Canonical Allele Identifier: CA1261201263

Gene: DGUOK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73957965_73957969delinsCCTTT , CM000664.2:g.73957965_73957969delinsCCTTT	GRCh38
NC_000002.11:g.74185092_74185096delinsCCTTT , CM000664.1:g.74185092_74185096delinsCCTTT	GRCh37
NC_000002.10:g.74038600_74038604delinsCCTTT	NCBI36
NG_008044.1:g.36140_36144delinsCCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.708-181_708-177delinsCCTTT MANE Select	ENSP00000264093.4:n.708-181_708-177delinsCCTTT
ENST00000264093.8:c.708-181_708-177delinsCCTTT	ENSP00000264093.4:n.708-181_708-177delinsCCTTT
ENST00000348222.3:c.444-181_444-177delinsCCTTT	ENSP00000306964.3:n.444-181_444-177delinsCCTTT
ENST00000418996.5:c.*61-181_*61-177delinsCCTTT	ENSP00000408209.1:n.*61-181_*61-177delinsCCTTT
ENST00000462685.1:n.537-181_537-177delinsCCTTT
ENST00000489796.5:n.593-181_593-177delinsCCTTT
ENST00000629438.2:c.*325-181_*325-177delinsCCTTT	ENSP00000487122.1:n.*325-181_*325-177delinsCCTTT
NM_080916.2:c.708-181_708-177delinsCCTTT	NP_550438.1:n.708-181_708-177delinsCCTTT
NM_080918.2:c.444-181_444-177delinsCCTTT	NP_550440.1:n.444-181_444-177delinsCCTTT
XM_005264173.2:c.417-181_417-177delinsCCTTT	XP_005264230.1:n.417-181_417-177delinsCCTTT
XM_005264174.1:c.417-181_417-177delinsCCTTT	XP_005264231.1:n.417-181_417-177delinsCCTTT
XM_011532647.1:c.690-181_690-177delinsCCTTT	XP_011530949.1:n.690-181_690-177delinsCCTTT
XM_011532648.1:c.399-181_399-177delinsCCTTT	XP_011530950.1:n.399-181_399-177delinsCCTTT
XR_244926.2:n.673-181_673-177delinsCCTTT
NM_001318859.1:c.426-181_426-177delinsCCTTT	NP_001305788.1:n.426-181_426-177delinsCCTTT
NM_001318860.1:c.417-181_417-177delinsCCTTT	NP_001305789.1:n.417-181_417-177delinsCCTTT
NM_001318861.1:c.417-181_417-177delinsCCTTT	NP_001305790.1:n.417-181_417-177delinsCCTTT
NM_001318862.1:c.399-181_399-177delinsCCTTT	NP_001305791.1:n.399-181_399-177delinsCCTTT
NM_001318863.1:c.399-181_399-177delinsCCTTT	NP_001305792.1:n.399-181_399-177delinsCCTTT
NR_134893.1:n.416-181_416-177delinsCCTTT
NR_134894.1:n.564-181_564-177delinsCCTTT
NR_134895.1:n.228-181_228-177delinsCCTTT
NR_134896.1:n.398-181_398-177delinsCCTTT
NR_134897.1:n.608-181_608-177delinsCCTTT
NR_134898.1:n.532-181_532-177delinsCCTTT
XM_011532647.2:c.690-181_690-177delinsCCTTT	XP_011530949.1:n.690-181_690-177delinsCCTTT
XM_024452739.1:c.417-181_417-177delinsCCTTT	XP_024308507.1:n.417-181_417-177delinsCCTTT
XR_001738656.1:n.644-181_644-177delinsCCTTT
XR_244926.3:n.675-181_675-177delinsCCTTT
NM_080916.3:c.708-181_708-177delinsCCTTT MANE Select	NP_550438.1:n.708-181_708-177delinsCCTTT
NM_001318859.2:c.426-181_426-177delinsCCTTT	NP_001305788.1:n.426-181_426-177delinsCCTTT
NM_001318860.2:c.417-181_417-177delinsCCTTT	NP_001305789.1:n.417-181_417-177delinsCCTTT
NM_001318861.2:c.417-181_417-177delinsCCTTT	NP_001305790.1:n.417-181_417-177delinsCCTTT
NM_001318862.2:c.399-181_399-177delinsCCTTT	NP_001305791.1:n.399-181_399-177delinsCCTTT
NM_001318863.2:c.399-181_399-177delinsCCTTT	NP_001305792.1:n.399-181_399-177delinsCCTTT
NM_080918.3:c.444-181_444-177delinsCCTTT	NP_550440.1:n.444-181_444-177delinsCCTTT
NR_134893.2:n.362-181_362-177delinsCCTTT
NR_134894.2:n.510-181_510-177delinsCCTTT
NR_134895.2:n.174-181_174-177delinsCCTTT
NR_134896.2:n.344-181_344-177delinsCCTTT
NR_134897.2:n.554-181_554-177delinsCCTTT
NR_134898.2:n.478-181_478-177delinsCCTTT