Canonical Allele Identifier: CA7534437

Gene: SPG11

Linked Data

• ClinVar Variation Id: 2044007
• ClinVar RCV Id: RCV002913428
• dbSNP Id: rs772186328
• ExAC: 15:44876612 C / T
• gnomAD v2: 15-44876612-C-T
• gnomAD v4: 15-44584414-C-T
• MyVariant Identifiers: chr15:g.44876612C>T (hg19) ; chr15:g.44584414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584414C>T , CM000677.2:g.44584414C>T	GRCh38
NC_000015.9:g.44876612C>T , CM000677.1:g.44876612C>T	GRCh37
NC_000015.8:g.42663904C>T	NCBI36
NG_008885.1:g.84265G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5266G>A	ENSP00000453246.2:p.Ala1756Thr
ENST00000561391.2:n.1494G>A
ENST00000682065.1:c.5122G>A	ENSP00000507025.1:p.Ala1708Thr
ENST00000682460.1:c.*1523G>A	ENSP00000508334.1:n.*1523G>A
ENST00000682495.1:c.*1758G>A	ENSP00000507166.1:n.*1758G>A
ENST00000682669.1:c.5065G>A	ENSP00000507782.1:p.Ala1689Thr
ENST00000683186.1:c.*2029G>A	ENSP00000507268.1:n.*2029G>A
ENST00000683496.1:c.5266G>A	ENSP00000506968.1:p.Ala1756Thr
ENST00000683734.1:c.5266G>A	ENSP00000508319.1:p.Ala1756Thr
ENST00000683753.1:n.4312G>A
ENST00000684038.1:c.*1686G>A	ENSP00000507141.1:n.*1686G>A
ENST00000684235.1:c.5266G>A	ENSP00000508295.1:p.Ala1756Thr
ENST00000684676.1:c.5266G>A	ENSP00000506948.1:p.Ala1756Thr
ENST00000261866.12:c.5266G>A MANE Select	ENSP00000261866.7:p.Ala1756Thr
ENST00000261866.11:c.5266G>A	ENSP00000261866.7:p.Ala1756Thr
ENST00000427534.6:c.5266G>A	ENSP00000396110.2:p.Ala1756Thr
ENST00000535302.6:c.5266G>A	ENSP00000445278.2:p.Ala1756Thr
ENST00000558319.5:c.5266G>A	ENSP00000453599.1:p.Ala1756Thr
ENST00000558790.5:n.703G>A
ENST00000559511.5:c.114G>A
ENST00000559822.1:c.38G>A
NM_001160227.1:c.5266G>A	NP_001153699.1:p.Ala1756Thr
NM_025137.3:c.5266G>A	NP_079413.3:p.Ala1756Thr
XM_005254695.3:c.5008G>A	XP_005254752.1:p.Ala1670Thr
XM_006720700.1:c.5122G>A	XP_006720763.1:p.Ala1708Thr
XM_017022634.1:c.5266G>A	XP_016878123.1:p.Ala1756Thr
XM_017022636.1:c.2143G>A	XP_016878125.1:p.Ala715Thr
XR_931917.2:n.5320G>A
NM_025137.4:c.5266G>A MANE Select	NP_079413.3:p.Ala1756Thr
NM_001160227.2:c.5266G>A	NP_001153699.1:p.Ala1756Thr