Canonical Allele Identifier: CA1261201244

Gene: DGUOK

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73957918_73957922delinsTCTGA , CM000664.2:g.73957918_73957922delinsTCTGA	GRCh38
NC_000002.11:g.74185045_74185049delinsTCTGA , CM000664.1:g.74185045_74185049delinsTCTGA	GRCh37
NC_000002.10:g.74038553_74038557delinsTCTGA	NCBI36
NG_008044.1:g.36093_36097delinsTCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264093.9:c.708-228_708-224delinsTCTGA MANE Select	ENSP00000264093.4:n.708-228_708-224delinsTCTGA
ENST00000264093.8:c.708-228_708-224delinsTCTGA	ENSP00000264093.4:n.708-228_708-224delinsTCTGA
ENST00000348222.3:c.444-228_444-224delinsTCTGA	ENSP00000306964.3:n.444-228_444-224delinsTCTGA
ENST00000418996.5:c.*61-228_*61-224delinsTCTGA	ENSP00000408209.1:n.*61-228_*61-224delinsTCTGA
ENST00000462685.1:n.537-228_537-224delinsTCTGA
ENST00000489796.5:n.593-228_593-224delinsTCTGA
ENST00000629438.2:c.*325-228_*325-224delinsTCTGA	ENSP00000487122.1:n.*325-228_*325-224delinsTCTGA
NM_080916.2:c.708-228_708-224delinsTCTGA	NP_550438.1:n.708-228_708-224delinsTCTGA
NM_080918.2:c.444-228_444-224delinsTCTGA	NP_550440.1:n.444-228_444-224delinsTCTGA
XM_005264173.2:c.417-228_417-224delinsTCTGA	XP_005264230.1:n.417-228_417-224delinsTCTGA
XM_005264174.1:c.417-228_417-224delinsTCTGA	XP_005264231.1:n.417-228_417-224delinsTCTGA
XM_011532647.1:c.690-228_690-224delinsTCTGA	XP_011530949.1:n.690-228_690-224delinsTCTGA
XM_011532648.1:c.399-228_399-224delinsTCTGA	XP_011530950.1:n.399-228_399-224delinsTCTGA
XR_244926.2:n.673-228_673-224delinsTCTGA
NM_001318859.1:c.426-228_426-224delinsTCTGA	NP_001305788.1:n.426-228_426-224delinsTCTGA
NM_001318860.1:c.417-228_417-224delinsTCTGA	NP_001305789.1:n.417-228_417-224delinsTCTGA
NM_001318861.1:c.417-228_417-224delinsTCTGA	NP_001305790.1:n.417-228_417-224delinsTCTGA
NM_001318862.1:c.399-228_399-224delinsTCTGA	NP_001305791.1:n.399-228_399-224delinsTCTGA
NM_001318863.1:c.399-228_399-224delinsTCTGA	NP_001305792.1:n.399-228_399-224delinsTCTGA
NR_134893.1:n.416-228_416-224delinsTCTGA
NR_134894.1:n.564-228_564-224delinsTCTGA
NR_134895.1:n.228-228_228-224delinsTCTGA
NR_134896.1:n.398-228_398-224delinsTCTGA
NR_134897.1:n.608-228_608-224delinsTCTGA
NR_134898.1:n.532-228_532-224delinsTCTGA
XM_011532647.2:c.690-228_690-224delinsTCTGA	XP_011530949.1:n.690-228_690-224delinsTCTGA
XM_024452739.1:c.417-228_417-224delinsTCTGA	XP_024308507.1:n.417-228_417-224delinsTCTGA
XR_001738656.1:n.644-228_644-224delinsTCTGA
XR_244926.3:n.675-228_675-224delinsTCTGA
NM_080916.3:c.708-228_708-224delinsTCTGA MANE Select	NP_550438.1:n.708-228_708-224delinsTCTGA
NM_001318859.2:c.426-228_426-224delinsTCTGA	NP_001305788.1:n.426-228_426-224delinsTCTGA
NM_001318860.2:c.417-228_417-224delinsTCTGA	NP_001305789.1:n.417-228_417-224delinsTCTGA
NM_001318861.2:c.417-228_417-224delinsTCTGA	NP_001305790.1:n.417-228_417-224delinsTCTGA
NM_001318862.2:c.399-228_399-224delinsTCTGA	NP_001305791.1:n.399-228_399-224delinsTCTGA
NM_001318863.2:c.399-228_399-224delinsTCTGA	NP_001305792.1:n.399-228_399-224delinsTCTGA
NM_080918.3:c.444-228_444-224delinsTCTGA	NP_550440.1:n.444-228_444-224delinsTCTGA
NR_134893.2:n.362-228_362-224delinsTCTGA
NR_134894.2:n.510-228_510-224delinsTCTGA
NR_134895.2:n.174-228_174-224delinsTCTGA
NR_134896.2:n.344-228_344-224delinsTCTGA
NR_134897.2:n.554-228_554-224delinsTCTGA
NR_134898.2:n.478-228_478-224delinsTCTGA