Canonical Allele Identifier: CA1261201259

Gene: DGUOK

Linked Data

• dbSNP Id: rs1683247002

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73957961_73957964dup , CM000664.2:g.73957961_73957964dup	GRCh38
NC_000002.11:g.74185088_74185091dup , CM000664.1:g.74185088_74185091dup	GRCh37
NC_000002.10:g.74038596_74038599dup	NCBI36
NG_008044.1:g.36136_36139dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.708-185_708-182dup MANE Select	ENSP00000264093.4:n.708-185_708-182dup
ENST00000264093.8:c.708-185_708-182dup	ENSP00000264093.4:n.708-185_708-182dup
ENST00000348222.3:c.444-185_444-182dup	ENSP00000306964.3:n.444-185_444-182dup
ENST00000418996.5:c.*61-185_*61-182dup	ENSP00000408209.1:n.*61-185_*61-182dup
ENST00000462685.1:n.537-185_537-182dup
ENST00000489796.5:n.593-185_593-182dup
ENST00000629438.2:c.*325-185_*325-182dup	ENSP00000487122.1:n.*325-185_*325-182dup
NM_080916.2:c.708-185_708-182dup	NP_550438.1:n.708-185_708-182dup
NM_080918.2:c.444-185_444-182dup	NP_550440.1:n.444-185_444-182dup
XM_005264173.2:c.417-185_417-182dup	XP_005264230.1:n.417-185_417-182dup
XM_005264174.1:c.417-185_417-182dup	XP_005264231.1:n.417-185_417-182dup
XM_011532647.1:c.690-185_690-182dup	XP_011530949.1:n.690-185_690-182dup
XM_011532648.1:c.399-185_399-182dup	XP_011530950.1:n.399-185_399-182dup
XR_244926.2:n.673-185_673-182dup
NM_001318859.1:c.426-185_426-182dup	NP_001305788.1:n.426-185_426-182dup
NM_001318860.1:c.417-185_417-182dup	NP_001305789.1:n.417-185_417-182dup
NM_001318861.1:c.417-185_417-182dup	NP_001305790.1:n.417-185_417-182dup
NM_001318862.1:c.399-185_399-182dup	NP_001305791.1:n.399-185_399-182dup
NM_001318863.1:c.399-185_399-182dup	NP_001305792.1:n.399-185_399-182dup
NR_134893.1:n.416-185_416-182dup
NR_134894.1:n.564-185_564-182dup
NR_134895.1:n.228-185_228-182dup
NR_134896.1:n.398-185_398-182dup
NR_134897.1:n.608-185_608-182dup
NR_134898.1:n.532-185_532-182dup
XM_011532647.2:c.690-185_690-182dup	XP_011530949.1:n.690-185_690-182dup
XM_024452739.1:c.417-185_417-182dup	XP_024308507.1:n.417-185_417-182dup
XR_001738656.1:n.644-185_644-182dup
XR_244926.3:n.675-185_675-182dup
NM_080916.3:c.708-185_708-182dup MANE Select	NP_550438.1:n.708-185_708-182dup
NM_001318859.2:c.426-185_426-182dup	NP_001305788.1:n.426-185_426-182dup
NM_001318860.2:c.417-185_417-182dup	NP_001305789.1:n.417-185_417-182dup
NM_001318861.2:c.417-185_417-182dup	NP_001305790.1:n.417-185_417-182dup
NM_001318862.2:c.399-185_399-182dup	NP_001305791.1:n.399-185_399-182dup
NM_001318863.2:c.399-185_399-182dup	NP_001305792.1:n.399-185_399-182dup
NM_080918.3:c.444-185_444-182dup	NP_550440.1:n.444-185_444-182dup
NR_134893.2:n.362-185_362-182dup
NR_134894.2:n.510-185_510-182dup
NR_134895.2:n.174-185_174-182dup
NR_134896.2:n.344-185_344-182dup
NR_134897.2:n.554-185_554-182dup
NR_134898.2:n.478-185_478-182dup