Canonical Allele Identifier: CA2695220744

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584190del , CM000677.2:g.44584190del	GRCh38
NC_000015.9:g.44876388del , CM000677.1:g.44876388del	GRCh37
NC_000015.8:g.42663680del	NCBI36
NG_008885.1:g.84489del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5490del	ENSP00000453246.2:p.Glu1831AsnfsTer7
ENST00000561391.2:n.1718del
ENST00000682065.1:c.5346del	ENSP00000507025.1:p.Glu1783AsnfsTer7
ENST00000682460.1:c.*1747del	ENSP00000508334.1:n.*1747del
ENST00000682495.1:c.*1982del	ENSP00000507166.1:n.*1982del
ENST00000682669.1:c.5289del	ENSP00000507782.1:p.Glu1764AsnfsTer7
ENST00000683186.1:c.*2253del	ENSP00000507268.1:n.*2253del
ENST00000683496.1:c.5490del	ENSP00000506968.1:p.Glu1831AsnfsTer7
ENST00000683734.1:c.5490del	ENSP00000508319.1:p.Glu1831AsnfsTer7
ENST00000683753.1:n.4536del
ENST00000684038.1:c.*1910del	ENSP00000507141.1:n.*1910del
ENST00000684235.1:c.5490del	ENSP00000508295.1:p.Glu1831AsnfsTer7
ENST00000684676.1:c.5490del	ENSP00000506948.1:p.Glu1831AsnfsTer7
ENST00000261866.12:c.5490del MANE Select	ENSP00000261866.7:p.Glu1831AsnfsTer7
ENST00000261866.11:c.5490del	ENSP00000261866.7:p.Glu1831AsnfsTer7
ENST00000427534.6:c.5490del	ENSP00000396110.2:p.Glu1831AsnfsTer7
ENST00000535302.6:c.5490del	ENSP00000445278.2:p.Glu1831AsnfsTer7
ENST00000558319.5:c.5490del	ENSP00000453599.1:p.Glu1831AsnfsTer7
ENST00000559511.5:c.338del
ENST00000559822.1:c.262del
NM_001160227.1:c.5490del	NP_001153699.1:p.Glu1831AsnfsTer7
NM_025137.3:c.5490del	NP_079413.3:p.Glu1831AsnfsTer7
XM_005254695.3:c.5232del	XP_005254752.1:p.Glu1745AsnfsTer7
XM_006720700.1:c.5346del	XP_006720763.1:p.Glu1783AsnfsTer7
XM_017022634.1:c.5490del	XP_016878123.1:p.Glu1831AsnfsTer7
XM_017022636.1:c.2367del	XP_016878125.1:p.Glu790AsnfsTer7
NM_025137.4:c.5490del MANE Select	NP_079413.3:p.Glu1831AsnfsTer7
NM_001160227.2:c.5490del	NP_001153699.1:p.Glu1831AsnfsTer7