Canonical Allele Identifier: CA2628203091

Gene: SPG11

Linked Data

• gnomAD v4: 15-44575180-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575180A>G , CM000677.2:g.44575180A>G	GRCh38
NC_000015.9:g.44867378A>G , CM000677.1:g.44867378A>G	GRCh37
NC_000015.8:g.42654670A>G	NCBI36
NG_008885.1:g.93499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4522T>C	ENSP00000453246.2:n.5867-4522T>C
ENST00000561391.2:n.2095-139T>C
ENST00000682065.1:c.5723-139T>C	ENSP00000507025.1:n.5723-139T>C
ENST00000682460.1:c.*2124-139T>C	ENSP00000508334.1:n.*2124-139T>C
ENST00000682495.1:c.*2359-139T>C	ENSP00000507166.1:n.*2359-139T>C
ENST00000682669.1:c.5666-139T>C	ENSP00000507782.1:n.5666-139T>C
ENST00000683186.1:c.*2630-139T>C	ENSP00000507268.1:n.*2630-139T>C
ENST00000683496.1:c.5867-139T>C	ENSP00000506968.1:n.5867-139T>C
ENST00000683734.1:c.5867-1435T>C	ENSP00000508319.1:n.5867-1435T>C
ENST00000683753.1:n.4913-139T>C
ENST00000684038.1:c.*2287-139T>C	ENSP00000507141.1:n.*2287-139T>C
ENST00000684235.1:c.5867-139T>C	ENSP00000508295.1:n.5867-139T>C
ENST00000684676.1:c.*16-139T>C	ENSP00000506948.1:n.*16-139T>C
ENST00000261866.12:c.5867-139T>C MANE Select	ENSP00000261866.7:n.5867-139T>C
ENST00000261866.11:c.5867-139T>C	ENSP00000261866.7:n.5867-139T>C
ENST00000427534.6:c.5867-139T>C	ENSP00000396110.2:n.5867-139T>C
ENST00000535302.6:c.5867-2360T>C	ENSP00000445278.2:n.5867-2360T>C
ENST00000558080.1:n.93T>C
ENST00000558319.5:c.5867-139T>C	ENSP00000453599.1:n.5867-139T>C
ENST00000559511.5:c.715-4522T>C
ENST00000559822.1:c.410-139T>C
NM_001160227.1:c.5867-2360T>C	NP_001153699.1:n.5867-2360T>C
NM_025137.3:c.5867-139T>C	NP_079413.3:n.5867-139T>C
XM_005254695.3:c.5609-139T>C	XP_005254752.1:n.5609-139T>C
XM_006720700.1:c.5723-139T>C	XP_006720763.1:n.5723-139T>C
XM_017022634.1:c.5867-139T>C	XP_016878123.1:n.5867-139T>C
XM_017022636.1:c.2744-139T>C	XP_016878125.1:n.2744-139T>C
NM_025137.4:c.5867-139T>C MANE Select	NP_079413.3:n.5867-139T>C
NM_001160227.2:c.5867-2360T>C	NP_001153699.1:n.5867-2360T>C