Canonical Allele Identifier: CA892905553
Gene: DGUOK HGNC NCBI

Linked Data

dbSNP Id: rs774856089

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73957928_73957931dup , CM000664.2:g.73957928_73957931dup GRCh38
NC_000002.11:g.74185055_74185058dup , CM000664.1:g.74185055_74185058dup GRCh37
NC_000002.10:g.74038563_74038566dup NCBI36
NG_008044.1:g.36103_36106dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264093.9:c.708-218_708-215dup MANE Select ENSP00000264093.4:n.708-218_708-215dup
ENST00000264093.8:c.708-218_708-215dup ENSP00000264093.4:n.708-218_708-215dup
ENST00000348222.3:c.444-218_444-215dup ENSP00000306964.3:n.444-218_444-215dup
ENST00000418996.5:c.*61-218_*61-215dup ENSP00000408209.1:n.*61-218_*61-215dup
ENST00000462685.1:n.537-218_537-215dup
ENST00000489796.5:n.593-218_593-215dup
ENST00000629438.2:c.*325-218_*325-215dup ENSP00000487122.1:n.*325-218_*325-215dup
NM_080916.2:c.708-218_708-215dup NP_550438.1:n.708-218_708-215dup
NM_080918.2:c.444-218_444-215dup NP_550440.1:n.444-218_444-215dup
XM_005264173.2:c.417-218_417-215dup XP_005264230.1:n.417-218_417-215dup
XM_005264174.1:c.417-218_417-215dup XP_005264231.1:n.417-218_417-215dup
XM_011532647.1:c.690-218_690-215dup XP_011530949.1:n.690-218_690-215dup
XM_011532648.1:c.399-218_399-215dup XP_011530950.1:n.399-218_399-215dup
XR_244926.2:n.673-218_673-215dup
NM_001318859.1:c.426-218_426-215dup NP_001305788.1:n.426-218_426-215dup
NM_001318860.1:c.417-218_417-215dup NP_001305789.1:n.417-218_417-215dup
NM_001318861.1:c.417-218_417-215dup NP_001305790.1:n.417-218_417-215dup
NM_001318862.1:c.399-218_399-215dup NP_001305791.1:n.399-218_399-215dup
NM_001318863.1:c.399-218_399-215dup NP_001305792.1:n.399-218_399-215dup
NR_134893.1:n.416-218_416-215dup
NR_134894.1:n.564-218_564-215dup
NR_134895.1:n.228-218_228-215dup
NR_134896.1:n.398-218_398-215dup
NR_134897.1:n.608-218_608-215dup
NR_134898.1:n.532-218_532-215dup
XM_011532647.2:c.690-218_690-215dup XP_011530949.1:n.690-218_690-215dup
XM_024452739.1:c.417-218_417-215dup XP_024308507.1:n.417-218_417-215dup
XR_001738656.1:n.644-218_644-215dup
XR_244926.3:n.675-218_675-215dup
NM_080916.3:c.708-218_708-215dup MANE Select NP_550438.1:n.708-218_708-215dup
NM_001318859.2:c.426-218_426-215dup NP_001305788.1:n.426-218_426-215dup
NM_001318860.2:c.417-218_417-215dup NP_001305789.1:n.417-218_417-215dup
NM_001318861.2:c.417-218_417-215dup NP_001305790.1:n.417-218_417-215dup
NM_001318862.2:c.399-218_399-215dup NP_001305791.1:n.399-218_399-215dup
NM_001318863.2:c.399-218_399-215dup NP_001305792.1:n.399-218_399-215dup
NM_080918.3:c.444-218_444-215dup NP_550440.1:n.444-218_444-215dup
NR_134893.2:n.362-218_362-215dup
NR_134894.2:n.510-218_510-215dup
NR_134895.2:n.174-218_174-215dup
NR_134896.2:n.344-218_344-215dup
NR_134897.2:n.554-218_554-215dup
NR_134898.2:n.478-218_478-215dup