Canonical Allele Identifier: CA1261201264

Gene: DGUOK

Linked Data

• dbSNP Id: rs1683247922

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73957968_73957971del , CM000664.2:g.73957968_73957971del	GRCh38
NC_000002.11:g.74185095_74185098del , CM000664.1:g.74185095_74185098del	GRCh37
NC_000002.10:g.74038603_74038606del	NCBI36
NG_008044.1:g.36143_36146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.708-178_708-175del MANE Select	ENSP00000264093.4:n.708-178_708-175del
ENST00000264093.8:c.708-178_708-175del	ENSP00000264093.4:n.708-178_708-175del
ENST00000348222.3:c.444-178_444-175del	ENSP00000306964.3:n.444-178_444-175del
ENST00000418996.5:c.*61-178_*61-175del	ENSP00000408209.1:n.*61-178_*61-175del
ENST00000462685.1:n.537-178_537-175del
ENST00000489796.5:n.593-178_593-175del
ENST00000629438.2:c.*325-178_*325-175del	ENSP00000487122.1:n.*325-178_*325-175del
NM_080916.2:c.708-178_708-175del	NP_550438.1:n.708-178_708-175del
NM_080918.2:c.444-178_444-175del	NP_550440.1:n.444-178_444-175del
XM_005264173.2:c.417-178_417-175del	XP_005264230.1:n.417-178_417-175del
XM_005264174.1:c.417-178_417-175del	XP_005264231.1:n.417-178_417-175del
XM_011532647.1:c.690-178_690-175del	XP_011530949.1:n.690-178_690-175del
XM_011532648.1:c.399-178_399-175del	XP_011530950.1:n.399-178_399-175del
XR_244926.2:n.673-178_673-175del
NM_001318859.1:c.426-178_426-175del	NP_001305788.1:n.426-178_426-175del
NM_001318860.1:c.417-178_417-175del	NP_001305789.1:n.417-178_417-175del
NM_001318861.1:c.417-178_417-175del	NP_001305790.1:n.417-178_417-175del
NM_001318862.1:c.399-178_399-175del	NP_001305791.1:n.399-178_399-175del
NM_001318863.1:c.399-178_399-175del	NP_001305792.1:n.399-178_399-175del
NR_134893.1:n.416-178_416-175del
NR_134894.1:n.564-178_564-175del
NR_134895.1:n.228-178_228-175del
NR_134896.1:n.398-178_398-175del
NR_134897.1:n.608-178_608-175del
NR_134898.1:n.532-178_532-175del
XM_011532647.2:c.690-178_690-175del	XP_011530949.1:n.690-178_690-175del
XM_024452739.1:c.417-178_417-175del	XP_024308507.1:n.417-178_417-175del
XR_001738656.1:n.644-178_644-175del
XR_244926.3:n.675-178_675-175del
NM_080916.3:c.708-178_708-175del MANE Select	NP_550438.1:n.708-178_708-175del
NM_001318859.2:c.426-178_426-175del	NP_001305788.1:n.426-178_426-175del
NM_001318860.2:c.417-178_417-175del	NP_001305789.1:n.417-178_417-175del
NM_001318861.2:c.417-178_417-175del	NP_001305790.1:n.417-178_417-175del
NM_001318862.2:c.399-178_399-175del	NP_001305791.1:n.399-178_399-175del
NM_001318863.2:c.399-178_399-175del	NP_001305792.1:n.399-178_399-175del
NM_080918.3:c.444-178_444-175del	NP_550440.1:n.444-178_444-175del
NR_134893.2:n.362-178_362-175del
NR_134894.2:n.510-178_510-175del
NR_134895.2:n.174-178_174-175del
NR_134896.2:n.344-178_344-175del
NR_134897.2:n.554-178_554-175del
NR_134898.2:n.478-178_478-175del