Canonical Allele Identifier: CA392230352

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44890985G>C (hg19) ; chr15:g.44598787G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598787G>C , CM000677.2:g.44598787G>C	GRCh38
NC_000015.9:g.44890985G>C , CM000677.1:g.44890985G>C	GRCh37
NC_000015.8:g.42678277G>C	NCBI36
NG_008885.1:g.69892C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3736C>G	ENSP00000453246.2:p.His1246Asp
ENST00000682065.1:c.3736C>G	ENSP00000507025.1:p.His1246Asp
ENST00000682460.1:c.*156C>G	ENSP00000508334.1:n.*156C>G
ENST00000682495.1:c.*228C>G	ENSP00000507166.1:n.*228C>G
ENST00000682669.1:c.3535C>G	ENSP00000507782.1:p.His1179Asp
ENST00000682788.1:c.3736C>G	ENSP00000508089.1:p.His1246Asp
ENST00000682915.1:c.3829C>G	ENSP00000507493.1:n.3829C>G
ENST00000683121.1:c.3736C>G	ENSP00000507557.1:p.His1246Asp
ENST00000683186.1:c.*499C>G	ENSP00000507268.1:n.*499C>G
ENST00000683496.1:c.3736C>G	ENSP00000506968.1:p.His1246Asp
ENST00000683734.1:c.3736C>G	ENSP00000508319.1:p.His1246Asp
ENST00000683753.1:n.2782C>G
ENST00000683838.1:n.810C>G
ENST00000684038.1:c.*156C>G	ENSP00000507141.1:n.*156C>G
ENST00000684235.1:c.3736C>G	ENSP00000508295.1:p.His1246Asp
ENST00000684676.1:c.3736C>G	ENSP00000506948.1:p.His1246Asp
ENST00000261866.12:c.3736C>G MANE Select	ENSP00000261866.7:p.His1246Asp
ENST00000261866.11:c.3736C>G	ENSP00000261866.7:p.His1246Asp
ENST00000427534.6:c.3736C>G	ENSP00000396110.2:p.His1246Asp
ENST00000535302.6:c.3736C>G	ENSP00000445278.2:p.His1246Asp
ENST00000558093.1:n.350C>G
ENST00000558319.5:c.3736C>G	ENSP00000453599.1:p.His1246Asp
NM_001160227.1:c.3736C>G	NP_001153699.1:p.His1246Asp
NM_025137.3:c.3736C>G	NP_079413.3:p.His1246Asp
XM_005254695.3:c.3478C>G	XP_005254752.1:p.His1160Asp
XM_006720700.1:c.3736C>G	XP_006720763.1:p.His1246Asp
XM_006720701.2:c.3736C>G	XP_006720764.1:p.His1246Asp
XM_011522093.1:c.3687-414C>G	XP_011520395.1:n.3687-414C>G
XR_931917.1:n.3767C>G
XM_006720701.3:c.3736C>G	XP_006720764.1:p.His1246Asp
XM_017022634.1:c.3736C>G	XP_016878123.1:p.His1246Asp
XM_017022635.2:c.3736C>G	XP_016878124.1:p.His1246Asp
XM_017022636.1:c.613C>G	XP_016878125.1:p.His205Asp
XR_001751402.1:n.3718-414C>G
XR_931917.2:n.3767C>G
NM_025137.4:c.3736C>G MANE Select	NP_079413.3:p.His1246Asp
NM_001160227.2:c.3736C>G	NP_001153699.1:p.His1246Asp