Canonical Allele Identifier: CA347298732

Gene: DGUOK

Linked Data

• MyVariant Identifiers: chr2:g.74173849T>G (hg19) ; chr2:g.73946722T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73946722T>G , CM000664.2:g.73946722T>G	GRCh38
NC_000002.11:g.74173849T>G , CM000664.1:g.74173849T>G	GRCh37
NC_000002.10:g.74027357T>G	NCBI36
NG_008044.1:g.24897T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.259T>G MANE Select	ENSP00000264093.4:p.Cys87Gly
ENST00000264093.8:c.259T>G	ENSP00000264093.4:p.Cys87Gly
ENST00000348222.3:c.259T>G	ENSP00000306964.3:p.Cys87Gly
ENST00000418996.5:c.146T>G	ENSP00000408209.1:p.Leu49Arg
ENST00000462551.1:n.164T>G
ENST00000462685.1:n.246T>G
ENST00000489796.5:n.276T>G
ENST00000493055.1:n.262T>G
ENST00000629438.2:c.146T>G	ENSP00000487122.1:p.Leu49Arg
NM_080916.2:c.259T>G	NP_550438.1:p.Cys87Gly
NM_080918.2:c.259T>G	NP_550440.1:p.Cys87Gly
XM_005264173.2:c.-33T>G	XP_005264230.1:n.-33T>G
XM_005264174.1:c.-33T>G	XP_005264231.1:n.-33T>G
XM_011532647.1:c.259T>G	XP_011530949.1:p.Cys87Gly
XM_011532648.1:c.-33T>G	XP_011530950.1:n.-33T>G
XR_244926.2:n.340T>G
NM_001318859.1:c.259T>G	NP_001305788.1:p.Cys87Gly
NM_001318860.1:c.-33T>G	NP_001305789.1:n.-33T>G
NM_001318861.1:c.-33T>G	NP_001305790.1:n.-33T>G
NM_001318862.1:c.-33T>G	NP_001305791.1:n.-33T>G
NM_001318863.1:c.-33T>G	NP_001305792.1:n.-33T>G
NR_134893.1:n.231T>G
NR_134894.1:n.231T>G
NR_134895.1:n.228-11424T>G
NR_134896.1:n.231T>G
NR_134897.1:n.317T>G
NR_134898.1:n.231T>G
XM_011532647.2:c.259T>G	XP_011530949.1:p.Cys87Gly
XM_024452739.1:c.-33T>G	XP_024308507.1:n.-33T>G
XR_001738656.1:n.343T>G
XR_244926.3:n.342T>G
NM_080916.3:c.259T>G MANE Select	NP_550438.1:p.Cys87Gly
NM_001318859.2:c.259T>G	NP_001305788.1:p.Cys87Gly
NM_001318860.2:c.-33T>G	NP_001305789.1:n.-33T>G
NM_001318861.2:c.-33T>G	NP_001305790.1:n.-33T>G
NM_001318862.2:c.-33T>G	NP_001305791.1:n.-33T>G
NM_001318863.2:c.-33T>G	NP_001305792.1:n.-33T>G
NM_080918.3:c.259T>G	NP_550440.1:p.Cys87Gly
NR_134893.2:n.177T>G
NR_134894.2:n.177T>G
NR_134895.2:n.174-11424T>G
NR_134896.2:n.177T>G
NR_134897.2:n.263T>G
NR_134898.2:n.177T>G