Canonical Allele Identifier: CA713054610
Gene: SPG11 HGNC NCBI

Linked Data

dbSNP Id: rs1161524954

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44575082G>C , CM000677.2:g.44575082G>C GRCh38
NC_000015.9:g.44867280G>C , CM000677.1:g.44867280G>C GRCh37
NC_000015.8:g.42654572G>C NCBI36
NG_008885.1:g.93597C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5867-4424C>G ENSP00000453246.2:n.5867-4424C>G
ENST00000561391.2:n.2095-41C>G
ENST00000682065.1:c.5723-41C>G ENSP00000507025.1:n.5723-41C>G
ENST00000682460.1:c.*2124-41C>G ENSP00000508334.1:n.*2124-41C>G
ENST00000682495.1:c.*2359-41C>G ENSP00000507166.1:n.*2359-41C>G
ENST00000682669.1:c.5666-41C>G ENSP00000507782.1:n.5666-41C>G
ENST00000683186.1:c.*2630-41C>G ENSP00000507268.1:n.*2630-41C>G
ENST00000683496.1:c.5867-41C>G ENSP00000506968.1:n.5867-41C>G
ENST00000683734.1:c.5867-1337C>G ENSP00000508319.1:n.5867-1337C>G
ENST00000683753.1:n.4913-41C>G
ENST00000684038.1:c.*2287-41C>G ENSP00000507141.1:n.*2287-41C>G
ENST00000684235.1:c.5867-41C>G ENSP00000508295.1:n.5867-41C>G
ENST00000684676.1:c.*16-41C>G ENSP00000506948.1:n.*16-41C>G
ENST00000261866.12:c.5867-41C>G MANE Select ENSP00000261866.7:n.5867-41C>G
ENST00000261866.11:c.5867-41C>G ENSP00000261866.7:n.5867-41C>G
ENST00000427534.6:c.5867-41C>G ENSP00000396110.2:n.5867-41C>G
ENST00000535302.6:c.5867-2262C>G ENSP00000445278.2:n.5867-2262C>G
ENST00000558080.1:n.191C>G
ENST00000558319.5:c.5867-41C>G ENSP00000453599.1:n.5867-41C>G
ENST00000559511.5:c.715-4424C>G
ENST00000559822.1:c.410-41C>G
NM_001160227.1:c.5867-2262C>G NP_001153699.1:n.5867-2262C>G
NM_025137.3:c.5867-41C>G NP_079413.3:n.5867-41C>G
XM_005254695.3:c.5609-41C>G XP_005254752.1:n.5609-41C>G
XM_006720700.1:c.5723-41C>G XP_006720763.1:n.5723-41C>G
XM_017022634.1:c.5867-41C>G XP_016878123.1:n.5867-41C>G
XM_017022636.1:c.2744-41C>G XP_016878125.1:n.2744-41C>G
NM_025137.4:c.5867-41C>G MANE Select NP_079413.3:n.5867-41C>G
NM_001160227.2:c.5867-2262C>G NP_001153699.1:n.5867-2262C>G