Canonical Allele Identifier: CA392216288

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44862752G>T (hg19) ; chr15:g.44570554G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44570554G>T , CM000677.2:g.44570554G>T	GRCh38
NC_000015.9:g.44862752G>T , CM000677.1:g.44862752G>T	GRCh37
NC_000015.8:g.42650044G>T	NCBI36
NG_008885.1:g.98125C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558138.2:c.247C>A	ENSP00000453314.2:p.Leu83Met
ENST00000559511.6:c.5971C>A	ENSP00000453246.2:p.Leu1991Met
ENST00000682065.1:c.6304C>A	ENSP00000507025.1:p.Leu2102Met
ENST00000682460.1:c.*2705C>A	ENSP00000508334.1:n.*2705C>A
ENST00000682495.1:c.*2940C>A	ENSP00000507166.1:n.*2940C>A
ENST00000682669.1:c.6247C>A	ENSP00000507782.1:p.Leu2083Met
ENST00000683186.1:c.*3211C>A	ENSP00000507268.1:n.*3211C>A
ENST00000683496.1:c.*90C>A	ENSP00000506968.1:n.*90C>A
ENST00000683734.1:c.*398C>A	ENSP00000508319.1:n.*398C>A
ENST00000683753.1:n.5494C>A
ENST00000684038.1:c.*2868C>A	ENSP00000507141.1:n.*2868C>A
ENST00000684235.1:c.6448C>A	ENSP00000508295.1:p.Leu2150Met
ENST00000261866.12:c.6448C>A MANE Select	ENSP00000261866.7:p.Leu2150Met
ENST00000261866.11:c.6448C>A	ENSP00000261866.7:p.Leu2150Met
ENST00000427534.6:c.6448C>A	ENSP00000396110.2:p.Leu2150Met
ENST00000535302.6:c.6109C>A	ENSP00000445278.2:p.Leu2037Met
ENST00000558138.1:c.247C>A	ENSP00000453314.1:p.Leu83Met
ENST00000559347.1:n.277C>A
ENST00000559511.5:c.819C>A
ENST00000559933.1:n.517C>A
ENST00000561268.5:n.275+2129C>A
NM_001160227.1:c.6109C>A	NP_001153699.1:p.Leu2037Met
NM_025137.3:c.6448C>A	NP_079413.3:p.Leu2150Met
XM_005254695.3:c.6190C>A	XP_005254752.1:p.Leu2064Met
XM_006720700.1:c.6304C>A	XP_006720763.1:p.Leu2102Met
XM_017022634.1:c.6448C>A	XP_016878123.1:p.Leu2150Met
XM_017022636.1:c.3325C>A	XP_016878125.1:p.Leu1109Met
NM_025137.4:c.6448C>A MANE Select	NP_079413.3:p.Leu2150Met
NM_001160227.2:c.6109C>A	NP_001153699.1:p.Leu2037Met