Canonical Allele Identifier: CA2628202111
Gene: SPG11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44567363_44567367dup , CM000677.2:g.44567363_44567367dup GRCh38
NC_000015.9:g.44859561_44859565dup , CM000677.1:g.44859561_44859565dup GRCh37
NC_000015.8:g.42646853_42646857dup NCBI36
NG_008885.1:g.101325_101329dup

Transcript Alleles

HGVS Amino-acid change
ENST00000558138.2:c.445+70_445+74dup ENSP00000453314.2:n.445+70_445+74dup
ENST00000559511.6:c.6277+70_6277+74dup ENSP00000453246.2:n.6277+70_6277+74dup
ENST00000682065.1:c.6610+70_6610+74dup ENSP00000507025.1:n.6610+70_6610+74dup
ENST00000682460.1:c.*3011+70_*3011+74dup ENSP00000508334.1:n.*3011+70_*3011+74dup
ENST00000682495.1:c.*3246+70_*3246+74dup ENSP00000507166.1:n.*3246+70_*3246+74dup
ENST00000682669.1:c.6553+70_6553+74dup ENSP00000507782.1:n.6553+70_6553+74dup
ENST00000683186.1:c.*3517+70_*3517+74dup ENSP00000507268.1:n.*3517+70_*3517+74dup
ENST00000683496.1:c.*396+70_*396+74dup ENSP00000506968.1:n.*396+70_*396+74dup
ENST00000683734.1:c.*704+70_*704+74dup ENSP00000508319.1:n.*704+70_*704+74dup
ENST00000683753.1:n.5800+70_5800+74dup
ENST00000684038.1:c.*3174+70_*3174+74dup ENSP00000507141.1:n.*3174+70_*3174+74dup
ENST00000684235.1:c.6754+70_6754+74dup ENSP00000508295.1:n.6754+70_6754+74dup
ENST00000261866.12:c.6754+70_6754+74dup MANE Select ENSP00000261866.7:n.6754+70_6754+74dup
ENST00000261866.11:c.6754+70_6754+74dup ENSP00000261866.7:n.6754+70_6754+74dup
ENST00000427534.6:c.6754+70_6754+74dup ENSP00000396110.2:n.6754+70_6754+74dup
ENST00000535302.6:c.6415+70_6415+74dup ENSP00000445278.2:n.6415+70_6415+74dup
ENST00000558138.1:c.445+70_445+74dup ENSP00000453314.1:n.445+70_445+74dup
ENST00000559347.1:n.583+70_583+74dup
ENST00000559511.5:c.1125+70_1125+74dup
ENST00000561268.5:n.514_518dup
NM_001160227.1:c.6415+70_6415+74dup NP_001153699.1:n.6415+70_6415+74dup
NM_025137.3:c.6754+70_6754+74dup NP_079413.3:n.6754+70_6754+74dup
XM_005254695.3:c.6496+70_6496+74dup XP_005254752.1:n.6496+70_6496+74dup
XM_006720700.1:c.6610+70_6610+74dup XP_006720763.1:n.6610+70_6610+74dup
XM_017022634.1:c.6646+70_6646+74dup XP_016878123.1:n.6646+70_6646+74dup
XM_017022636.1:c.3631+70_3631+74dup XP_016878125.1:n.3631+70_3631+74dup
NM_025137.4:c.6754+70_6754+74dup MANE Select NP_079413.3:n.6754+70_6754+74dup
NM_001160227.2:c.6415+70_6415+74dup NP_001153699.1:n.6415+70_6415+74dup