Canonical Allele Identifier: CA915948965
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44574921_44574924dup , CM000677.2:g.44574921_44574924dup GRCh38
NC_000015.9:g.44867119_44867122dup , CM000677.1:g.44867119_44867122dup GRCh37
NC_000015.8:g.42654411_42654414dup NCBI36
NG_008885.1:g.93760_93763dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5867-4261_5867-4258dup ENSP00000453246.2:n.5867-4261_5867-4258dup
ENST00000561391.2:n.2217_2220dup
ENST00000682065.1:c.5845_5848dup ENSP00000507025.1:p.Tyr1950SerfsTer3
ENST00000682460.1:c.*2246_*2249dup ENSP00000508334.1:n.*2246_*2249dup
ENST00000682495.1:c.*2481_*2484dup ENSP00000507166.1:n.*2481_*2484dup
ENST00000682669.1:c.5788_5791dup ENSP00000507782.1:p.Tyr1931SerfsTer3
ENST00000683186.1:c.*2752_*2755dup ENSP00000507268.1:n.*2752_*2755dup
ENST00000683496.1:c.5989_5992dup ENSP00000506968.1:p.Tyr1998SerfsTer3
ENST00000683734.1:c.5867-1174_5867-1171dup ENSP00000508319.1:n.5867-1174_5867-1171dup
ENST00000683753.1:n.5035_5038dup
ENST00000684038.1:c.*2409_*2412dup ENSP00000507141.1:n.*2409_*2412dup
ENST00000684235.1:c.5989_5992dup ENSP00000508295.1:p.Tyr1998SerfsTer3
ENST00000684676.1:c.*138_*141dup ENSP00000506948.1:n.*138_*141dup
ENST00000261866.12:c.5989_5992dup MANE Select ENSP00000261866.7:p.Tyr1998SerfsTer3
ENST00000261866.11:c.5989_5992dup ENSP00000261866.7:p.Tyr1998SerfsTer3
ENST00000427534.6:c.5989_5992dup ENSP00000396110.2:p.Tyr1998SerfsTer3
ENST00000535302.6:c.5867-2099_5867-2096dup ENSP00000445278.2:n.5867-2099_5867-2096dup
ENST00000558080.1:n.354_357dup
ENST00000558319.5:c.5989_5992dup ENSP00000453599.1:p.Tyr1998SerfsTer3
ENST00000559511.5:c.715-4261_715-4258dup
ENST00000559822.1:c.532_535dup
NM_001160227.1:c.5867-2099_5867-2096dup NP_001153699.1:n.5867-2099_5867-2096dup
NM_025137.3:c.5989_5992dup NP_079413.3:p.Tyr1998SerfsTer3
XM_005254695.3:c.5731_5734dup XP_005254752.1:p.Tyr1912SerfsTer3
XM_006720700.1:c.5845_5848dup XP_006720763.1:p.Tyr1950SerfsTer3
XM_017022634.1:c.5989_5992dup XP_016878123.1:p.Tyr1998SerfsTer3
XM_017022636.1:c.2866_2869dup XP_016878125.1:p.Tyr957SerfsTer3
NM_025137.4:c.5989_5992dup MANE Select NP_079413.3:p.Tyr1998SerfsTer3
NM_001160227.2:c.5867-2099_5867-2096dup NP_001153699.1:n.5867-2099_5867-2096dup