Canonical Allele Identifier: CA2173686328
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584349G= , CM000677.2:g.44584349G= GRCh38
NC_000015.9:g.44876547G= , CM000677.1:g.44876547G= GRCh37
NC_000015.8:g.42663839G= NCBI36
NG_008885.1:g.84330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5331C= ENSP00000453246.2:p.Thr1777=
ENST00000561391.2:n.1559C=
ENST00000682065.1:c.5187C= ENSP00000507025.1:p.Thr1729=
ENST00000682460.1:c.*1588C= ENSP00000508334.1:n.*1588C=
ENST00000682495.1:c.*1823C= ENSP00000507166.1:n.*1823C=
ENST00000682669.1:c.5130C= ENSP00000507782.1:p.Thr1710=
ENST00000683186.1:c.*2094C= ENSP00000507268.1:n.*2094C=
ENST00000683496.1:c.5331C= ENSP00000506968.1:p.Thr1777=
ENST00000683734.1:c.5331C= ENSP00000508319.1:p.Thr1777=
ENST00000683753.1:n.4377C=
ENST00000684038.1:c.*1751C= ENSP00000507141.1:n.*1751C=
ENST00000684235.1:c.5331C= ENSP00000508295.1:p.Thr1777=
ENST00000684676.1:c.5331C= ENSP00000506948.1:p.Thr1777=
ENST00000261866.12:c.5331C= MANE Select ENSP00000261866.7:p.Thr1777=
ENST00000261866.11:c.5331C= ENSP00000261866.7:p.Thr1777=
ENST00000427534.6:c.5331C= ENSP00000396110.2:p.Thr1777=
ENST00000535302.6:c.5331C= ENSP00000445278.2:p.Thr1777=
ENST00000558319.5:c.5331C= ENSP00000453599.1:p.Thr1777=
ENST00000558790.5:n.768C=
ENST00000559511.5:c.179C=
ENST00000559822.1:c.103C=
NM_001160227.1:c.5331C= NP_001153699.1:p.Thr1777=
NM_025137.3:c.5331C= NP_079413.3:p.Thr1777=
XM_005254695.3:c.5073C= XP_005254752.1:p.Thr1691=
XM_006720700.1:c.5187C= XP_006720763.1:p.Thr1729=
XM_017022634.1:c.5331C= XP_016878123.1:p.Thr1777=
XM_017022636.1:c.2208C= XP_016878125.1:p.Thr736=
XR_931917.2:n.5385C=
NM_025137.4:c.5331C= MANE Select NP_079413.3:p.Thr1777=
NM_001160227.2:c.5331C= NP_001153699.1:p.Thr1777=