Canonical Allele Identifier: CA2628200881

Gene: SPG11

Linked Data

• gnomAD v4: 15-44570456-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44570456G>T , CM000677.2:g.44570456G>T	GRCh38
NC_000015.9:g.44862654G>T , CM000677.1:g.44862654G>T	GRCh37
NC_000015.8:g.42649946G>T	NCBI36
NG_008885.1:g.98223C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558138.2:c.276+69C>A	ENSP00000453314.2:n.276+69C>A
ENST00000559511.6:c.6000+69C>A	ENSP00000453246.2:n.6000+69C>A
ENST00000682065.1:c.6333+69C>A	ENSP00000507025.1:n.6333+69C>A
ENST00000682460.1:c.*2734+69C>A	ENSP00000508334.1:n.*2734+69C>A
ENST00000682495.1:c.*2969+69C>A	ENSP00000507166.1:n.*2969+69C>A
ENST00000682669.1:c.6276+69C>A	ENSP00000507782.1:n.6276+69C>A
ENST00000683186.1:c.*3240+69C>A	ENSP00000507268.1:n.*3240+69C>A
ENST00000683496.1:c.*119+69C>A	ENSP00000506968.1:n.*119+69C>A
ENST00000683734.1:c.*427+69C>A	ENSP00000508319.1:n.*427+69C>A
ENST00000683753.1:n.5523+69C>A
ENST00000684038.1:c.*2897+69C>A	ENSP00000507141.1:n.*2897+69C>A
ENST00000684235.1:c.6477+69C>A	ENSP00000508295.1:n.6477+69C>A
ENST00000261866.12:c.6477+69C>A MANE Select	ENSP00000261866.7:n.6477+69C>A
ENST00000261866.11:c.6477+69C>A	ENSP00000261866.7:n.6477+69C>A
ENST00000427534.6:c.6477+69C>A	ENSP00000396110.2:n.6477+69C>A
ENST00000535302.6:c.6138+69C>A	ENSP00000445278.2:n.6138+69C>A
ENST00000558138.1:c.276+69C>A	ENSP00000453314.1:n.276+69C>A
ENST00000559347.1:n.306+69C>A
ENST00000559511.5:c.848+69C>A
ENST00000561268.5:n.275+2227C>A
NM_001160227.1:c.6138+69C>A	NP_001153699.1:n.6138+69C>A
NM_025137.3:c.6477+69C>A	NP_079413.3:n.6477+69C>A
XM_005254695.3:c.6219+69C>A	XP_005254752.1:n.6219+69C>A
XM_006720700.1:c.6333+69C>A	XP_006720763.1:n.6333+69C>A
XM_017022634.1:c.6477+69C>A	XP_016878123.1:n.6477+69C>A
XM_017022636.1:c.3354+69C>A	XP_016878125.1:n.3354+69C>A
NM_025137.4:c.6477+69C>A MANE Select	NP_079413.3:n.6477+69C>A
NM_001160227.2:c.6138+69C>A	NP_001153699.1:n.6138+69C>A