Canonical Allele Identifier: CA2628202693

Gene: SPG11

Linked Data

• gnomAD v4: 15-44574873-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44574873A>G , CM000677.2:g.44574873A>G	GRCh38
NC_000015.9:g.44867071A>G , CM000677.1:g.44867071A>G	GRCh37
NC_000015.8:g.42654363A>G	NCBI36
NG_008885.1:g.93806T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000559511.6:c.5867-4215T>C	ENSP00000453246.2:n.5867-4215T>C
ENST00000561391.2:n.2234+29T>C
ENST00000682065.1:c.5862+29T>C	ENSP00000507025.1:n.5862+29T>C
ENST00000682460.1:c.*2263+29T>C	ENSP00000508334.1:n.*2263+29T>C
ENST00000682495.1:c.*2498+29T>C	ENSP00000507166.1:n.*2498+29T>C
ENST00000682669.1:c.5805+29T>C	ENSP00000507782.1:n.5805+29T>C
ENST00000683186.1:c.*2769+29T>C	ENSP00000507268.1:n.*2769+29T>C
ENST00000683496.1:c.6006+29T>C	ENSP00000506968.1:n.6006+29T>C
ENST00000683734.1:c.5867-1128T>C	ENSP00000508319.1:n.5867-1128T>C
ENST00000683753.1:n.5052+29T>C
ENST00000684038.1:c.*2426+29T>C	ENSP00000507141.1:n.*2426+29T>C
ENST00000684235.1:c.6006+29T>C	ENSP00000508295.1:n.6006+29T>C
ENST00000684676.1:c.*155+29T>C	ENSP00000506948.1:n.*155+29T>C
ENST00000261866.12:c.6006+29T>C MANE Select	ENSP00000261866.7:n.6006+29T>C
ENST00000261866.11:c.6006+29T>C	ENSP00000261866.7:n.6006+29T>C
ENST00000427534.6:c.6006+29T>C	ENSP00000396110.2:n.6006+29T>C
ENST00000535302.6:c.5867-2053T>C	ENSP00000445278.2:n.5867-2053T>C
ENST00000558080.1:n.371+29T>C
ENST00000558319.5:c.6006+29T>C	ENSP00000453599.1:n.6006+29T>C
ENST00000559511.5:c.715-4215T>C
ENST00000559822.1:c.549+29T>C
NM_001160227.1:c.5867-2053T>C	NP_001153699.1:n.5867-2053T>C
NM_025137.3:c.6006+29T>C	NP_079413.3:n.6006+29T>C
XM_005254695.3:c.5748+29T>C	XP_005254752.1:n.5748+29T>C
XM_006720700.1:c.5862+29T>C	XP_006720763.1:n.5862+29T>C
XM_017022634.1:c.6006+29T>C	XP_016878123.1:n.6006+29T>C
XM_017022636.1:c.2883+29T>C	XP_016878125.1:n.2883+29T>C
NM_025137.4:c.6006+29T>C MANE Select	NP_079413.3:n.6006+29T>C
NM_001160227.2:c.5867-2053T>C	NP_001153699.1:n.5867-2053T>C