Canonical Allele Identifier: CA2173694799
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584041A= , CM000677.2:g.44584041A= GRCh38
NC_000015.9:g.44876239A= , CM000677.1:g.44876239A= GRCh37
NC_000015.8:g.42663531A= NCBI36
NG_008885.1:g.84638T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5639T= ENSP00000453246.2:p.Phe1880=
ENST00000561391.2:n.1867T=
ENST00000682065.1:c.5495T= ENSP00000507025.1:p.Phe1832=
ENST00000682460.1:c.*1896T= ENSP00000508334.1:n.*1896T=
ENST00000682495.1:c.*2131T= ENSP00000507166.1:n.*2131T=
ENST00000682669.1:c.5438T= ENSP00000507782.1:p.Phe1813=
ENST00000683186.1:c.*2402T= ENSP00000507268.1:n.*2402T=
ENST00000683496.1:c.5639T= ENSP00000506968.1:p.Phe1880=
ENST00000683734.1:c.5639T= ENSP00000508319.1:p.Phe1880=
ENST00000683753.1:n.4685T=
ENST00000684038.1:c.*2059T= ENSP00000507141.1:n.*2059T=
ENST00000684235.1:c.5639T= ENSP00000508295.1:p.Phe1880=
ENST00000684676.1:c.5516-106T= ENSP00000506948.1:n.5516-106T=
ENST00000261866.12:c.5639T= MANE Select ENSP00000261866.7:p.Phe1880=
ENST00000261866.11:c.5639T= ENSP00000261866.7:p.Phe1880=
ENST00000427534.6:c.5639T= ENSP00000396110.2:p.Phe1880=
ENST00000535302.6:c.5639T= ENSP00000445278.2:p.Phe1880=
ENST00000558319.5:c.5639T= ENSP00000453599.1:p.Phe1880=
ENST00000559511.5:c.487T=
ENST00000559822.1:c.288-106T=
NM_001160227.1:c.5639T= NP_001153699.1:p.Phe1880=
NM_025137.3:c.5639T= NP_079413.3:p.Phe1880=
XM_005254695.3:c.5381T= XP_005254752.1:p.Phe1794=
XM_006720700.1:c.5495T= XP_006720763.1:p.Phe1832=
XM_017022634.1:c.5639T= XP_016878123.1:p.Phe1880=
XM_017022636.1:c.2516T= XP_016878125.1:p.Phe839=
NM_025137.4:c.5639T= MANE Select NP_079413.3:p.Phe1880=
NM_001160227.2:c.5639T= NP_001153699.1:p.Phe1880=