Canonical Allele Identifier: CA2528508051

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584588_44584589del , CM000677.2:g.44584588_44584589del	GRCh38
NC_000015.9:g.44876786_44876787del , CM000677.1:g.44876786_44876787del	GRCh37
NC_000015.8:g.42664078_42664079del	NCBI36
NG_008885.1:g.84090_84091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5122-31_5122-30del	ENSP00000453246.2:n.5122-31_5122-30del
ENST00000561391.2:n.1350-31_1350-30del
ENST00000682065.1:c.5122-175_5122-174del	ENSP00000507025.1:n.5122-175_5122-174del
ENST00000682460.1:c.*1379-31_*1379-30del	ENSP00000508334.1:n.*1379-31_*1379-30del
ENST00000682495.1:c.*1614-31_*1614-30del	ENSP00000507166.1:n.*1614-31_*1614-30del
ENST00000682669.1:c.4921-31_4921-30del	ENSP00000507782.1:n.4921-31_4921-30del
ENST00000683186.1:c.*1885-31_*1885-30del	ENSP00000507268.1:n.*1885-31_*1885-30del
ENST00000683496.1:c.5122-31_5122-30del	ENSP00000506968.1:n.5122-31_5122-30del
ENST00000683734.1:c.5122-31_5122-30del	ENSP00000508319.1:n.5122-31_5122-30del
ENST00000683753.1:n.4168-31_4168-30del
ENST00000684038.1:c.*1542-31_*1542-30del	ENSP00000507141.1:n.*1542-31_*1542-30del
ENST00000684235.1:c.5122-31_5122-30del	ENSP00000508295.1:n.5122-31_5122-30del
ENST00000684676.1:c.5122-31_5122-30del	ENSP00000506948.1:n.5122-31_5122-30del
ENST00000261866.12:c.5122-31_5122-30del MANE Select	ENSP00000261866.7:n.5122-31_5122-30del
ENST00000261866.11:c.5122-31_5122-30del	ENSP00000261866.7:n.5122-31_5122-30del
ENST00000427534.6:c.5122-31_5122-30del	ENSP00000396110.2:n.5122-31_5122-30del
ENST00000535302.6:c.5122-31_5122-30del	ENSP00000445278.2:n.5122-31_5122-30del
ENST00000558319.5:c.5122-31_5122-30del	ENSP00000453599.1:n.5122-31_5122-30del
ENST00000558790.5:n.559-31_559-30del
NM_001160227.1:c.5122-31_5122-30del	NP_001153699.1:n.5122-31_5122-30del
NM_025137.3:c.5122-31_5122-30del	NP_079413.3:n.5122-31_5122-30del
XM_005254695.3:c.4864-31_4864-30del	XP_005254752.1:n.4864-31_4864-30del
XM_006720700.1:c.5122-175_5122-174del	XP_006720763.1:n.5122-175_5122-174del
XM_017022634.1:c.5122-31_5122-30del	XP_016878123.1:n.5122-31_5122-30del
XM_017022636.1:c.1999-31_1999-30del	XP_016878125.1:n.1999-31_1999-30del
XR_931917.2:n.5176-31_5176-30del
NM_025137.4:c.5122-31_5122-30del MANE Select	NP_079413.3:n.5122-31_5122-30del
NM_001160227.2:c.5122-31_5122-30del	NP_001153699.1:n.5122-31_5122-30del