Canonical Allele Identifier: CA1261201246

Gene: DGUOK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73957923_73957927delinsCTGTT , CM000664.2:g.73957923_73957927delinsCTGTT	GRCh38
NC_000002.11:g.74185050_74185054delinsCTGTT , CM000664.1:g.74185050_74185054delinsCTGTT	GRCh37
NC_000002.10:g.74038558_74038562delinsCTGTT	NCBI36
NG_008044.1:g.36098_36102delinsCTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.708-223_708-219delinsCTGTT MANE Select	ENSP00000264093.4:n.708-223_708-219delinsCTGTT
ENST00000264093.8:c.708-223_708-219delinsCTGTT	ENSP00000264093.4:n.708-223_708-219delinsCTGTT
ENST00000348222.3:c.444-223_444-219delinsCTGTT	ENSP00000306964.3:n.444-223_444-219delinsCTGTT
ENST00000418996.5:c.*61-223_*61-219delinsCTGTT	ENSP00000408209.1:n.*61-223_*61-219delinsCTGTT
ENST00000462685.1:n.537-223_537-219delinsCTGTT
ENST00000489796.5:n.593-223_593-219delinsCTGTT
ENST00000629438.2:c.*325-223_*325-219delinsCTGTT	ENSP00000487122.1:n.*325-223_*325-219delinsCTGTT
NM_080916.2:c.708-223_708-219delinsCTGTT	NP_550438.1:n.708-223_708-219delinsCTGTT
NM_080918.2:c.444-223_444-219delinsCTGTT	NP_550440.1:n.444-223_444-219delinsCTGTT
XM_005264173.2:c.417-223_417-219delinsCTGTT	XP_005264230.1:n.417-223_417-219delinsCTGTT
XM_005264174.1:c.417-223_417-219delinsCTGTT	XP_005264231.1:n.417-223_417-219delinsCTGTT
XM_011532647.1:c.690-223_690-219delinsCTGTT	XP_011530949.1:n.690-223_690-219delinsCTGTT
XM_011532648.1:c.399-223_399-219delinsCTGTT	XP_011530950.1:n.399-223_399-219delinsCTGTT
XR_244926.2:n.673-223_673-219delinsCTGTT
NM_001318859.1:c.426-223_426-219delinsCTGTT	NP_001305788.1:n.426-223_426-219delinsCTGTT
NM_001318860.1:c.417-223_417-219delinsCTGTT	NP_001305789.1:n.417-223_417-219delinsCTGTT
NM_001318861.1:c.417-223_417-219delinsCTGTT	NP_001305790.1:n.417-223_417-219delinsCTGTT
NM_001318862.1:c.399-223_399-219delinsCTGTT	NP_001305791.1:n.399-223_399-219delinsCTGTT
NM_001318863.1:c.399-223_399-219delinsCTGTT	NP_001305792.1:n.399-223_399-219delinsCTGTT
NR_134893.1:n.416-223_416-219delinsCTGTT
NR_134894.1:n.564-223_564-219delinsCTGTT
NR_134895.1:n.228-223_228-219delinsCTGTT
NR_134896.1:n.398-223_398-219delinsCTGTT
NR_134897.1:n.608-223_608-219delinsCTGTT
NR_134898.1:n.532-223_532-219delinsCTGTT
XM_011532647.2:c.690-223_690-219delinsCTGTT	XP_011530949.1:n.690-223_690-219delinsCTGTT
XM_024452739.1:c.417-223_417-219delinsCTGTT	XP_024308507.1:n.417-223_417-219delinsCTGTT
XR_001738656.1:n.644-223_644-219delinsCTGTT
XR_244926.3:n.675-223_675-219delinsCTGTT
NM_080916.3:c.708-223_708-219delinsCTGTT MANE Select	NP_550438.1:n.708-223_708-219delinsCTGTT
NM_001318859.2:c.426-223_426-219delinsCTGTT	NP_001305788.1:n.426-223_426-219delinsCTGTT
NM_001318860.2:c.417-223_417-219delinsCTGTT	NP_001305789.1:n.417-223_417-219delinsCTGTT
NM_001318861.2:c.417-223_417-219delinsCTGTT	NP_001305790.1:n.417-223_417-219delinsCTGTT
NM_001318862.2:c.399-223_399-219delinsCTGTT	NP_001305791.1:n.399-223_399-219delinsCTGTT
NM_001318863.2:c.399-223_399-219delinsCTGTT	NP_001305792.1:n.399-223_399-219delinsCTGTT
NM_080918.3:c.444-223_444-219delinsCTGTT	NP_550440.1:n.444-223_444-219delinsCTGTT
NR_134893.2:n.362-223_362-219delinsCTGTT
NR_134894.2:n.510-223_510-219delinsCTGTT
NR_134895.2:n.174-223_174-219delinsCTGTT
NR_134896.2:n.344-223_344-219delinsCTGTT
NR_134897.2:n.554-223_554-219delinsCTGTT
NR_134898.2:n.478-223_478-219delinsCTGTT