Canonical Allele Identifier: CA2173686166

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584282G= , CM000677.2:g.44584282G=	GRCh38
NC_000015.9:g.44876480G= , CM000677.1:g.44876480G=	GRCh37
NC_000015.8:g.42663772G=	NCBI36
NG_008885.1:g.84397C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5398C=	ENSP00000453246.2:p.Gln1800=
ENST00000561391.2:n.1626C=
ENST00000682065.1:c.5254C=	ENSP00000507025.1:p.Gln1752=
ENST00000682460.1:c.*1655C=	ENSP00000508334.1:n.*1655C=
ENST00000682495.1:c.*1890C=	ENSP00000507166.1:n.*1890C=
ENST00000682669.1:c.5197C=	ENSP00000507782.1:p.Gln1733=
ENST00000683186.1:c.*2161C=	ENSP00000507268.1:n.*2161C=
ENST00000683496.1:c.5398C=	ENSP00000506968.1:p.Gln1800=
ENST00000683734.1:c.5398C=	ENSP00000508319.1:p.Gln1800=
ENST00000683753.1:n.4444C=
ENST00000684038.1:c.*1818C=	ENSP00000507141.1:n.*1818C=
ENST00000684235.1:c.5398C=	ENSP00000508295.1:p.Gln1800=
ENST00000684676.1:c.5398C=	ENSP00000506948.1:p.Gln1800=
ENST00000261866.12:c.5398C= MANE Select	ENSP00000261866.7:p.Gln1800=
ENST00000261866.11:c.5398C=	ENSP00000261866.7:p.Gln1800=
ENST00000427534.6:c.5398C=	ENSP00000396110.2:p.Gln1800=
ENST00000535302.6:c.5398C=	ENSP00000445278.2:p.Gln1800=
ENST00000558319.5:c.5398C=	ENSP00000453599.1:p.Gln1800=
ENST00000558790.5:n.835C=
ENST00000559511.5:c.246C=
ENST00000559822.1:c.170C=
NM_001160227.1:c.5398C=	NP_001153699.1:p.Gln1800=
NM_025137.3:c.5398C=	NP_079413.3:p.Gln1800=
XM_005254695.3:c.5140C=	XP_005254752.1:p.Gln1714=
XM_006720700.1:c.5254C=	XP_006720763.1:p.Gln1752=
XM_017022634.1:c.5398C=	XP_016878123.1:p.Gln1800=
XM_017022636.1:c.2275C=	XP_016878125.1:p.Gln759=
XR_931917.2:n.5452C=
NM_025137.4:c.5398C= MANE Select	NP_079413.3:p.Gln1800=
NM_001160227.2:c.5398C=	NP_001153699.1:p.Gln1800=