Canonical Allele Identifier: CA490203533

Gene: SPG11

Linked Data

• ClinVar Variation Id: 2719808
• ClinVar RCV Id: RCV003496916
• gnomAD v4: 15-44574926-G-A
• MyVariant Identifiers: chr15:g.44867124G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44574926G>A , CM000677.2:g.44574926G>A	GRCh38
NC_000015.9:g.44867124G>A , CM000677.1:g.44867124G>A	GRCh37
NC_000015.8:g.42654416G>A	NCBI36
NG_008885.1:g.93753C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4268C>T	ENSP00000453246.2:n.5867-4268C>T
ENST00000561391.2:n.2210C>T
ENST00000682065.1:c.5838C>T	ENSP00000507025.1:p.Val1946=
ENST00000682460.1:c.*2239C>T	ENSP00000508334.1:n.*2239C>T
ENST00000682495.1:c.*2474C>T	ENSP00000507166.1:n.*2474C>T
ENST00000682669.1:c.5781C>T	ENSP00000507782.1:p.Val1927=
ENST00000683186.1:c.*2745C>T	ENSP00000507268.1:n.*2745C>T
ENST00000683496.1:c.5982C>T	ENSP00000506968.1:p.Val1994=
ENST00000683734.1:c.5867-1181C>T	ENSP00000508319.1:n.5867-1181C>T
ENST00000683753.1:n.5028C>T
ENST00000684038.1:c.*2402C>T	ENSP00000507141.1:n.*2402C>T
ENST00000684235.1:c.5982C>T	ENSP00000508295.1:p.Val1994=
ENST00000684676.1:c.*131C>T	ENSP00000506948.1:n.*131C>T
ENST00000261866.12:c.5982C>T MANE Select	ENSP00000261866.7:p.Val1994=
ENST00000261866.11:c.5982C>T	ENSP00000261866.7:p.Val1994=
ENST00000427534.6:c.5982C>T	ENSP00000396110.2:p.Val1994=
ENST00000535302.6:c.5867-2106C>T	ENSP00000445278.2:n.5867-2106C>T
ENST00000558080.1:n.347C>T
ENST00000558319.5:c.5982C>T	ENSP00000453599.1:p.Val1994=
ENST00000559511.5:c.715-4268C>T
ENST00000559822.1:c.525C>T
NM_001160227.1:c.5867-2106C>T	NP_001153699.1:n.5867-2106C>T
NM_025137.3:c.5982C>T	NP_079413.3:p.Val1994=
XM_005254695.3:c.5724C>T	XP_005254752.1:p.Val1908=
XM_006720700.1:c.5838C>T	XP_006720763.1:p.Val1946=
XM_017022634.1:c.5982C>T	XP_016878123.1:p.Val1994=
XM_017022636.1:c.2859C>T	XP_016878125.1:p.Val953=
NM_025137.4:c.5982C>T MANE Select	NP_079413.3:p.Val1994=
NM_001160227.2:c.5867-2106C>T	NP_001153699.1:n.5867-2106C>T