Canonical Allele Identifier: CA490329741

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44876736G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584538G>T , CM000677.2:g.44584538G>T	GRCh38
NC_000015.9:g.44876736G>T , CM000677.1:g.44876736G>T	GRCh37
NC_000015.8:g.42664028G>T	NCBI36
NG_008885.1:g.84141C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5142C>A	ENSP00000453246.2:p.Thr1714=
ENST00000561391.2:n.1370C>A
ENST00000682065.1:c.5122-124C>A	ENSP00000507025.1:n.5122-124C>A
ENST00000682460.1:c.*1399C>A	ENSP00000508334.1:n.*1399C>A
ENST00000682495.1:c.*1634C>A	ENSP00000507166.1:n.*1634C>A
ENST00000682669.1:c.4941C>A	ENSP00000507782.1:p.Thr1647=
ENST00000683186.1:c.*1905C>A	ENSP00000507268.1:n.*1905C>A
ENST00000683496.1:c.5142C>A	ENSP00000506968.1:p.Thr1714=
ENST00000683734.1:c.5142C>A	ENSP00000508319.1:p.Thr1714=
ENST00000683753.1:n.4188C>A
ENST00000684038.1:c.*1562C>A	ENSP00000507141.1:n.*1562C>A
ENST00000684235.1:c.5142C>A	ENSP00000508295.1:p.Thr1714=
ENST00000684676.1:c.5142C>A	ENSP00000506948.1:p.Thr1714=
ENST00000261866.12:c.5142C>A MANE Select	ENSP00000261866.7:p.Thr1714=
ENST00000261866.11:c.5142C>A	ENSP00000261866.7:p.Thr1714=
ENST00000427534.6:c.5142C>A	ENSP00000396110.2:p.Thr1714=
ENST00000535302.6:c.5142C>A	ENSP00000445278.2:p.Thr1714=
ENST00000558319.5:c.5142C>A	ENSP00000453599.1:p.Thr1714=
ENST00000558790.5:n.579C>A
NM_001160227.1:c.5142C>A	NP_001153699.1:p.Thr1714=
NM_025137.3:c.5142C>A	NP_079413.3:p.Thr1714=
XM_005254695.3:c.4884C>A	XP_005254752.1:p.Thr1628=
XM_006720700.1:c.5122-124C>A	XP_006720763.1:n.5122-124C>A
XM_017022634.1:c.5142C>A	XP_016878123.1:p.Thr1714=
XM_017022636.1:c.2019C>A	XP_016878125.1:p.Thr673=
XR_931917.2:n.5196C>A
NM_025137.4:c.5142C>A MANE Select	NP_079413.3:p.Thr1714=
NM_001160227.2:c.5142C>A	NP_001153699.1:p.Thr1714=