Canonical Allele Identifier: CA392231359

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44600626C>G , CM000677.2:g.44600626C>G	GRCh38
NC_000015.9:g.44892824C>G , CM000677.1:g.44892824C>G	GRCh37
NC_000015.8:g.42680116C>G	NCBI36
NG_008885.1:g.68053G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.3527G>C MANE Select	NP_079413.3:p.Trp1176Ser
ENST00000261866.12:c.3527G>C MANE Select	ENSP00000261866.7:p.Trp1176Ser
NM_001160227.1:c.3527G>C	NP_001153699.1:p.Trp1176Ser
NM_001160227.2:c.3527G>C	NP_001153699.1:p.Trp1176Ser
NM_025137.3:c.3527G>C	NP_079413.3:p.Trp1176Ser
ENST00000261866.11:c.3527G>C	ENSP00000261866.7:p.Trp1176Ser
ENST00000427534.6:c.3527G>C	ENSP00000396110.2:p.Trp1176Ser
ENST00000535302.6:c.3527G>C	ENSP00000445278.2:p.Trp1176Ser
ENST00000558093.1:n.141G>C
ENST00000558319.5:c.3527G>C	ENSP00000453599.1:p.Trp1176Ser
ENST00000558988.5:c.254G>C	ENSP00000453921.1:p.Trp85Ser
ENST00000559511.6:c.3527G>C	ENSP00000453246.2:p.Trp1176Ser
ENST00000559754.1:c.349G>C
ENST00000682065.1:c.3527G>C	ENSP00000507025.1:p.Trp1176Ser
ENST00000682460.1:c.3613G>C	ENSP00000508334.1:p.Gly1205Arg
ENST00000682495.1:c.*19G>C	ENSP00000507166.1:n.*19G>C
ENST00000682669.1:c.3454-128G>C	ENSP00000507782.1:n.3454-128G>C
ENST00000682788.1:c.3527G>C	ENSP00000508089.1:p.Trp1176Ser
ENST00000682915.1:c.3620G>C	ENSP00000507493.1:n.3620G>C
ENST00000683121.1:c.3527G>C	ENSP00000507557.1:p.Trp1176Ser
ENST00000683186.1:c.*290G>C	ENSP00000507268.1:n.*290G>C
ENST00000683496.1:c.3527G>C	ENSP00000506968.1:p.Trp1176Ser
ENST00000683734.1:c.3527G>C	ENSP00000508319.1:p.Trp1176Ser
ENST00000683753.1:n.2573G>C
ENST00000683838.1:n.601G>C
ENST00000684038.1:c.3355G>C	ENSP00000507141.1:p.Gly1119Arg
ENST00000684235.1:c.3527G>C	ENSP00000508295.1:p.Trp1176Ser
ENST00000684676.1:c.3527G>C	ENSP00000506948.1:p.Trp1176Ser
XM_005254695.3:c.3269G>C	XP_005254752.1:p.Trp1090Ser
XM_006720700.1:c.3527G>C	XP_006720763.1:p.Trp1176Ser
XM_006720701.2:c.3527G>C	XP_006720764.1:p.Trp1176Ser
XM_006720701.3:c.3527G>C	XP_006720764.1:p.Trp1176Ser
XM_011522093.1:c.3527G>C	XP_011520395.1:p.Trp1176Ser
XM_017022634.1:c.3527G>C	XP_016878123.1:p.Trp1176Ser
XM_017022635.2:c.3527G>C	XP_016878124.1:p.Trp1176Ser
XM_017022636.1:c.404G>C	XP_016878125.1:p.Trp135Ser
XR_001751402.1:n.3558G>C
XR_931917.1:n.3558G>C
XR_931917.2:n.3558G>C