Canonical Allele Identifier: CA2173685999

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584253G= , CM000677.2:g.44584253G=	GRCh38
NC_000015.9:g.44876451G= , CM000677.1:g.44876451G=	GRCh37
NC_000015.8:g.42663743G=	NCBI36
NG_008885.1:g.84426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5427C=	ENSP00000453246.2:p.His1809=
ENST00000561391.2:n.1655C=
ENST00000682065.1:c.5283C=	ENSP00000507025.1:p.His1761=
ENST00000682460.1:c.*1684C=	ENSP00000508334.1:n.*1684C=
ENST00000682495.1:c.*1919C=	ENSP00000507166.1:n.*1919C=
ENST00000682669.1:c.5226C=	ENSP00000507782.1:p.His1742=
ENST00000683186.1:c.*2190C=	ENSP00000507268.1:n.*2190C=
ENST00000683496.1:c.5427C=	ENSP00000506968.1:p.His1809=
ENST00000683734.1:c.5427C=	ENSP00000508319.1:p.His1809=
ENST00000683753.1:n.4473C=
ENST00000684038.1:c.*1847C=	ENSP00000507141.1:n.*1847C=
ENST00000684235.1:c.5427C=	ENSP00000508295.1:p.His1809=
ENST00000684676.1:c.5427C=	ENSP00000506948.1:p.His1809=
ENST00000261866.12:c.5427C= MANE Select	ENSP00000261866.7:p.His1809=
ENST00000261866.11:c.5427C=	ENSP00000261866.7:p.His1809=
ENST00000427534.6:c.5427C=	ENSP00000396110.2:p.His1809=
ENST00000535302.6:c.5427C=	ENSP00000445278.2:p.His1809=
ENST00000558319.5:c.5427C=	ENSP00000453599.1:p.His1809=
ENST00000559511.5:c.275C=
ENST00000559822.1:c.199C=
NM_001160227.1:c.5427C=	NP_001153699.1:p.His1809=
NM_025137.3:c.5427C=	NP_079413.3:p.His1809=
XM_005254695.3:c.5169C=	XP_005254752.1:p.His1723=
XM_006720700.1:c.5283C=	XP_006720763.1:p.His1761=
XM_017022634.1:c.5427C=	XP_016878123.1:p.His1809=
XM_017022636.1:c.2304C=	XP_016878125.1:p.His768=
NM_025137.4:c.5427C= MANE Select	NP_079413.3:p.His1809=
NM_001160227.2:c.5427C=	NP_001153699.1:p.His1809=