Canonical Allele Identifier: CA490203027

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44862726C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44570528C>A , CM000677.2:g.44570528C>A	GRCh38
NC_000015.9:g.44862726C>A , CM000677.1:g.44862726C>A	GRCh37
NC_000015.8:g.42650018C>A	NCBI36
NG_008885.1:g.98151G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000558138.2:c.273G>T	ENSP00000453314.2:p.Leu91=
ENST00000559511.6:c.5997G>T	ENSP00000453246.2:p.Leu1999=
ENST00000682065.1:c.6330G>T	ENSP00000507025.1:p.Leu2110=
ENST00000682460.1:c.*2731G>T	ENSP00000508334.1:n.*2731G>T
ENST00000682495.1:c.*2966G>T	ENSP00000507166.1:n.*2966G>T
ENST00000682669.1:c.6273G>T	ENSP00000507782.1:p.Leu2091=
ENST00000683186.1:c.*3237G>T	ENSP00000507268.1:n.*3237G>T
ENST00000683496.1:c.*116G>T	ENSP00000506968.1:n.*116G>T
ENST00000683734.1:c.*424G>T	ENSP00000508319.1:n.*424G>T
ENST00000683753.1:n.5520G>T
ENST00000684038.1:c.*2894G>T	ENSP00000507141.1:n.*2894G>T
ENST00000684235.1:c.6474G>T	ENSP00000508295.1:p.Leu2158=
ENST00000261866.12:c.6474G>T MANE Select	ENSP00000261866.7:p.Leu2158=
ENST00000261866.11:c.6474G>T	ENSP00000261866.7:p.Leu2158=
ENST00000427534.6:c.6474G>T	ENSP00000396110.2:p.Leu2158=
ENST00000535302.6:c.6135G>T	ENSP00000445278.2:p.Leu2045=
ENST00000558138.1:c.273G>T	ENSP00000453314.1:p.Leu91=
ENST00000559347.1:n.303G>T
ENST00000559511.5:c.845G>T
ENST00000561268.5:n.275+2155G>T
NM_001160227.1:c.6135G>T	NP_001153699.1:p.Leu2045=
NM_025137.3:c.6474G>T	NP_079413.3:p.Leu2158=
XM_005254695.3:c.6216G>T	XP_005254752.1:p.Leu2072=
XM_006720700.1:c.6330G>T	XP_006720763.1:p.Leu2110=
XM_017022634.1:c.6474G>T	XP_016878123.1:p.Leu2158=
XM_017022636.1:c.3351G>T	XP_016878125.1:p.Leu1117=
NM_025137.4:c.6474G>T MANE Select	NP_079413.3:p.Leu2158=
NM_001160227.2:c.6135G>T	NP_001153699.1:p.Leu2045=