Canonical Allele Identifier: CA392222920

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44876611G>A (hg19) ; chr15:g.44584413G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584413G>A , CM000677.2:g.44584413G>A	GRCh38
NC_000015.9:g.44876611G>A , CM000677.1:g.44876611G>A	GRCh37
NC_000015.8:g.42663903G>A	NCBI36
NG_008885.1:g.84266C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5267C>T	ENSP00000453246.2:p.Ala1756Val
ENST00000561391.2:n.1495C>T
ENST00000682065.1:c.5123C>T	ENSP00000507025.1:p.Ala1708Val
ENST00000682460.1:c.*1524C>T	ENSP00000508334.1:n.*1524C>T
ENST00000682495.1:c.*1759C>T	ENSP00000507166.1:n.*1759C>T
ENST00000682669.1:c.5066C>T	ENSP00000507782.1:p.Ala1689Val
ENST00000683186.1:c.*2030C>T	ENSP00000507268.1:n.*2030C>T
ENST00000683496.1:c.5267C>T	ENSP00000506968.1:p.Ala1756Val
ENST00000683734.1:c.5267C>T	ENSP00000508319.1:p.Ala1756Val
ENST00000683753.1:n.4313C>T
ENST00000684038.1:c.*1687C>T	ENSP00000507141.1:n.*1687C>T
ENST00000684235.1:c.5267C>T	ENSP00000508295.1:p.Ala1756Val
ENST00000684676.1:c.5267C>T	ENSP00000506948.1:p.Ala1756Val
ENST00000261866.12:c.5267C>T MANE Select	ENSP00000261866.7:p.Ala1756Val
ENST00000261866.11:c.5267C>T	ENSP00000261866.7:p.Ala1756Val
ENST00000427534.6:c.5267C>T	ENSP00000396110.2:p.Ala1756Val
ENST00000535302.6:c.5267C>T	ENSP00000445278.2:p.Ala1756Val
ENST00000558319.5:c.5267C>T	ENSP00000453599.1:p.Ala1756Val
ENST00000558790.5:n.704C>T
ENST00000559511.5:c.115C>T
ENST00000559822.1:c.39C>T
NM_001160227.1:c.5267C>T	NP_001153699.1:p.Ala1756Val
NM_025137.3:c.5267C>T	NP_079413.3:p.Ala1756Val
XM_005254695.3:c.5009C>T	XP_005254752.1:p.Ala1670Val
XM_006720700.1:c.5123C>T	XP_006720763.1:p.Ala1708Val
XM_017022634.1:c.5267C>T	XP_016878123.1:p.Ala1756Val
XM_017022636.1:c.2144C>T	XP_016878125.1:p.Ala715Val
XR_931917.2:n.5321C>T
NM_025137.4:c.5267C>T MANE Select	NP_079413.3:p.Ala1756Val
NM_001160227.2:c.5267C>T	NP_001153699.1:p.Ala1756Val