Canonical Allele Identifier: CA2173686834
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584555T= , CM000677.2:g.44584555T= GRCh38
NC_000015.9:g.44876753T= , CM000677.1:g.44876753T= GRCh37
NC_000015.8:g.42664045T= NCBI36
NG_008885.1:g.84124A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5125A= ENSP00000453246.2:p.Thr1709=
ENST00000561391.2:n.1353A=
ENST00000682065.1:c.5122-141A= ENSP00000507025.1:n.5122-141A=
ENST00000682460.1:c.*1382A= ENSP00000508334.1:n.*1382A=
ENST00000682495.1:c.*1617A= ENSP00000507166.1:n.*1617A=
ENST00000682669.1:c.4924A= ENSP00000507782.1:p.Thr1642=
ENST00000683186.1:c.*1888A= ENSP00000507268.1:n.*1888A=
ENST00000683496.1:c.5125A= ENSP00000506968.1:p.Thr1709=
ENST00000683734.1:c.5125A= ENSP00000508319.1:p.Thr1709=
ENST00000683753.1:n.4171A=
ENST00000684038.1:c.*1545A= ENSP00000507141.1:n.*1545A=
ENST00000684235.1:c.5125A= ENSP00000508295.1:p.Thr1709=
ENST00000684676.1:c.5125A= ENSP00000506948.1:p.Thr1709=
ENST00000261866.12:c.5125A= MANE Select ENSP00000261866.7:p.Thr1709=
ENST00000261866.11:c.5125A= ENSP00000261866.7:p.Thr1709=
ENST00000427534.6:c.5125A= ENSP00000396110.2:p.Thr1709=
ENST00000535302.6:c.5125A= ENSP00000445278.2:p.Thr1709=
ENST00000558319.5:c.5125A= ENSP00000453599.1:p.Thr1709=
ENST00000558790.5:n.562A=
NM_001160227.1:c.5125A= NP_001153699.1:p.Thr1709=
NM_025137.3:c.5125A= NP_079413.3:p.Thr1709=
XM_005254695.3:c.4867A= XP_005254752.1:p.Thr1623=
XM_006720700.1:c.5122-141A= XP_006720763.1:n.5122-141A=
XM_017022634.1:c.5125A= XP_016878123.1:p.Thr1709=
XM_017022636.1:c.2002A= XP_016878125.1:p.Thr668=
XR_931917.2:n.5179A=
NM_025137.4:c.5125A= MANE Select NP_079413.3:p.Thr1709=
NM_001160227.2:c.5125A= NP_001153699.1:p.Thr1709=