Canonical Allele Identifier: CA392219184

Gene: SPG11

Linked Data

• gnomAD v4: 15-44575028-A-C
• MyVariant Identifiers: chr15:g.44867226A>C (hg19) ; chr15:g.44575028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575028A>C , CM000677.2:g.44575028A>C	GRCh38
NC_000015.9:g.44867226A>C , CM000677.1:g.44867226A>C	GRCh37
NC_000015.8:g.42654518A>C	NCBI36
NG_008885.1:g.93651T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4370T>G	ENSP00000453246.2:n.5867-4370T>G
ENST00000561391.2:n.2108T>G
ENST00000682065.1:c.5736T>G	ENSP00000507025.1:p.Asp1912Glu
ENST00000682460.1:c.*2137T>G	ENSP00000508334.1:n.*2137T>G
ENST00000682495.1:c.*2372T>G	ENSP00000507166.1:n.*2372T>G
ENST00000682669.1:c.5679T>G	ENSP00000507782.1:p.Asp1893Glu
ENST00000683186.1:c.*2643T>G	ENSP00000507268.1:n.*2643T>G
ENST00000683496.1:c.5880T>G	ENSP00000506968.1:p.Asp1960Glu
ENST00000683734.1:c.5867-1283T>G	ENSP00000508319.1:n.5867-1283T>G
ENST00000683753.1:n.4926T>G
ENST00000684038.1:c.*2300T>G	ENSP00000507141.1:n.*2300T>G
ENST00000684235.1:c.5880T>G	ENSP00000508295.1:p.Asp1960Glu
ENST00000684676.1:c.*29T>G	ENSP00000506948.1:n.*29T>G
ENST00000261866.12:c.5880T>G MANE Select	ENSP00000261866.7:p.Asp1960Glu
ENST00000261866.11:c.5880T>G	ENSP00000261866.7:p.Asp1960Glu
ENST00000427534.6:c.5880T>G	ENSP00000396110.2:p.Asp1960Glu
ENST00000535302.6:c.5867-2208T>G	ENSP00000445278.2:n.5867-2208T>G
ENST00000558080.1:n.245T>G
ENST00000558319.5:c.5880T>G	ENSP00000453599.1:p.Asp1960Glu
ENST00000559511.5:c.715-4370T>G
ENST00000559822.1:c.423T>G
NM_001160227.1:c.5867-2208T>G	NP_001153699.1:n.5867-2208T>G
NM_025137.3:c.5880T>G	NP_079413.3:p.Asp1960Glu
XM_005254695.3:c.5622T>G	XP_005254752.1:p.Asp1874Glu
XM_006720700.1:c.5736T>G	XP_006720763.1:p.Asp1912Glu
XM_017022634.1:c.5880T>G	XP_016878123.1:p.Asp1960Glu
XM_017022636.1:c.2757T>G	XP_016878125.1:p.Asp919Glu
NM_025137.4:c.5880T>G MANE Select	NP_079413.3:p.Asp1960Glu
NM_001160227.2:c.5867-2208T>G	NP_001153699.1:n.5867-2208T>G