Canonical Allele Identifier: CA490329876

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44876441T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584243T>G , CM000677.2:g.44584243T>G	GRCh38
NC_000015.9:g.44876441T>G , CM000677.1:g.44876441T>G	GRCh37
NC_000015.8:g.42663733T>G	NCBI36
NG_008885.1:g.84436A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5437A>C	ENSP00000453246.2:p.Arg1813=
ENST00000561391.2:n.1665A>C
ENST00000682065.1:c.5293A>C	ENSP00000507025.1:p.Arg1765=
ENST00000682460.1:c.*1694A>C	ENSP00000508334.1:n.*1694A>C
ENST00000682495.1:c.*1929A>C	ENSP00000507166.1:n.*1929A>C
ENST00000682669.1:c.5236A>C	ENSP00000507782.1:p.Arg1746=
ENST00000683186.1:c.*2200A>C	ENSP00000507268.1:n.*2200A>C
ENST00000683496.1:c.5437A>C	ENSP00000506968.1:p.Arg1813=
ENST00000683734.1:c.5437A>C	ENSP00000508319.1:p.Arg1813=
ENST00000683753.1:n.4483A>C
ENST00000684038.1:c.*1857A>C	ENSP00000507141.1:n.*1857A>C
ENST00000684235.1:c.5437A>C	ENSP00000508295.1:p.Arg1813=
ENST00000684676.1:c.5437A>C	ENSP00000506948.1:p.Arg1813=
ENST00000261866.12:c.5437A>C MANE Select	ENSP00000261866.7:p.Arg1813=
ENST00000261866.11:c.5437A>C	ENSP00000261866.7:p.Arg1813=
ENST00000427534.6:c.5437A>C	ENSP00000396110.2:p.Arg1813=
ENST00000535302.6:c.5437A>C	ENSP00000445278.2:p.Arg1813=
ENST00000558319.5:c.5437A>C	ENSP00000453599.1:p.Arg1813=
ENST00000559511.5:c.285A>C
ENST00000559822.1:c.209A>C
NM_001160227.1:c.5437A>C	NP_001153699.1:p.Arg1813=
NM_025137.3:c.5437A>C	NP_079413.3:p.Arg1813=
XM_005254695.3:c.5179A>C	XP_005254752.1:p.Arg1727=
XM_006720700.1:c.5293A>C	XP_006720763.1:p.Arg1765=
XM_017022634.1:c.5437A>C	XP_016878123.1:p.Arg1813=
XM_017022636.1:c.2314A>C	XP_016878125.1:p.Arg772=
NM_025137.4:c.5437A>C MANE Select	NP_079413.3:p.Arg1813=
NM_001160227.2:c.5437A>C	NP_001153699.1:p.Arg1813=