Canonical Allele Identifier: CA490207803

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44890923G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598725G>A , CM000677.2:g.44598725G>A	GRCh38
NC_000015.9:g.44890923G>A , CM000677.1:g.44890923G>A	GRCh37
NC_000015.8:g.42678215G>A	NCBI36
NG_008885.1:g.69954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3798C>T	ENSP00000453246.2:p.Leu1266=
ENST00000682065.1:c.3798C>T	ENSP00000507025.1:p.Leu1266=
ENST00000682460.1:c.*218C>T	ENSP00000508334.1:n.*218C>T
ENST00000682495.1:c.*290C>T	ENSP00000507166.1:n.*290C>T
ENST00000682669.1:c.3597C>T	ENSP00000507782.1:p.Leu1199=
ENST00000682788.1:c.3798C>T	ENSP00000508089.1:p.Leu1266=
ENST00000682915.1:c.3891C>T	ENSP00000507493.1:n.3891C>T
ENST00000683121.1:c.3798C>T	ENSP00000507557.1:p.Leu1266=
ENST00000683186.1:c.*561C>T	ENSP00000507268.1:n.*561C>T
ENST00000683496.1:c.3798C>T	ENSP00000506968.1:p.Leu1266=
ENST00000683734.1:c.3798C>T	ENSP00000508319.1:p.Leu1266=
ENST00000683753.1:n.2844C>T
ENST00000683838.1:n.872C>T
ENST00000684038.1:c.*218C>T	ENSP00000507141.1:n.*218C>T
ENST00000684235.1:c.3798C>T	ENSP00000508295.1:p.Leu1266=
ENST00000684676.1:c.3798C>T	ENSP00000506948.1:p.Leu1266=
ENST00000261866.12:c.3798C>T MANE Select	ENSP00000261866.7:p.Leu1266=
ENST00000261866.11:c.3798C>T	ENSP00000261866.7:p.Leu1266=
ENST00000427534.6:c.3798C>T	ENSP00000396110.2:p.Leu1266=
ENST00000535302.6:c.3798C>T	ENSP00000445278.2:p.Leu1266=
ENST00000558093.1:n.412C>T
ENST00000558319.5:c.3798C>T	ENSP00000453599.1:p.Leu1266=
NM_001160227.1:c.3798C>T	NP_001153699.1:p.Leu1266=
NM_025137.3:c.3798C>T	NP_079413.3:p.Leu1266=
XM_005254695.3:c.3540C>T	XP_005254752.1:p.Leu1180=
XM_006720700.1:c.3798C>T	XP_006720763.1:p.Leu1266=
XM_006720701.2:c.3798C>T	XP_006720764.1:p.Leu1266=
XM_011522093.1:c.3687-352C>T	XP_011520395.1:n.3687-352C>T
XR_931917.1:n.3829C>T
XM_006720701.3:c.3798C>T	XP_006720764.1:p.Leu1266=
XM_017022634.1:c.3798C>T	XP_016878123.1:p.Leu1266=
XM_017022635.2:c.3798C>T	XP_016878124.1:p.Leu1266=
XM_017022636.1:c.675C>T	XP_016878125.1:p.Leu225=
XR_001751402.1:n.3718-352C>T
XR_931917.2:n.3829C>T
NM_025137.4:c.3798C>T MANE Select	NP_079413.3:p.Leu1266=
NM_001160227.2:c.3798C>T	NP_001153699.1:p.Leu1266=