Canonical Allele Identifier: CA336745
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 216127
ClinVar RCV Id: RCV000196838
dbSNP Id: rs863224524

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44622336del , CM000677.2:g.44622336del GRCh38
NC_000015.9:g.44914534del , CM000677.1:g.44914534del GRCh37
NC_000015.8:g.42701826del NCBI36
NG_008885.1:g.46346del

Transcript Alleles

HGVS Amino-acid change
ENST00000559511.6:c.2331del ENSP00000453246.2:p.Glu778LysfsTer13
ENST00000682065.1:c.2331del ENSP00000507025.1:p.Glu778LysfsTer13
ENST00000682460.1:c.2331del ENSP00000508334.1:p.Glu778LysfsTer13
ENST00000682495.1:c.2331del ENSP00000507166.1:p.Glu778LysfsTer13
ENST00000682669.1:c.2331del ENSP00000507782.1:p.Glu778LysfsTer13
ENST00000682788.1:c.2331del ENSP00000508089.1:p.Glu778LysfsTer13
ENST00000682877.1:n.2742del
ENST00000682915.1:c.2331del ENSP00000507493.1:p.Glu778LysfsTer13
ENST00000683121.1:c.2331del ENSP00000507557.1:p.Glu778LysfsTer13
ENST00000683186.1:c.2331del ENSP00000507268.1:p.Glu778LysfsTer13
ENST00000683255.1:c.2331del ENSP00000508340.1:p.Glu778LysfsTer13
ENST00000683496.1:c.2331del ENSP00000506968.1:p.Glu778LysfsTer13
ENST00000683573.1:c.2331del ENSP00000508031.1:p.Glu778LysfsTer13
ENST00000683734.1:c.2331del ENSP00000508319.1:p.Glu778LysfsTer13
ENST00000683753.1:n.1455del
ENST00000684038.1:c.2073del ENSP00000507141.1:p.Glu692LysfsTer13
ENST00000684235.1:c.2331del ENSP00000508295.1:p.Glu778LysfsTer13
ENST00000684676.1:c.2331del ENSP00000506948.1:p.Glu778LysfsTer13
ENST00000261866.12:c.2331del MANE Select ENSP00000261866.7:p.Glu778LysfsTer13
ENST00000261866.11:c.2331del ENSP00000261866.7:p.Glu778LysfsTer13
ENST00000427534.6:c.2331del ENSP00000396110.2:p.Glu778LysfsTer13
ENST00000535302.6:c.2331del ENSP00000445278.2:p.Glu778LysfsTer13
ENST00000558319.5:c.2331del ENSP00000453599.1:p.Glu778LysfsTer13
NM_001160227.1:c.2331del NP_001153699.1:p.Glu778LysfsTer13
NM_025137.3:c.2331del NP_079413.3:p.Glu778LysfsTer13
XM_005254695.3:c.2073del XP_005254752.1:p.Glu692LysfsTer13
XM_006720700.1:c.2331del XP_006720763.1:p.Glu778LysfsTer13
XM_006720701.2:c.2331del XP_006720764.1:p.Glu778LysfsTer13
XM_011522093.1:c.2331del XP_011520395.1:p.Glu778LysfsTer13
XR_931917.1:n.2362del
XM_006720701.3:c.2331del XP_006720764.1:p.Glu778LysfsTer13
XM_017022634.1:c.2331del XP_016878123.1:p.Glu778LysfsTer13
XM_017022635.2:c.2331del XP_016878124.1:p.Glu778LysfsTer13
XM_017022636.1:c.-686del XP_016878125.1:n.-686del
XR_001751402.1:n.2362del
XR_931917.2:n.2362del
NM_025137.4:c.2331del MANE Select NP_079413.3:p.Glu778LysfsTer13
NM_001160227.2:c.2331del NP_001153699.1:p.Glu778LysfsTer13