Canonical Allele Identifier: CA490203405

Gene: SPG11

Linked Data

• gnomAD v4: 15-44572725-A-G
• MyVariant Identifiers: chr15:g.44864923A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44572725A>G , CM000677.2:g.44572725A>G	GRCh38
NC_000015.9:g.44864923A>G , CM000677.1:g.44864923A>G	GRCh37
NC_000015.8:g.42652215A>G	NCBI36
NG_008885.1:g.95954T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000558138.2:c.100T>C	ENSP00000453314.2:p.Leu34=
ENST00000559511.6:c.5867-2067T>C	ENSP00000453246.2:n.5867-2067T>C
ENST00000682065.1:c.6157T>C	ENSP00000507025.1:p.Leu2053=
ENST00000682460.1:c.*2558T>C	ENSP00000508334.1:n.*2558T>C
ENST00000682495.1:c.*2793T>C	ENSP00000507166.1:n.*2793T>C
ENST00000682669.1:c.6100T>C	ENSP00000507782.1:p.Leu2034=
ENST00000683186.1:c.*3064T>C	ENSP00000507268.1:n.*3064T>C
ENST00000683496.1:c.6007-2073T>C	ENSP00000506968.1:n.6007-2073T>C
ENST00000683734.1:c.*251T>C	ENSP00000508319.1:n.*251T>C
ENST00000683753.1:n.5347T>C
ENST00000684038.1:c.*2721T>C	ENSP00000507141.1:n.*2721T>C
ENST00000684235.1:c.6301T>C	ENSP00000508295.1:p.Leu2101=
ENST00000261866.12:c.6301T>C MANE Select	ENSP00000261866.7:p.Leu2101=
ENST00000261866.11:c.6301T>C	ENSP00000261866.7:p.Leu2101=
ENST00000427534.6:c.6301T>C	ENSP00000396110.2:p.Leu2101=
ENST00000535302.6:c.5962T>C	ENSP00000445278.2:p.Leu1988=
ENST00000558138.1:c.100T>C	ENSP00000453314.1:p.Leu34=
ENST00000559511.5:c.715-2067T>C
ENST00000559933.1:n.370T>C
ENST00000561268.5:n.233T>C
NM_001160227.1:c.5962T>C	NP_001153699.1:p.Leu1988=
NM_025137.3:c.6301T>C	NP_079413.3:p.Leu2101=
XM_005254695.3:c.6043T>C	XP_005254752.1:p.Leu2015=
XM_006720700.1:c.6157T>C	XP_006720763.1:p.Leu2053=
XM_017022634.1:c.6301T>C	XP_016878123.1:p.Leu2101=
XM_017022636.1:c.3178T>C	XP_016878125.1:p.Leu1060=
NM_025137.4:c.6301T>C MANE Select	NP_079413.3:p.Leu2101=
NM_001160227.2:c.5962T>C	NP_001153699.1:p.Leu1988=