Canonical Allele Identifier: CA344357
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 41326
ClinVar RCV Id: RCV000034227
dbSNP Id: rs312262769

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44583980del , CM000677.2:g.44583980del GRCh38
NC_000015.9:g.44876178del , CM000677.1:g.44876178del GRCh37
NC_000015.8:g.42663470del NCBI36
NG_008885.1:g.84702del

Transcript Alleles

HGVS Amino-acid change
ENST00000559511.6:c.5703del ENSP00000453246.2:p.His1902IlefsTer?
ENST00000561391.2:n.1931del
ENST00000682065.1:c.5559del ENSP00000507025.1:p.His1854IlefsTer?
ENST00000682460.1:c.*1960del ENSP00000508334.1:n.*1960del
ENST00000682495.1:c.*2195del ENSP00000507166.1:n.*2195del
ENST00000682669.1:c.5502del ENSP00000507782.1:p.His1835IlefsTer?
ENST00000683186.1:c.*2466del ENSP00000507268.1:n.*2466del
ENST00000683496.1:c.5703del ENSP00000506968.1:p.His1902IlefsTer?
ENST00000683734.1:c.5703del ENSP00000508319.1:p.His1902IlefsTer?
ENST00000683753.1:n.4749del
ENST00000684038.1:c.*2123del ENSP00000507141.1:n.*2123del
ENST00000684235.1:c.5703del ENSP00000508295.1:p.His1902IlefsTer?
ENST00000684676.1:c.5516-42del ENSP00000506948.1:n.5516-42del
ENST00000261866.12:c.5703del MANE Select ENSP00000261866.7:p.His1902IlefsTer?
ENST00000261866.11:c.5703del ENSP00000261866.7:p.His1902IlefsTer?
ENST00000427534.6:c.5703del ENSP00000396110.2:p.His1902IlefsTer?
ENST00000535302.6:c.5703del ENSP00000445278.2:p.His1902IlefsTer?
ENST00000558319.5:c.5703del ENSP00000453599.1:p.His1902IlefsTer?
ENST00000559511.5:c.551del
ENST00000559822.1:c.288-42del
NM_001160227.1:c.5703del NP_001153699.1:p.His1902IlefsTer?
NM_025137.3:c.5703del NP_079413.3:p.His1902IlefsTer?
XM_005254695.3:c.5445del XP_005254752.1:p.His1816IlefsTer?
XM_006720700.1:c.5559del XP_006720763.1:p.His1854IlefsTer?
XM_017022634.1:c.5703del XP_016878123.1:p.His1902IlefsTer?
XM_017022636.1:c.2580del XP_016878125.1:p.His861IlefsTer?
NM_025137.4:c.5703del MANE Select NP_079413.3:p.His1902IlefsTer?
NM_001160227.2:c.5703del NP_001153699.1:p.His1902IlefsTer?