Canonical Allele Identifier: CA7534866

Gene: SPG11

Linked Data

• dbSNP Id: rs763169552
• ExAC: 15:44891039 AAAAG / A
• gnomAD v2: 15-44891039-AAAAG-A
• gnomAD v4: 15-44598841-AAAAG-A
• MyVariant Identifiers: chr15:g.44891040_44891043del (hg19) ; chr15:g.44598842_44598845del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598846_44598849del , CM000677.2:g.44598846_44598849del	GRCh38
NC_000015.9:g.44891044_44891047del , CM000677.1:g.44891044_44891047del	GRCh37
NC_000015.8:g.42678336_42678339del	NCBI36
NG_008885.1:g.69834_69837del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3687-9_3687-6del	ENSP00000453246.2:n.3687-9_3687-6del
ENST00000682065.1:c.3687-9_3687-6del	ENSP00000507025.1:n.3687-9_3687-6del
ENST00000682460.1:c.*107-9_*107-6del	ENSP00000508334.1:n.*107-9_*107-6del
ENST00000682495.1:c.*179-9_*179-6del	ENSP00000507166.1:n.*179-9_*179-6del
ENST00000682669.1:c.3486-9_3486-6del	ENSP00000507782.1:n.3486-9_3486-6del
ENST00000682788.1:c.3687-9_3687-6del	ENSP00000508089.1:n.3687-9_3687-6del
ENST00000682915.1:c.3780-9_3780-6del	ENSP00000507493.1:n.3780-9_3780-6del
ENST00000683121.1:c.3687-9_3687-6del	ENSP00000507557.1:n.3687-9_3687-6del
ENST00000683186.1:c.*450-9_*450-6del	ENSP00000507268.1:n.*450-9_*450-6del
ENST00000683496.1:c.3687-9_3687-6del	ENSP00000506968.1:n.3687-9_3687-6del
ENST00000683734.1:c.3687-9_3687-6del	ENSP00000508319.1:n.3687-9_3687-6del
ENST00000683753.1:n.2733-9_2733-6del
ENST00000683838.1:n.761-9_761-6del
ENST00000684038.1:c.*107-9_*107-6del	ENSP00000507141.1:n.*107-9_*107-6del
ENST00000684235.1:c.3687-9_3687-6del	ENSP00000508295.1:n.3687-9_3687-6del
ENST00000684676.1:c.3687-9_3687-6del	ENSP00000506948.1:n.3687-9_3687-6del
ENST00000261866.12:c.3687-9_3687-6del MANE Select	ENSP00000261866.7:n.3687-9_3687-6del
ENST00000261866.11:c.3687-9_3687-6del	ENSP00000261866.7:n.3687-9_3687-6del
ENST00000427534.6:c.3687-9_3687-6del	ENSP00000396110.2:n.3687-9_3687-6del
ENST00000535302.6:c.3687-9_3687-6del	ENSP00000445278.2:n.3687-9_3687-6del
ENST00000558093.1:n.301-9_301-6del
ENST00000558319.5:c.3687-9_3687-6del	ENSP00000453599.1:n.3687-9_3687-6del
NM_001160227.1:c.3687-9_3687-6del	NP_001153699.1:n.3687-9_3687-6del
NM_025137.3:c.3687-9_3687-6del	NP_079413.3:n.3687-9_3687-6del
XM_005254695.3:c.3429-9_3429-6del	XP_005254752.1:n.3429-9_3429-6del
XM_006720700.1:c.3687-9_3687-6del	XP_006720763.1:n.3687-9_3687-6del
XM_006720701.2:c.3687-9_3687-6del	XP_006720764.1:n.3687-9_3687-6del
XM_011522093.1:c.3687-472_3687-469del	XP_011520395.1:n.3687-472_3687-469del
XR_931917.1:n.3718-9_3718-6del
XM_006720701.3:c.3687-9_3687-6del	XP_006720764.1:n.3687-9_3687-6del
XM_017022634.1:c.3687-9_3687-6del	XP_016878123.1:n.3687-9_3687-6del
XM_017022635.2:c.3687-9_3687-6del	XP_016878124.1:n.3687-9_3687-6del
XM_017022636.1:c.564-9_564-6del	XP_016878125.1:n.564-9_564-6del
XR_001751402.1:n.3718-472_3718-469del
XR_931917.2:n.3718-9_3718-6del
NM_025137.4:c.3687-9_3687-6del MANE Select	NP_079413.3:n.3687-9_3687-6del
NM_001160227.2:c.3687-9_3687-6del	NP_001153699.1:n.3687-9_3687-6del