Canonical Allele Identifier: CA2173686948

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584604_44584605delinsAG , CM000677.2:g.44584604_44584605delinsAG	GRCh38
NC_000015.9:g.44876802_44876803delinsAG , CM000677.1:g.44876802_44876803delinsAG	GRCh37
NC_000015.8:g.42664094_42664095delinsAG	NCBI36
NG_008885.1:g.84074_84075delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5122-47_5122-46delinsCT	ENSP00000453246.2:n.5122-47_5122-46delinsCT
ENST00000561391.2:n.1350-47_1350-46delinsCT
ENST00000682065.1:c.5122-191_5122-190delinsCT	ENSP00000507025.1:n.5122-191_5122-190delinsCT
ENST00000682460.1:c.*1379-47_*1379-46delinsCT	ENSP00000508334.1:n.*1379-47_*1379-46delinsCT
ENST00000682495.1:c.*1614-47_*1614-46delinsCT	ENSP00000507166.1:n.*1614-47_*1614-46delinsCT
ENST00000682669.1:c.4921-47_4921-46delinsCT	ENSP00000507782.1:n.4921-47_4921-46delinsCT
ENST00000683186.1:c.*1885-47_*1885-46delinsCT	ENSP00000507268.1:n.*1885-47_*1885-46delinsCT
ENST00000683496.1:c.5122-47_5122-46delinsCT	ENSP00000506968.1:n.5122-47_5122-46delinsCT
ENST00000683734.1:c.5122-47_5122-46delinsCT	ENSP00000508319.1:n.5122-47_5122-46delinsCT
ENST00000683753.1:n.4168-47_4168-46delinsCT
ENST00000684038.1:c.*1542-47_*1542-46delinsCT	ENSP00000507141.1:n.*1542-47_*1542-46delinsCT
ENST00000684235.1:c.5122-47_5122-46delinsCT	ENSP00000508295.1:n.5122-47_5122-46delinsCT
ENST00000684676.1:c.5122-47_5122-46delinsCT	ENSP00000506948.1:n.5122-47_5122-46delinsCT
ENST00000261866.12:c.5122-47_5122-46delinsCT MANE Select	ENSP00000261866.7:n.5122-47_5122-46delinsCT
ENST00000261866.11:c.5122-47_5122-46delinsCT	ENSP00000261866.7:n.5122-47_5122-46delinsCT
ENST00000427534.6:c.5122-47_5122-46delinsCT	ENSP00000396110.2:n.5122-47_5122-46delinsCT
ENST00000535302.6:c.5122-47_5122-46delinsCT	ENSP00000445278.2:n.5122-47_5122-46delinsCT
ENST00000558319.5:c.5122-47_5122-46delinsCT	ENSP00000453599.1:n.5122-47_5122-46delinsCT
ENST00000558790.5:n.559-47_559-46delinsCT
NM_001160227.1:c.5122-47_5122-46delinsCT	NP_001153699.1:n.5122-47_5122-46delinsCT
NM_025137.3:c.5122-47_5122-46delinsCT	NP_079413.3:n.5122-47_5122-46delinsCT
XM_005254695.3:c.4864-47_4864-46delinsCT	XP_005254752.1:n.4864-47_4864-46delinsCT
XM_006720700.1:c.5122-191_5122-190delinsCT	XP_006720763.1:n.5122-191_5122-190delinsCT
XM_017022634.1:c.5122-47_5122-46delinsCT	XP_016878123.1:n.5122-47_5122-46delinsCT
XM_017022636.1:c.1999-47_1999-46delinsCT	XP_016878125.1:n.1999-47_1999-46delinsCT
XR_931917.2:n.5176-47_5176-46delinsCT
NM_025137.4:c.5122-47_5122-46delinsCT MANE Select	NP_079413.3:n.5122-47_5122-46delinsCT
NM_001160227.2:c.5122-47_5122-46delinsCT	NP_001153699.1:n.5122-47_5122-46delinsCT