Canonical Allele Identifier: CA7534347

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44583884A>G , CM000677.2:g.44583884A>G	GRCh38
NC_000015.9:g.44876082A>G , CM000677.1:g.44876082A>G	GRCh37
NC_000015.8:g.42663374A>G	NCBI36
NG_008885.1:g.84795T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.5796T>C MANE Select	NP_079413.3:p.His1932=
ENST00000261866.12:c.5796T>C MANE Select	ENSP00000261866.7:p.His1932=
NM_001160227.1:c.5796T>C	NP_001153699.1:p.His1932=
NM_001160227.2:c.5796T>C	NP_001153699.1:p.His1932=
NM_025137.3:c.5796T>C	NP_079413.3:p.His1932=
ENST00000261866.11:c.5796T>C	ENSP00000261866.7:p.His1932=
ENST00000427534.6:c.5796T>C	ENSP00000396110.2:p.His1932=
ENST00000535302.6:c.5796T>C	ENSP00000445278.2:p.His1932=
ENST00000558319.5:c.5796T>C	ENSP00000453599.1:p.His1932=
ENST00000559511.5:c.644T>C
ENST00000559511.6:c.5796T>C	ENSP00000453246.2:p.His1932=
ENST00000559822.1:c.339T>C
ENST00000561391.2:n.2024T>C
ENST00000682065.1:c.5652T>C	ENSP00000507025.1:p.His1884=
ENST00000682460.1:c.*2053T>C	ENSP00000508334.1:n.*2053T>C
ENST00000682495.1:c.*2288T>C	ENSP00000507166.1:n.*2288T>C
ENST00000682669.1:c.5595T>C	ENSP00000507782.1:p.His1865=
ENST00000683186.1:c.*2559T>C	ENSP00000507268.1:n.*2559T>C
ENST00000683496.1:c.5796T>C	ENSP00000506968.1:p.His1932=
ENST00000683734.1:c.5796T>C	ENSP00000508319.1:p.His1932=
ENST00000683753.1:n.4842T>C
ENST00000684038.1:c.*2216T>C	ENSP00000507141.1:n.*2216T>C
ENST00000684235.1:c.5796T>C	ENSP00000508295.1:p.His1932=
ENST00000684676.1:c.5567T>C	ENSP00000506948.1:p.Met1856Thr
XM_005254695.3:c.5538T>C	XP_005254752.1:p.His1846=
XM_006720700.1:c.5652T>C	XP_006720763.1:p.His1884=
XM_017022634.1:c.5796T>C	XP_016878123.1:p.His1932=
XM_017022636.1:c.2673T>C	XP_016878125.1:p.His891=