Canonical Allele Identifier: CA7534902

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44600595G>C , CM000677.2:g.44600595G>C	GRCh38
NC_000015.9:g.44892793G>C , CM000677.1:g.44892793G>C	GRCh37
NC_000015.8:g.42680085G>C	NCBI36
NG_008885.1:g.68084C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.3558C>G MANE Select	NP_079413.3:p.Asp1186Glu
ENST00000261866.12:c.3558C>G MANE Select	ENSP00000261866.7:p.Asp1186Glu
NM_001160227.1:c.3558C>G	NP_001153699.1:p.Asp1186Glu
NM_001160227.2:c.3558C>G	NP_001153699.1:p.Asp1186Glu
NM_025137.3:c.3558C>G	NP_079413.3:p.Asp1186Glu
ENST00000261866.11:c.3558C>G	ENSP00000261866.7:p.Asp1186Glu
ENST00000427534.6:c.3558C>G	ENSP00000396110.2:p.Asp1186Glu
ENST00000535302.6:c.3558C>G	ENSP00000445278.2:p.Asp1186Glu
ENST00000558093.1:n.172C>G
ENST00000558319.5:c.3558C>G	ENSP00000453599.1:p.Asp1186Glu
ENST00000558988.5:c.285C>G	ENSP00000453921.1:p.Asp95Glu
ENST00000559511.6:c.3558C>G	ENSP00000453246.2:p.Asp1186Glu
ENST00000559754.1:c.380C>G
ENST00000682065.1:c.3558C>G	ENSP00000507025.1:p.Asp1186Glu
ENST00000682460.1:c.3644C>G	ENSP00000508334.1:p.Thr1215Ser
ENST00000682495.1:c.*50C>G	ENSP00000507166.1:n.*50C>G
ENST00000682669.1:c.3454-97C>G	ENSP00000507782.1:n.3454-97C>G
ENST00000682788.1:c.3558C>G	ENSP00000508089.1:p.Asp1186Glu
ENST00000682915.1:c.3651C>G	ENSP00000507493.1:n.3651C>G
ENST00000683121.1:c.3558C>G	ENSP00000507557.1:p.Asp1186Glu
ENST00000683186.1:c.*321C>G	ENSP00000507268.1:n.*321C>G
ENST00000683496.1:c.3558C>G	ENSP00000506968.1:p.Asp1186Glu
ENST00000683734.1:c.3558C>G	ENSP00000508319.1:p.Asp1186Glu
ENST00000683753.1:n.2604C>G
ENST00000683838.1:n.632C>G
ENST00000684038.1:c.3386C>G	ENSP00000507141.1:p.Thr1129Ser
ENST00000684235.1:c.3558C>G	ENSP00000508295.1:p.Asp1186Glu
ENST00000684676.1:c.3558C>G	ENSP00000506948.1:p.Asp1186Glu
XM_005254695.3:c.3300C>G	XP_005254752.1:p.Asp1100Glu
XM_006720700.1:c.3558C>G	XP_006720763.1:p.Asp1186Glu
XM_006720701.2:c.3558C>G	XP_006720764.1:p.Asp1186Glu
XM_006720701.3:c.3558C>G	XP_006720764.1:p.Asp1186Glu
XM_011522093.1:c.3558C>G	XP_011520395.1:p.Asp1186Glu
XM_017022634.1:c.3558C>G	XP_016878123.1:p.Asp1186Glu
XM_017022635.2:c.3558C>G	XP_016878124.1:p.Asp1186Glu
XM_017022636.1:c.435C>G	XP_016878125.1:p.Asp145Glu
XR_001751402.1:n.3589C>G
XR_931917.1:n.3589C>G
XR_931917.2:n.3589C>G