Canonical Allele Identifier: CA490203540

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44867130T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44574932T>G , CM000677.2:g.44574932T>G	GRCh38
NC_000015.9:g.44867130T>G , CM000677.1:g.44867130T>G	GRCh37
NC_000015.8:g.42654422T>G	NCBI36
NG_008885.1:g.93747A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559511.6:c.5867-4274A>C	ENSP00000453246.2:n.5867-4274A>C
ENST00000561391.2:n.2204A>C
ENST00000682065.1:c.5832A>C	ENSP00000507025.1:p.Arg1944=
ENST00000682460.1:c.*2233A>C	ENSP00000508334.1:n.*2233A>C
ENST00000682495.1:c.*2468A>C	ENSP00000507166.1:n.*2468A>C
ENST00000682669.1:c.5775A>C	ENSP00000507782.1:p.Arg1925=
ENST00000683186.1:c.*2739A>C	ENSP00000507268.1:n.*2739A>C
ENST00000683496.1:c.5976A>C	ENSP00000506968.1:p.Arg1992=
ENST00000683734.1:c.5867-1187A>C	ENSP00000508319.1:n.5867-1187A>C
ENST00000683753.1:n.5022A>C
ENST00000684038.1:c.*2396A>C	ENSP00000507141.1:n.*2396A>C
ENST00000684235.1:c.5976A>C	ENSP00000508295.1:p.Arg1992=
ENST00000684676.1:c.*125A>C	ENSP00000506948.1:n.*125A>C
ENST00000261866.12:c.5976A>C MANE Select	ENSP00000261866.7:p.Arg1992=
ENST00000261866.11:c.5976A>C	ENSP00000261866.7:p.Arg1992=
ENST00000427534.6:c.5976A>C	ENSP00000396110.2:p.Arg1992=
ENST00000535302.6:c.5867-2112A>C	ENSP00000445278.2:n.5867-2112A>C
ENST00000558080.1:n.341A>C
ENST00000558319.5:c.5976A>C	ENSP00000453599.1:p.Arg1992=
ENST00000559511.5:c.715-4274A>C
ENST00000559822.1:c.519A>C
NM_001160227.1:c.5867-2112A>C	NP_001153699.1:n.5867-2112A>C
NM_025137.3:c.5976A>C	NP_079413.3:p.Arg1992=
XM_005254695.3:c.5718A>C	XP_005254752.1:p.Arg1906=
XM_006720700.1:c.5832A>C	XP_006720763.1:p.Arg1944=
XM_017022634.1:c.5976A>C	XP_016878123.1:p.Arg1992=
XM_017022636.1:c.2853A>C	XP_016878125.1:p.Arg951=
NM_025137.4:c.5976A>C MANE Select	NP_079413.3:p.Arg1992=
NM_001160227.2:c.5867-2112A>C	NP_001153699.1:n.5867-2112A>C