Canonical Allele Identifier: CA392230378
Gene: SPG11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44598793A>G , CM000677.2:g.44598793A>G GRCh38
NC_000015.9:g.44890991A>G , CM000677.1:g.44890991A>G GRCh37
NC_000015.8:g.42678283A>G NCBI36
NG_008885.1:g.69886T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.3730T>C ENSP00000453246.2:p.Ser1244Pro
ENST00000682065.1:c.3730T>C ENSP00000507025.1:p.Ser1244Pro
ENST00000682460.1:c.*150T>C ENSP00000508334.1:n.*150T>C
ENST00000682495.1:c.*222T>C ENSP00000507166.1:n.*222T>C
ENST00000682669.1:c.3529T>C ENSP00000507782.1:p.Ser1177Pro
ENST00000682788.1:c.3730T>C ENSP00000508089.1:p.Ser1244Pro
ENST00000682915.1:c.3823T>C ENSP00000507493.1:n.3823T>C
ENST00000683121.1:c.3730T>C ENSP00000507557.1:p.Ser1244Pro
ENST00000683186.1:c.*493T>C ENSP00000507268.1:n.*493T>C
ENST00000683496.1:c.3730T>C ENSP00000506968.1:p.Ser1244Pro
ENST00000683734.1:c.3730T>C ENSP00000508319.1:p.Ser1244Pro
ENST00000683753.1:n.2776T>C
ENST00000683838.1:n.804T>C
ENST00000684038.1:c.*150T>C ENSP00000507141.1:n.*150T>C
ENST00000684235.1:c.3730T>C ENSP00000508295.1:p.Ser1244Pro
ENST00000684676.1:c.3730T>C ENSP00000506948.1:p.Ser1244Pro
ENST00000261866.12:c.3730T>C MANE Select ENSP00000261866.7:p.Ser1244Pro
ENST00000261866.11:c.3730T>C ENSP00000261866.7:p.Ser1244Pro
ENST00000427534.6:c.3730T>C ENSP00000396110.2:p.Ser1244Pro
ENST00000535302.6:c.3730T>C ENSP00000445278.2:p.Ser1244Pro
ENST00000558093.1:n.344T>C
ENST00000558319.5:c.3730T>C ENSP00000453599.1:p.Ser1244Pro
NM_001160227.1:c.3730T>C NP_001153699.1:p.Ser1244Pro
NM_025137.3:c.3730T>C NP_079413.3:p.Ser1244Pro
XM_005254695.3:c.3472T>C XP_005254752.1:p.Ser1158Pro
XM_006720700.1:c.3730T>C XP_006720763.1:p.Ser1244Pro
XM_006720701.2:c.3730T>C XP_006720764.1:p.Ser1244Pro
XM_011522093.1:c.3687-420T>C XP_011520395.1:n.3687-420T>C
XR_931917.1:n.3761T>C
XM_006720701.3:c.3730T>C XP_006720764.1:p.Ser1244Pro
XM_017022634.1:c.3730T>C XP_016878123.1:p.Ser1244Pro
XM_017022635.2:c.3730T>C XP_016878124.1:p.Ser1244Pro
XM_017022636.1:c.607T>C XP_016878125.1:p.Ser203Pro
XR_001751402.1:n.3718-420T>C
XR_931917.2:n.3761T>C
NM_025137.4:c.3730T>C MANE Select NP_079413.3:p.Ser1244Pro
NM_001160227.2:c.3730T>C NP_001153699.1:p.Ser1244Pro