chr2:g.74185299T>C (hg19) ; chr2:g.73958172T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73958172T>C , CM000664.2:g.73958172T>C	GRCh38
NC_000002.11:g.74185299T>C , CM000664.1:g.74185299T>C	GRCh37
NC_000002.10:g.74038807T>C	NCBI36
NG_008044.1:g.36347T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.734T>C (DGUOK) MANE Select	ENSP00000264093.4:p.Ile245Thr
ENST00000264093.8:c.734T>C (DGUOK)	ENSP00000264093.4:p.Ile245Thr
ENST00000348222.3:c.470T>C (DGUOK)	ENSP00000306964.3:p.Ile157Thr
ENST00000418996.5:c.*87T>C (DGUOK)	ENSP00000408209.1:n.*87T>C
ENST00000462685.1:n.563T>C (DGUOK)
ENST00000489796.5:n.619T>C (DGUOK)
ENST00000629438.2:c.*351T>C (DGUOK)	ENSP00000487122.1:n.*351T>C
NM_080916.2:c.734T>C (DGUOK)	NP_550438.1:p.Ile245Thr
NM_080918.2:c.470T>C (DGUOK)	NP_550440.1:p.Ile157Thr
NR_104029.1:n.367A>G (DGUOK-AS1)
NR_104030.1:n.341A>G (DGUOK-AS1)
XM_005264173.2:c.443T>C (DGUOK)	XP_005264230.1:p.Ile148Thr
XM_005264174.1:c.443T>C (DGUOK)	XP_005264231.1:p.Ile148Thr
XM_011532647.1:c.716T>C (DGUOK)	XP_011530949.1:p.Ile239Thr
XM_011532648.1:c.425T>C (DGUOK)	XP_011530950.1:p.Ile142Thr
XR_244926.2:n.699T>C (DGUOK)
NM_001318859.1:c.452T>C (DGUOK)	NP_001305788.1:p.Ile151Thr
NM_001318860.1:c.443T>C (DGUOK)	NP_001305789.1:p.Ile148Thr
NM_001318861.1:c.443T>C (DGUOK)	NP_001305790.1:p.Ile148Thr
NM_001318862.1:c.425T>C (DGUOK)	NP_001305791.1:p.Ile142Thr
NM_001318863.1:c.425T>C (DGUOK)	NP_001305792.1:p.Ile142Thr
NR_134893.1:n.442T>C (DGUOK)
NR_134894.1:n.590T>C (DGUOK)
NR_134895.1:n.254T>C (DGUOK)
NR_134896.1:n.424T>C (DGUOK)
NR_134897.1:n.634T>C (DGUOK)
NR_134898.1:n.558T>C (DGUOK)
XM_011532647.2:c.716T>C (DGUOK)	XP_011530949.1:p.Ile239Thr
XM_024452739.1:c.443T>C (DGUOK)	XP_024308507.1:p.Ile148Thr
XR_001738656.1:n.670T>C (DGUOK)
XR_244926.3:n.701T>C (DGUOK)
NM_080916.3:c.734T>C (DGUOK) MANE Select	NP_550438.1:p.Ile245Thr
NM_001318859.2:c.452T>C (DGUOK)	NP_001305788.1:p.Ile151Thr
NM_001318860.2:c.443T>C (DGUOK)	NP_001305789.1:p.Ile148Thr
NM_001318861.2:c.443T>C (DGUOK)	NP_001305790.1:p.Ile148Thr
NM_001318862.2:c.425T>C (DGUOK)	NP_001305791.1:p.Ile142Thr
NM_001318863.2:c.425T>C (DGUOK)	NP_001305792.1:p.Ile142Thr
NM_080918.3:c.470T>C (DGUOK)	NP_550440.1:p.Ile157Thr
NR_134893.2:n.388T>C (DGUOK)
NR_134894.2:n.536T>C (DGUOK)
NR_134895.2:n.200T>C (DGUOK)
NR_134896.2:n.370T>C (DGUOK)
NR_134897.2:n.580T>C (DGUOK)
NR_134898.2:n.504T>C (DGUOK)