Canonical Allele Identifier: CA2173686400
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584389G= , CM000677.2:g.44584389G= GRCh38
NC_000015.9:g.44876587G= , CM000677.1:g.44876587G= GRCh37
NC_000015.8:g.42663879G= NCBI36
NG_008885.1:g.84290C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5291C= ENSP00000453246.2:p.Thr1764=
ENST00000561391.2:n.1519C=
ENST00000682065.1:c.5147C= ENSP00000507025.1:p.Thr1716=
ENST00000682460.1:c.*1548C= ENSP00000508334.1:n.*1548C=
ENST00000682495.1:c.*1783C= ENSP00000507166.1:n.*1783C=
ENST00000682669.1:c.5090C= ENSP00000507782.1:p.Thr1697=
ENST00000683186.1:c.*2054C= ENSP00000507268.1:n.*2054C=
ENST00000683496.1:c.5291C= ENSP00000506968.1:p.Thr1764=
ENST00000683734.1:c.5291C= ENSP00000508319.1:p.Thr1764=
ENST00000683753.1:n.4337C=
ENST00000684038.1:c.*1711C= ENSP00000507141.1:n.*1711C=
ENST00000684235.1:c.5291C= ENSP00000508295.1:p.Thr1764=
ENST00000684676.1:c.5291C= ENSP00000506948.1:p.Thr1764=
ENST00000261866.12:c.5291C= MANE Select ENSP00000261866.7:p.Thr1764=
ENST00000261866.11:c.5291C= ENSP00000261866.7:p.Thr1764=
ENST00000427534.6:c.5291C= ENSP00000396110.2:p.Thr1764=
ENST00000535302.6:c.5291C= ENSP00000445278.2:p.Thr1764=
ENST00000558319.5:c.5291C= ENSP00000453599.1:p.Thr1764=
ENST00000558790.5:n.728C=
ENST00000559511.5:c.139C=
ENST00000559822.1:c.63C=
NM_001160227.1:c.5291C= NP_001153699.1:p.Thr1764=
NM_025137.3:c.5291C= NP_079413.3:p.Thr1764=
XM_005254695.3:c.5033C= XP_005254752.1:p.Thr1678=
XM_006720700.1:c.5147C= XP_006720763.1:p.Thr1716=
XM_017022634.1:c.5291C= XP_016878123.1:p.Thr1764=
XM_017022636.1:c.2168C= XP_016878125.1:p.Thr723=
XR_931917.2:n.5345C=
NM_025137.4:c.5291C= MANE Select NP_079413.3:p.Thr1764=
NM_001160227.2:c.5291C= NP_001153699.1:p.Thr1764=