Canonical Allele Identifier: CA2173686292
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584330C= , CM000677.2:g.44584330C= GRCh38
NC_000015.9:g.44876528C= , CM000677.1:g.44876528C= GRCh37
NC_000015.8:g.42663820C= NCBI36
NG_008885.1:g.84349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5350G= ENSP00000453246.2:p.Ala1784=
ENST00000561391.2:n.1578G=
ENST00000682065.1:c.5206G= ENSP00000507025.1:p.Ala1736=
ENST00000682460.1:c.*1607G= ENSP00000508334.1:n.*1607G=
ENST00000682495.1:c.*1842G= ENSP00000507166.1:n.*1842G=
ENST00000682669.1:c.5149G= ENSP00000507782.1:p.Ala1717=
ENST00000683186.1:c.*2113G= ENSP00000507268.1:n.*2113G=
ENST00000683496.1:c.5350G= ENSP00000506968.1:p.Ala1784=
ENST00000683734.1:c.5350G= ENSP00000508319.1:p.Ala1784=
ENST00000683753.1:n.4396G=
ENST00000684038.1:c.*1770G= ENSP00000507141.1:n.*1770G=
ENST00000684235.1:c.5350G= ENSP00000508295.1:p.Ala1784=
ENST00000684676.1:c.5350G= ENSP00000506948.1:p.Ala1784=
ENST00000261866.12:c.5350G= MANE Select ENSP00000261866.7:p.Ala1784=
ENST00000261866.11:c.5350G= ENSP00000261866.7:p.Ala1784=
ENST00000427534.6:c.5350G= ENSP00000396110.2:p.Ala1784=
ENST00000535302.6:c.5350G= ENSP00000445278.2:p.Ala1784=
ENST00000558319.5:c.5350G= ENSP00000453599.1:p.Ala1784=
ENST00000558790.5:n.787G=
ENST00000559511.5:c.198G=
ENST00000559822.1:c.122G=
NM_001160227.1:c.5350G= NP_001153699.1:p.Ala1784=
NM_025137.3:c.5350G= NP_079413.3:p.Ala1784=
XM_005254695.3:c.5092G= XP_005254752.1:p.Ala1698=
XM_006720700.1:c.5206G= XP_006720763.1:p.Ala1736=
XM_017022634.1:c.5350G= XP_016878123.1:p.Ala1784=
XM_017022636.1:c.2227G= XP_016878125.1:p.Ala743=
XR_931917.2:n.5404G=
NM_025137.4:c.5350G= MANE Select NP_079413.3:p.Ala1784=
NM_001160227.2:c.5350G= NP_001153699.1:p.Ala1784=