Canonical Allele Identifier: CA2173694807

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584057G= , CM000677.2:g.44584057G=	GRCh38
NC_000015.9:g.44876255G= , CM000677.1:g.44876255G=	GRCh37
NC_000015.8:g.42663547G=	NCBI36
NG_008885.1:g.84622C=

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.5623C= MANE Select	NP_079413.3:p.Gln1875=
ENST00000261866.12:c.5623C= MANE Select	ENSP00000261866.7:p.Gln1875=
NM_001160227.1:c.5623C=	NP_001153699.1:p.Gln1875=
NM_001160227.2:c.5623C=	NP_001153699.1:p.Gln1875=
NM_025137.3:c.5623C=	NP_079413.3:p.Gln1875=
ENST00000261866.11:c.5623C=	ENSP00000261866.7:p.Gln1875=
ENST00000427534.6:c.5623C=	ENSP00000396110.2:p.Gln1875=
ENST00000535302.6:c.5623C=	ENSP00000445278.2:p.Gln1875=
ENST00000558319.5:c.5623C=	ENSP00000453599.1:p.Gln1875=
ENST00000559511.5:c.471C=
ENST00000559511.6:c.5623C=	ENSP00000453246.2:p.Gln1875=
ENST00000559822.1:c.287+108C=
ENST00000561391.2:n.1851C=
ENST00000682065.1:c.5479C=	ENSP00000507025.1:p.Gln1827=
ENST00000682460.1:c.*1880C=	ENSP00000508334.1:n.*1880C=
ENST00000682495.1:c.*2115C=	ENSP00000507166.1:n.*2115C=
ENST00000682669.1:c.5422C=	ENSP00000507782.1:p.Gln1808=
ENST00000683186.1:c.*2386C=	ENSP00000507268.1:n.*2386C=
ENST00000683496.1:c.5623C=	ENSP00000506968.1:p.Gln1875=
ENST00000683734.1:c.5623C=	ENSP00000508319.1:p.Gln1875=
ENST00000683753.1:n.4669C=
ENST00000684038.1:c.*2043C=	ENSP00000507141.1:n.*2043C=
ENST00000684235.1:c.5623C=	ENSP00000508295.1:p.Gln1875=
ENST00000684676.1:c.5515+108C=	ENSP00000506948.1:n.5515+108C=
XM_005254695.3:c.5365C=	XP_005254752.1:p.Gln1789=
XM_006720700.1:c.5479C=	XP_006720763.1:p.Gln1827=
XM_017022634.1:c.5623C=	XP_016878123.1:p.Gln1875=
XM_017022636.1:c.2500C=	XP_016878125.1:p.Gln834=