Canonical Allele Identifier: CA392221622

Gene: SPG11

Linked Data

• gnomAD v4: 15-44583973-A-C
• MyVariant Identifiers: chr15:g.44876171A>C (hg19) ; chr15:g.44583973A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44583973A>C , CM000677.2:g.44583973A>C	GRCh38
NC_000015.9:g.44876171A>C , CM000677.1:g.44876171A>C	GRCh37
NC_000015.8:g.42663463A>C	NCBI36
NG_008885.1:g.84706T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5707T>G	ENSP00000453246.2:p.Phe1903Val
ENST00000561391.2:n.1935T>G
ENST00000682065.1:c.5563T>G	ENSP00000507025.1:p.Phe1855Val
ENST00000682460.1:c.*1964T>G	ENSP00000508334.1:n.*1964T>G
ENST00000682495.1:c.*2199T>G	ENSP00000507166.1:n.*2199T>G
ENST00000682669.1:c.5506T>G	ENSP00000507782.1:p.Phe1836Val
ENST00000683186.1:c.*2470T>G	ENSP00000507268.1:n.*2470T>G
ENST00000683496.1:c.5707T>G	ENSP00000506968.1:p.Phe1903Val
ENST00000683734.1:c.5707T>G	ENSP00000508319.1:p.Phe1903Val
ENST00000683753.1:n.4753T>G
ENST00000684038.1:c.*2127T>G	ENSP00000507141.1:n.*2127T>G
ENST00000684235.1:c.5707T>G	ENSP00000508295.1:p.Phe1903Val
ENST00000684676.1:c.5516-38T>G	ENSP00000506948.1:n.5516-38T>G
ENST00000261866.12:c.5707T>G MANE Select	ENSP00000261866.7:p.Phe1903Val
ENST00000261866.11:c.5707T>G	ENSP00000261866.7:p.Phe1903Val
ENST00000427534.6:c.5707T>G	ENSP00000396110.2:p.Phe1903Val
ENST00000535302.6:c.5707T>G	ENSP00000445278.2:p.Phe1903Val
ENST00000558319.5:c.5707T>G	ENSP00000453599.1:p.Phe1903Val
ENST00000559511.5:c.555T>G
ENST00000559822.1:c.288-38T>G
NM_001160227.1:c.5707T>G	NP_001153699.1:p.Phe1903Val
NM_025137.3:c.5707T>G	NP_079413.3:p.Phe1903Val
XM_005254695.3:c.5449T>G	XP_005254752.1:p.Phe1817Val
XM_006720700.1:c.5563T>G	XP_006720763.1:p.Phe1855Val
XM_017022634.1:c.5707T>G	XP_016878123.1:p.Phe1903Val
XM_017022636.1:c.2584T>G	XP_016878125.1:p.Phe862Val
NM_025137.4:c.5707T>G MANE Select	NP_079413.3:p.Phe1903Val
NM_001160227.2:c.5707T>G	NP_001153699.1:p.Phe1903Val