Canonical Allele Identifier: CA7534422
Gene: SPG11 HGNC NCBI

Linked Data

ClinVar Variation Id: 374112
dbSNP Id: rs201689565

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44584299A>G , CM000677.2:g.44584299A>G GRCh38
NC_000015.9:g.44876497A>G , CM000677.1:g.44876497A>G GRCh37
NC_000015.8:g.42663789A>G NCBI36
NG_008885.1:g.84380T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.5381T>C ENSP00000453246.2:p.Leu1794Pro
ENST00000561391.2:n.1609T>C
ENST00000682065.1:c.5237T>C ENSP00000507025.1:p.Leu1746Pro
ENST00000682460.1:c.*1638T>C ENSP00000508334.1:n.*1638T>C
ENST00000682495.1:c.*1873T>C ENSP00000507166.1:n.*1873T>C
ENST00000682669.1:c.5180T>C ENSP00000507782.1:p.Leu1727Pro
ENST00000683186.1:c.*2144T>C ENSP00000507268.1:n.*2144T>C
ENST00000683496.1:c.5381T>C ENSP00000506968.1:p.Leu1794Pro
ENST00000683734.1:c.5381T>C ENSP00000508319.1:p.Leu1794Pro
ENST00000683753.1:n.4427T>C
ENST00000684038.1:c.*1801T>C ENSP00000507141.1:n.*1801T>C
ENST00000684235.1:c.5381T>C ENSP00000508295.1:p.Leu1794Pro
ENST00000684676.1:c.5381T>C ENSP00000506948.1:p.Leu1794Pro
ENST00000261866.12:c.5381T>C MANE Select ENSP00000261866.7:p.Leu1794Pro
ENST00000261866.11:c.5381T>C ENSP00000261866.7:p.Leu1794Pro
ENST00000427534.6:c.5381T>C ENSP00000396110.2:p.Leu1794Pro
ENST00000535302.6:c.5381T>C ENSP00000445278.2:p.Leu1794Pro
ENST00000558319.5:c.5381T>C ENSP00000453599.1:p.Leu1794Pro
ENST00000558790.5:n.818T>C
ENST00000559511.5:c.229T>C
ENST00000559822.1:c.153T>C
NM_001160227.1:c.5381T>C NP_001153699.1:p.Leu1794Pro
NM_025137.3:c.5381T>C NP_079413.3:p.Leu1794Pro
XM_005254695.3:c.5123T>C XP_005254752.1:p.Leu1708Pro
XM_006720700.1:c.5237T>C XP_006720763.1:p.Leu1746Pro
XM_017022634.1:c.5381T>C XP_016878123.1:p.Leu1794Pro
XM_017022636.1:c.2258T>C XP_016878125.1:p.Leu753Pro
XR_931917.2:n.5435T>C
NM_025137.4:c.5381T>C MANE Select NP_079413.3:p.Leu1794Pro
NM_001160227.2:c.5381T>C NP_001153699.1:p.Leu1794Pro