Canonical Allele Identifier: CA2173685870

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584210G= , CM000677.2:g.44584210G=	GRCh38
NC_000015.9:g.44876408G= , CM000677.1:g.44876408G=	GRCh37
NC_000015.8:g.42663700G=	NCBI36
NG_008885.1:g.84469C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5470C=	ENSP00000453246.2:p.Arg1824=
ENST00000561391.2:n.1698C=
ENST00000682065.1:c.5326C=	ENSP00000507025.1:p.Arg1776=
ENST00000682460.1:c.*1727C=	ENSP00000508334.1:n.*1727C=
ENST00000682495.1:c.*1962C=	ENSP00000507166.1:n.*1962C=
ENST00000682669.1:c.5269C=	ENSP00000507782.1:p.Arg1757=
ENST00000683186.1:c.*2233C=	ENSP00000507268.1:n.*2233C=
ENST00000683496.1:c.5470C=	ENSP00000506968.1:p.Arg1824=
ENST00000683734.1:c.5470C=	ENSP00000508319.1:p.Arg1824=
ENST00000683753.1:n.4516C=
ENST00000684038.1:c.*1890C=	ENSP00000507141.1:n.*1890C=
ENST00000684235.1:c.5470C=	ENSP00000508295.1:p.Arg1824=
ENST00000684676.1:c.5470C=	ENSP00000506948.1:p.Arg1824=
ENST00000261866.12:c.5470C= MANE Select	ENSP00000261866.7:p.Arg1824=
ENST00000261866.11:c.5470C=	ENSP00000261866.7:p.Arg1824=
ENST00000427534.6:c.5470C=	ENSP00000396110.2:p.Arg1824=
ENST00000535302.6:c.5470C=	ENSP00000445278.2:p.Arg1824=
ENST00000558319.5:c.5470C=	ENSP00000453599.1:p.Arg1824=
ENST00000559511.5:c.318C=
ENST00000559822.1:c.242C=
NM_001160227.1:c.5470C=	NP_001153699.1:p.Arg1824=
NM_025137.3:c.5470C=	NP_079413.3:p.Arg1824=
XM_005254695.3:c.5212C=	XP_005254752.1:p.Arg1738=
XM_006720700.1:c.5326C=	XP_006720763.1:p.Arg1776=
XM_017022634.1:c.5470C=	XP_016878123.1:p.Arg1824=
XM_017022636.1:c.2347C=	XP_016878125.1:p.Arg783=
NM_025137.4:c.5470C= MANE Select	NP_079413.3:p.Arg1824=
NM_001160227.2:c.5470C=	NP_001153699.1:p.Arg1824=