Canonical Allele Identifier: CA392218124

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44865762G>A (hg19) ; chr15:g.44573564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44573564G>A , CM000677.2:g.44573564G>A	GRCh38
NC_000015.9:g.44865762G>A , CM000677.1:g.44865762G>A	GRCh37
NC_000015.8:g.42653054G>A	NCBI36
NG_008885.1:g.95115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-2906C>T	ENSP00000453246.2:n.5867-2906C>T
ENST00000561391.2:n.2416C>T
ENST00000682065.1:c.6044C>T	ENSP00000507025.1:p.Thr2015Ile
ENST00000682460.1:c.*2445C>T	ENSP00000508334.1:n.*2445C>T
ENST00000682495.1:c.*2680C>T	ENSP00000507166.1:n.*2680C>T
ENST00000682669.1:c.5987C>T	ENSP00000507782.1:p.Thr1996Ile
ENST00000683186.1:c.*2951C>T	ENSP00000507268.1:n.*2951C>T
ENST00000683496.1:c.6006+1338C>T	ENSP00000506968.1:n.6006+1338C>T
ENST00000683734.1:c.*138C>T	ENSP00000508319.1:n.*138C>T
ENST00000683753.1:n.5234C>T
ENST00000684038.1:c.*2608C>T	ENSP00000507141.1:n.*2608C>T
ENST00000684235.1:c.6188C>T	ENSP00000508295.1:p.Thr2063Ile
ENST00000684676.1:c.*337C>T	ENSP00000506948.1:n.*337C>T
ENST00000261866.12:c.6188C>T MANE Select	ENSP00000261866.7:p.Thr2063Ile
ENST00000261866.11:c.6188C>T	ENSP00000261866.7:p.Thr2063Ile
ENST00000427534.6:c.6188C>T	ENSP00000396110.2:p.Thr2063Ile
ENST00000535302.6:c.5867-744C>T	ENSP00000445278.2:n.5867-744C>T
ENST00000558080.1:n.553C>T
ENST00000558319.5:c.6188C>T	ENSP00000453599.1:p.Thr2063Ile
ENST00000559511.5:c.715-2906C>T
ENST00000559933.1:n.257C>T
ENST00000561268.5:n.120C>T
NM_001160227.1:c.5867-744C>T	NP_001153699.1:n.5867-744C>T
NM_025137.3:c.6188C>T	NP_079413.3:p.Thr2063Ile
XM_005254695.3:c.5930C>T	XP_005254752.1:p.Thr1977Ile
XM_006720700.1:c.6044C>T	XP_006720763.1:p.Thr2015Ile
XM_017022634.1:c.6188C>T	XP_016878123.1:p.Thr2063Ile
XM_017022636.1:c.3065C>T	XP_016878125.1:p.Thr1022Ile
NM_025137.4:c.6188C>T MANE Select	NP_079413.3:p.Thr2063Ile
NM_001160227.2:c.5867-744C>T	NP_001153699.1:n.5867-744C>T