Canonical Allele Identifier: CA2628203073

Gene: SPG11

Linked Data

• gnomAD v4: 15-44575164-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575166_44575167del , CM000677.2:g.44575166_44575167del	GRCh38
NC_000015.9:g.44867364_44867365del , CM000677.1:g.44867364_44867365del	GRCh37
NC_000015.8:g.42654656_42654657del	NCBI36
NG_008885.1:g.93513_93514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4508_5867-4507del	ENSP00000453246.2:n.5867-4508_5867-4507del
ENST00000561391.2:n.2095-125_2095-124del
ENST00000682065.1:c.5723-125_5723-124del	ENSP00000507025.1:n.5723-125_5723-124del
ENST00000682460.1:c.*2124-125_*2124-124del	ENSP00000508334.1:n.*2124-125_*2124-124del
ENST00000682495.1:c.*2359-125_*2359-124del	ENSP00000507166.1:n.*2359-125_*2359-124del
ENST00000682669.1:c.5666-125_5666-124del	ENSP00000507782.1:n.5666-125_5666-124del
ENST00000683186.1:c.*2630-125_*2630-124del	ENSP00000507268.1:n.*2630-125_*2630-124del
ENST00000683496.1:c.5867-125_5867-124del	ENSP00000506968.1:n.5867-125_5867-124del
ENST00000683734.1:c.5867-1421_5867-1420del	ENSP00000508319.1:n.5867-1421_5867-1420del
ENST00000683753.1:n.4913-125_4913-124del
ENST00000684038.1:c.*2287-125_*2287-124del	ENSP00000507141.1:n.*2287-125_*2287-124del
ENST00000684235.1:c.5867-125_5867-124del	ENSP00000508295.1:n.5867-125_5867-124del
ENST00000684676.1:c.*16-125_*16-124del	ENSP00000506948.1:n.*16-125_*16-124del
ENST00000261866.12:c.5867-125_5867-124del MANE Select	ENSP00000261866.7:n.5867-125_5867-124del
ENST00000261866.11:c.5867-125_5867-124del	ENSP00000261866.7:n.5867-125_5867-124del
ENST00000427534.6:c.5867-125_5867-124del	ENSP00000396110.2:n.5867-125_5867-124del
ENST00000535302.6:c.5867-2346_5867-2345del	ENSP00000445278.2:n.5867-2346_5867-2345del
ENST00000558080.1:n.107_108del
ENST00000558319.5:c.5867-125_5867-124del	ENSP00000453599.1:n.5867-125_5867-124del
ENST00000559511.5:c.715-4508_715-4507del
ENST00000559822.1:c.410-125_410-124del
NM_001160227.1:c.5867-2346_5867-2345del	NP_001153699.1:n.5867-2346_5867-2345del
NM_025137.3:c.5867-125_5867-124del	NP_079413.3:n.5867-125_5867-124del
XM_005254695.3:c.5609-125_5609-124del	XP_005254752.1:n.5609-125_5609-124del
XM_006720700.1:c.5723-125_5723-124del	XP_006720763.1:n.5723-125_5723-124del
XM_017022634.1:c.5867-125_5867-124del	XP_016878123.1:n.5867-125_5867-124del
XM_017022636.1:c.2744-125_2744-124del	XP_016878125.1:n.2744-125_2744-124del
NM_025137.4:c.5867-125_5867-124del MANE Select	NP_079413.3:n.5867-125_5867-124del
NM_001160227.2:c.5867-2346_5867-2345del	NP_001153699.1:n.5867-2346_5867-2345del