Canonical Allele Identifier: CA713046702

Gene: SPG11

Linked Data

• dbSNP Id: rs1471931750
• MyVariant Identifiers: chr15:g.44952492_44952493insAG (hg19) ; chr15:g.44660294_44660295insAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44660295_44660296insGA , CM000677.2:g.44660295_44660296insGA	GRCh38
NC_000015.9:g.44952493_44952494insGA , CM000677.1:g.44952493_44952494insGA	GRCh37
NC_000015.8:g.42739785_42739786insGA	NCBI36
NG_008885.1:g.8384_8385insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.442+137_442+138insCT	ENSP00000453246.2:n.442+137_442+138insCT
ENST00000682065.1:c.442+137_442+138insCT	ENSP00000507025.1:n.442+137_442+138insCT
ENST00000682410.1:n.471+137_471+138insCT
ENST00000682460.1:c.442+137_442+138insCT	ENSP00000508334.1:n.442+137_442+138insCT
ENST00000682495.1:c.442+137_442+138insCT	ENSP00000507166.1:n.442+137_442+138insCT
ENST00000682648.1:n.387+137_387+138insCT
ENST00000682669.1:c.442+137_442+138insCT	ENSP00000507782.1:n.442+137_442+138insCT
ENST00000682788.1:c.442+137_442+138insCT	ENSP00000508089.1:n.442+137_442+138insCT
ENST00000682877.1:n.473+137_473+138insCT
ENST00000682915.1:c.442+137_442+138insCT	ENSP00000507493.1:n.442+137_442+138insCT
ENST00000683121.1:c.442+137_442+138insCT	ENSP00000507557.1:n.442+137_442+138insCT
ENST00000683186.1:c.442+137_442+138insCT	ENSP00000507268.1:n.442+137_442+138insCT
ENST00000683255.1:c.442+137_442+138insCT	ENSP00000508340.1:n.442+137_442+138insCT
ENST00000683496.1:c.442+137_442+138insCT	ENSP00000506968.1:n.442+137_442+138insCT
ENST00000683573.1:c.442+137_442+138insCT	ENSP00000508031.1:n.442+137_442+138insCT
ENST00000683734.1:c.442+137_442+138insCT	ENSP00000508319.1:n.442+137_442+138insCT
ENST00000684038.1:c.442+137_442+138insCT	ENSP00000507141.1:n.442+137_442+138insCT
ENST00000684235.1:c.442+137_442+138insCT	ENSP00000508295.1:n.442+137_442+138insCT
ENST00000684490.1:n.457+137_457+138insCT
ENST00000684676.1:c.442+137_442+138insCT	ENSP00000506948.1:n.442+137_442+138insCT
ENST00000261866.12:c.442+137_442+138insCT MANE Select	ENSP00000261866.7:n.442+137_442+138insCT
ENST00000261866.11:c.442+137_442+138insCT	ENSP00000261866.7:n.442+137_442+138insCT
ENST00000427534.6:c.442+137_442+138insCT	ENSP00000396110.2:n.442+137_442+138insCT
ENST00000535302.6:c.442+137_442+138insCT	ENSP00000445278.2:n.442+137_442+138insCT
ENST00000558319.5:c.442+137_442+138insCT	ENSP00000453599.1:n.442+137_442+138insCT
ENST00000559193.5:c.442+137_442+138insCT	ENSP00000453848.1:n.442+137_442+138insCT
NM_001160227.1:c.442+137_442+138insCT	NP_001153699.1:n.442+137_442+138insCT
NM_025137.3:c.442+137_442+138insCT	NP_079413.3:n.442+137_442+138insCT
XM_005254695.3:c.442+137_442+138insCT	XP_005254752.1:n.442+137_442+138insCT
XM_006720700.1:c.442+137_442+138insCT	XP_006720763.1:n.442+137_442+138insCT
XM_006720701.2:c.442+137_442+138insCT	XP_006720764.1:n.442+137_442+138insCT
XM_011522093.1:c.442+137_442+138insCT	XP_011520395.1:n.442+137_442+138insCT
XR_931917.1:n.473+137_473+138insCT
XM_006720701.3:c.442+137_442+138insCT	XP_006720764.1:n.442+137_442+138insCT
XM_017022634.1:c.442+137_442+138insCT	XP_016878123.1:n.442+137_442+138insCT
XM_017022635.2:c.442+137_442+138insCT	XP_016878124.1:n.442+137_442+138insCT
XR_001751402.1:n.473+137_473+138insCT
XR_931917.2:n.473+137_473+138insCT
NM_025137.4:c.442+137_442+138insCT MANE Select	NP_079413.3:n.442+137_442+138insCT
NM_001160227.2:c.442+137_442+138insCT	NP_001153699.1:n.442+137_442+138insCT