Canonical Allele Identifier: CA235929

Gene: SPG11

Linked Data

• ClinVar Variation Id: 188250
• ClinVar RCV Id: RCV000168213 ; RCV000171235
• dbSNP Id: rs786204176
• gnomAD v4: 15-44615524-G-T
• MyVariant Identifiers: chr15:g.44907722G>T (hg19) ; chr15:g.44615524G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44615524G>T , CM000677.2:g.44615524G>T	GRCh38
NC_000015.9:g.44907722G>T , CM000677.1:g.44907722G>T	GRCh37
NC_000015.8:g.42695014G>T	NCBI36
NG_008885.1:g.53155C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.2877C>A	ENSP00000453246.2:p.Cys959Ter
ENST00000682065.1:c.2877C>A	ENSP00000507025.1:p.Cys959Ter
ENST00000682460.1:c.2877C>A	ENSP00000508334.1:p.Cys959Ter
ENST00000682495.1:c.2877C>A	ENSP00000507166.1:p.Cys959Ter
ENST00000682669.1:c.2877C>A	ENSP00000507782.1:p.Cys959Ter
ENST00000682788.1:c.2877C>A	ENSP00000508089.1:p.Cys959Ter
ENST00000682915.1:c.2877C>A	ENSP00000507493.1:p.Cys959Ter
ENST00000683121.1:c.2877C>A	ENSP00000507557.1:p.Cys959Ter
ENST00000683186.1:c.2877C>A	ENSP00000507268.1:p.Cys959Ter
ENST00000683255.1:c.2877C>A	ENSP00000508340.1:p.Cys959Ter
ENST00000683496.1:c.2877C>A	ENSP00000506968.1:p.Cys959Ter
ENST00000683573.1:c.*92C>A	ENSP00000508031.1:n.*92C>A
ENST00000683734.1:c.2877C>A	ENSP00000508319.1:p.Cys959Ter
ENST00000683753.1:n.2001C>A
ENST00000684038.1:c.2619C>A	ENSP00000507141.1:p.Cys873Ter
ENST00000684235.1:c.2877C>A	ENSP00000508295.1:p.Cys959Ter
ENST00000684676.1:c.2877C>A	ENSP00000506948.1:p.Cys959Ter
ENST00000261866.12:c.2877C>A MANE Select	ENSP00000261866.7:p.Cys959Ter
ENST00000261866.11:c.2877C>A	ENSP00000261866.7:p.Cys959Ter
ENST00000427534.6:c.2877C>A	ENSP00000396110.2:p.Cys959Ter
ENST00000535302.6:c.2877C>A	ENSP00000445278.2:p.Cys959Ter
ENST00000558319.5:c.2877C>A	ENSP00000453599.1:p.Cys959Ter
ENST00000558989.1:n.1720C>A
ENST00000560435.1:c.224C>A	ENSP00000452629.1:n.224C>A
NM_001160227.1:c.2877C>A	NP_001153699.1:p.Cys959Ter
NM_025137.3:c.2877C>A	NP_079413.3:p.Cys959Ter
XM_005254695.3:c.2619C>A	XP_005254752.1:p.Cys873Ter
XM_006720700.1:c.2877C>A	XP_006720763.1:p.Cys959Ter
XM_006720701.2:c.2877C>A	XP_006720764.1:p.Cys959Ter
XM_011522093.1:c.2877C>A	XP_011520395.1:p.Cys959Ter
XR_931917.1:n.2908C>A
XM_006720701.3:c.2877C>A	XP_006720764.1:p.Cys959Ter
XM_017022634.1:c.2877C>A	XP_016878123.1:p.Cys959Ter
XM_017022635.2:c.2877C>A	XP_016878124.1:p.Cys959Ter
XM_017022636.1:c.-140C>A	XP_016878125.1:n.-140C>A
XR_001751402.1:n.2908C>A
XR_931917.2:n.2908C>A
NM_025137.4:c.2877C>A MANE Select	NP_079413.3:p.Cys959Ter
NM_001160227.2:c.2877C>A	NP_001153699.1:p.Cys959Ter