Canonical Allele Identifier: CA7534391

Gene: SPG11

Linked Data

• dbSNP Id: rs772425559
• ExAC: 15:44876339 C / A
• gnomAD v2: 15-44876339-C-A
• gnomAD v4: 15-44584141-C-A
• MyVariant Identifiers: chr15:g.44876339C>A (hg19) ; chr15:g.44584141C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584141C>A , CM000677.2:g.44584141C>A	GRCh38
NC_000015.9:g.44876339C>A , CM000677.1:g.44876339C>A	GRCh37
NC_000015.8:g.42663631C>A	NCBI36
NG_008885.1:g.84538G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5539G>T	ENSP00000453246.2:p.Ala1847Ser
ENST00000561391.2:n.1767G>T
ENST00000682065.1:c.5395G>T	ENSP00000507025.1:p.Ala1799Ser
ENST00000682460.1:c.*1796G>T	ENSP00000508334.1:n.*1796G>T
ENST00000682495.1:c.*2031G>T	ENSP00000507166.1:n.*2031G>T
ENST00000682669.1:c.5338G>T	ENSP00000507782.1:p.Ala1780Ser
ENST00000683186.1:c.*2302G>T	ENSP00000507268.1:n.*2302G>T
ENST00000683496.1:c.5539G>T	ENSP00000506968.1:p.Ala1847Ser
ENST00000683734.1:c.5539G>T	ENSP00000508319.1:p.Ala1847Ser
ENST00000683753.1:n.4585G>T
ENST00000684038.1:c.*1959G>T	ENSP00000507141.1:n.*1959G>T
ENST00000684235.1:c.5539G>T	ENSP00000508295.1:p.Ala1847Ser
ENST00000684676.1:c.5515+24G>T	ENSP00000506948.1:n.5515+24G>T
ENST00000261866.12:c.5539G>T MANE Select	ENSP00000261866.7:p.Ala1847Ser
ENST00000261866.11:c.5539G>T	ENSP00000261866.7:p.Ala1847Ser
ENST00000427534.6:c.5539G>T	ENSP00000396110.2:p.Ala1847Ser
ENST00000535302.6:c.5539G>T	ENSP00000445278.2:p.Ala1847Ser
ENST00000558319.5:c.5539G>T	ENSP00000453599.1:p.Ala1847Ser
ENST00000559511.5:c.387G>T
ENST00000559822.1:c.287+24G>T
NM_001160227.1:c.5539G>T	NP_001153699.1:p.Ala1847Ser
NM_025137.3:c.5539G>T	NP_079413.3:p.Ala1847Ser
XM_005254695.3:c.5281G>T	XP_005254752.1:p.Ala1761Ser
XM_006720700.1:c.5395G>T	XP_006720763.1:p.Ala1799Ser
XM_017022634.1:c.5539G>T	XP_016878123.1:p.Ala1847Ser
XM_017022636.1:c.2416G>T	XP_016878125.1:p.Ala806Ser
NM_025137.4:c.5539G>T MANE Select	NP_079413.3:p.Ala1847Ser
NM_001160227.2:c.5539G>T	NP_001153699.1:p.Ala1847Ser