Canonical Allele Identifier: CA2628203052

Gene: SPG11

Linked Data

• gnomAD v4: 15-44575149-A-AGTCAGAGTAATGGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575149_44575150insGTCAGAGTAATGGGAG , CM000677.2:g.44575149_44575150insGTCAGAGTAATGGGAG	GRCh38
NC_000015.9:g.44867347_44867348insGTCAGAGTAATGGGAG , CM000677.1:g.44867347_44867348insGTCAGAGTAATGGGAG	GRCh37
NC_000015.8:g.42654639_42654640insGTCAGAGTAATGGGAG	NCBI36
NG_008885.1:g.93529_93530insCTCCCATTACTCTGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4492_5867-4491insCTCCCATTACTCTGAC	ENSP00000453246.2:n.5867-4492_5867-4491insCTCCCATTACTCTGAC
ENST00000561391.2:n.2095-109_2095-108insCTCCCATTACTCTGAC
ENST00000682065.1:c.5723-109_5723-108insCTCCCATTACTCTGAC	ENSP00000507025.1:n.5723-109_5723-108insCTCCCATTACTCTGAC
ENST00000682460.1:c.*2124-109_*2124-108insCTCCCATTACTCTGAC	ENSP00000508334.1:n.*2124-109_*2124-108insCTCCCATTACTCTGAC
ENST00000682495.1:c.*2359-109_*2359-108insCTCCCATTACTCTGAC	ENSP00000507166.1:n.*2359-109_*2359-108insCTCCCATTACTCTGAC
ENST00000682669.1:c.5666-109_5666-108insCTCCCATTACTCTGAC	ENSP00000507782.1:n.5666-109_5666-108insCTCCCATTACTCTGAC
ENST00000683186.1:c.*2630-109_*2630-108insCTCCCATTACTCTGAC	ENSP00000507268.1:n.*2630-109_*2630-108insCTCCCATTACTCTGAC
ENST00000683496.1:c.5867-109_5867-108insCTCCCATTACTCTGAC	ENSP00000506968.1:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000683734.1:c.5867-1405_5867-1404insCTCCCATTACTCTGAC	ENSP00000508319.1:n.5867-1405_5867-1404insCTCCCATTACTCTGAC
ENST00000683753.1:n.4913-109_4913-108insCTCCCATTACTCTGAC
ENST00000684038.1:c.*2287-109_*2287-108insCTCCCATTACTCTGAC	ENSP00000507141.1:n.*2287-109_*2287-108insCTCCCATTACTCTGAC
ENST00000684235.1:c.5867-109_5867-108insCTCCCATTACTCTGAC	ENSP00000508295.1:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000684676.1:c.*16-109_*16-108insCTCCCATTACTCTGAC	ENSP00000506948.1:n.*16-109_*16-108insCTCCCATTACTCTGAC
ENST00000261866.12:c.5867-109_5867-108insCTCCCATTACTCTGAC MANE Select	ENSP00000261866.7:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000261866.11:c.5867-109_5867-108insCTCCCATTACTCTGAC	ENSP00000261866.7:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000427534.6:c.5867-109_5867-108insCTCCCATTACTCTGAC	ENSP00000396110.2:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000535302.6:c.5867-2330_5867-2329insCTCCCATTACTCTGAC	ENSP00000445278.2:n.5867-2330_5867-2329insCTCCCATTACTCTGAC
ENST00000558080.1:n.123_124insCTCCCATTACTCTGAC
ENST00000558319.5:c.5867-109_5867-108insCTCCCATTACTCTGAC	ENSP00000453599.1:n.5867-109_5867-108insCTCCCATTACTCTGAC
ENST00000559511.5:c.715-4492_715-4491insCTCCCATTACTCTGAC
ENST00000559822.1:c.410-109_410-108insCTCCCATTACTCTGAC
NM_001160227.1:c.5867-2330_5867-2329insCTCCCATTACTCTGAC	NP_001153699.1:n.5867-2330_5867-2329insCTCCCATTACTCTGAC
NM_025137.3:c.5867-109_5867-108insCTCCCATTACTCTGAC	NP_079413.3:n.5867-109_5867-108insCTCCCATTACTCTGAC
XM_005254695.3:c.5609-109_5609-108insCTCCCATTACTCTGAC	XP_005254752.1:n.5609-109_5609-108insCTCCCATTACTCTGAC
XM_006720700.1:c.5723-109_5723-108insCTCCCATTACTCTGAC	XP_006720763.1:n.5723-109_5723-108insCTCCCATTACTCTGAC
XM_017022634.1:c.5867-109_5867-108insCTCCCATTACTCTGAC	XP_016878123.1:n.5867-109_5867-108insCTCCCATTACTCTGAC
XM_017022636.1:c.2744-109_2744-108insCTCCCATTACTCTGAC	XP_016878125.1:n.2744-109_2744-108insCTCCCATTACTCTGAC
NM_025137.4:c.5867-109_5867-108insCTCCCATTACTCTGAC MANE Select	NP_079413.3:n.5867-109_5867-108insCTCCCATTACTCTGAC
NM_001160227.2:c.5867-2330_5867-2329insCTCCCATTACTCTGAC	NP_001153699.1:n.5867-2330_5867-2329insCTCCCATTACTCTGAC