Canonical Allele Identifier: CA2173685947

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584236T= , CM000677.2:g.44584236T=	GRCh38
NC_000015.9:g.44876434T= , CM000677.1:g.44876434T=	GRCh37
NC_000015.8:g.42663726T=	NCBI36
NG_008885.1:g.84443A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5444A=	ENSP00000453246.2:p.Gln1815=
ENST00000561391.2:n.1672A=
ENST00000682065.1:c.5300A=	ENSP00000507025.1:p.Gln1767=
ENST00000682460.1:c.*1701A=	ENSP00000508334.1:n.*1701A=
ENST00000682495.1:c.*1936A=	ENSP00000507166.1:n.*1936A=
ENST00000682669.1:c.5243A=	ENSP00000507782.1:p.Gln1748=
ENST00000683186.1:c.*2207A=	ENSP00000507268.1:n.*2207A=
ENST00000683496.1:c.5444A=	ENSP00000506968.1:p.Gln1815=
ENST00000683734.1:c.5444A=	ENSP00000508319.1:p.Gln1815=
ENST00000683753.1:n.4490A=
ENST00000684038.1:c.*1864A=	ENSP00000507141.1:n.*1864A=
ENST00000684235.1:c.5444A=	ENSP00000508295.1:p.Gln1815=
ENST00000684676.1:c.5444A=	ENSP00000506948.1:p.Gln1815=
ENST00000261866.12:c.5444A= MANE Select	ENSP00000261866.7:p.Gln1815=
ENST00000261866.11:c.5444A=	ENSP00000261866.7:p.Gln1815=
ENST00000427534.6:c.5444A=	ENSP00000396110.2:p.Gln1815=
ENST00000535302.6:c.5444A=	ENSP00000445278.2:p.Gln1815=
ENST00000558319.5:c.5444A=	ENSP00000453599.1:p.Gln1815=
ENST00000559511.5:c.292A=
ENST00000559822.1:c.216A=
NM_001160227.1:c.5444A=	NP_001153699.1:p.Gln1815=
NM_025137.3:c.5444A=	NP_079413.3:p.Gln1815=
XM_005254695.3:c.5186A=	XP_005254752.1:p.Gln1729=
XM_006720700.1:c.5300A=	XP_006720763.1:p.Gln1767=
XM_017022634.1:c.5444A=	XP_016878123.1:p.Gln1815=
XM_017022636.1:c.2321A=	XP_016878125.1:p.Gln774=
NM_025137.4:c.5444A= MANE Select	NP_079413.3:p.Gln1815=
NM_001160227.2:c.5444A=	NP_001153699.1:p.Gln1815=