Canonical Allele Identifier: CA2173701357
Gene: SPG11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.44598836C= , CM000677.2:g.44598836C= GRCh38
NC_000015.9:g.44891034C= , CM000677.1:g.44891034C= GRCh37
NC_000015.8:g.42678326C= NCBI36
NG_008885.1:g.69843G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000559511.6:c.3687G= ENSP00000453246.2:p.Leu1229=
ENST00000682065.1:c.3687G= ENSP00000507025.1:p.Leu1229=
ENST00000682460.1:c.*107G= ENSP00000508334.1:n.*107G=
ENST00000682495.1:c.*179G= ENSP00000507166.1:n.*179G=
ENST00000682669.1:c.3486G= ENSP00000507782.1:p.Leu1162=
ENST00000682788.1:c.3687G= ENSP00000508089.1:p.Leu1229=
ENST00000682915.1:c.3780G= ENSP00000507493.1:n.3780G=
ENST00000683121.1:c.3687G= ENSP00000507557.1:p.Leu1229=
ENST00000683186.1:c.*450G= ENSP00000507268.1:n.*450G=
ENST00000683496.1:c.3687G= ENSP00000506968.1:p.Leu1229=
ENST00000683734.1:c.3687G= ENSP00000508319.1:p.Leu1229=
ENST00000683753.1:n.2733G=
ENST00000683838.1:n.761G=
ENST00000684038.1:c.*107G= ENSP00000507141.1:n.*107G=
ENST00000684235.1:c.3687G= ENSP00000508295.1:p.Leu1229=
ENST00000684676.1:c.3687G= ENSP00000506948.1:p.Leu1229=
ENST00000261866.12:c.3687G= MANE Select ENSP00000261866.7:p.Leu1229=
ENST00000261866.11:c.3687G= ENSP00000261866.7:p.Leu1229=
ENST00000427534.6:c.3687G= ENSP00000396110.2:p.Leu1229=
ENST00000535302.6:c.3687G= ENSP00000445278.2:p.Leu1229=
ENST00000558093.1:n.301G=
ENST00000558319.5:c.3687G= ENSP00000453599.1:p.Leu1229=
NM_001160227.1:c.3687G= NP_001153699.1:p.Leu1229=
NM_025137.3:c.3687G= NP_079413.3:p.Leu1229=
XM_005254695.3:c.3429G= XP_005254752.1:p.Leu1143=
XM_006720700.1:c.3687G= XP_006720763.1:p.Leu1229=
XM_006720701.2:c.3687G= XP_006720764.1:p.Leu1229=
XM_011522093.1:c.3687-463G= XP_011520395.1:n.3687-463G=
XR_931917.1:n.3718G=
XM_006720701.3:c.3687G= XP_006720764.1:p.Leu1229=
XM_017022634.1:c.3687G= XP_016878123.1:p.Leu1229=
XM_017022635.2:c.3687G= XP_016878124.1:p.Leu1229=
XM_017022636.1:c.564G= XP_016878125.1:p.Leu188=
XR_001751402.1:n.3718-463G=
XR_931917.2:n.3718G=
NM_025137.4:c.3687G= MANE Select NP_079413.3:p.Leu1229=
NM_001160227.2:c.3687G= NP_001153699.1:p.Leu1229=