Canonical Allele Identifier: CA2173690304

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575080A= , CM000677.2:g.44575080A=	GRCh38
NC_000015.9:g.44867278A= , CM000677.1:g.44867278A=	GRCh37
NC_000015.8:g.42654570A=	NCBI36
NG_008885.1:g.93599T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4422T=	ENSP00000453246.2:n.5867-4422T=
ENST00000561391.2:n.2095-39T=
ENST00000682065.1:c.5723-39T=	ENSP00000507025.1:n.5723-39T=
ENST00000682460.1:c.*2124-39T=	ENSP00000508334.1:n.*2124-39T=
ENST00000682495.1:c.*2359-39T=	ENSP00000507166.1:n.*2359-39T=
ENST00000682669.1:c.5666-39T=	ENSP00000507782.1:n.5666-39T=
ENST00000683186.1:c.*2630-39T=	ENSP00000507268.1:n.*2630-39T=
ENST00000683496.1:c.5867-39T=	ENSP00000506968.1:n.5867-39T=
ENST00000683734.1:c.5867-1335T=	ENSP00000508319.1:n.5867-1335T=
ENST00000683753.1:n.4913-39T=
ENST00000684038.1:c.*2287-39T=	ENSP00000507141.1:n.*2287-39T=
ENST00000684235.1:c.5867-39T=	ENSP00000508295.1:n.5867-39T=
ENST00000684676.1:c.*16-39T=	ENSP00000506948.1:n.*16-39T=
ENST00000261866.12:c.5867-39T= MANE Select	ENSP00000261866.7:n.5867-39T=
ENST00000261866.11:c.5867-39T=	ENSP00000261866.7:n.5867-39T=
ENST00000427534.6:c.5867-39T=	ENSP00000396110.2:n.5867-39T=
ENST00000535302.6:c.5867-2260T=	ENSP00000445278.2:n.5867-2260T=
ENST00000558080.1:n.193T=
ENST00000558319.5:c.5867-39T=	ENSP00000453599.1:n.5867-39T=
ENST00000559511.5:c.715-4422T=
ENST00000559822.1:c.410-39T=
NM_001160227.1:c.5867-2260T=	NP_001153699.1:n.5867-2260T=
NM_025137.3:c.5867-39T=	NP_079413.3:n.5867-39T=
XM_005254695.3:c.5609-39T=	XP_005254752.1:n.5609-39T=
XM_006720700.1:c.5723-39T=	XP_006720763.1:n.5723-39T=
XM_017022634.1:c.5867-39T=	XP_016878123.1:n.5867-39T=
XM_017022636.1:c.2744-39T=	XP_016878125.1:n.2744-39T=
NM_025137.4:c.5867-39T= MANE Select	NP_079413.3:n.5867-39T=
NM_001160227.2:c.5867-2260T=	NP_001153699.1:n.5867-2260T=