Canonical Allele Identifier: CA2173701229

Gene: SPG11

Linked Data

• dbSNP Id: rs1595863591
• gnomAD v4: 15-44598562-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598562C>G , CM000677.2:g.44598562C>G	GRCh38
NC_000015.9:g.44890760C>G , CM000677.1:g.44890760C>G	GRCh37
NC_000015.8:g.42678052C>G	NCBI36
NG_008885.1:g.70117G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3892+69G>C	ENSP00000453246.2:n.3892+69G>C
ENST00000682065.1:c.3892+69G>C	ENSP00000507025.1:n.3892+69G>C
ENST00000682460.1:c.*312+69G>C	ENSP00000508334.1:n.*312+69G>C
ENST00000682495.1:c.*384+69G>C	ENSP00000507166.1:n.*384+69G>C
ENST00000682669.1:c.3691+69G>C	ENSP00000507782.1:n.3691+69G>C
ENST00000682788.1:c.3892+69G>C	ENSP00000508089.1:n.3892+69G>C
ENST00000683121.1:c.3892+69G>C	ENSP00000507557.1:n.3892+69G>C
ENST00000683186.1:c.*655+69G>C	ENSP00000507268.1:n.*655+69G>C
ENST00000683496.1:c.3892+69G>C	ENSP00000506968.1:n.3892+69G>C
ENST00000683734.1:c.3892+69G>C	ENSP00000508319.1:n.3892+69G>C
ENST00000683753.1:n.2938+69G>C
ENST00000683838.1:n.966+69G>C
ENST00000684038.1:c.*312+69G>C	ENSP00000507141.1:n.*312+69G>C
ENST00000684235.1:c.3892+69G>C	ENSP00000508295.1:n.3892+69G>C
ENST00000684676.1:c.3892+69G>C	ENSP00000506948.1:n.3892+69G>C
ENST00000261866.12:c.3892+69G>C MANE Select	ENSP00000261866.7:n.3892+69G>C
ENST00000261866.11:c.3892+69G>C	ENSP00000261866.7:n.3892+69G>C
ENST00000427534.6:c.3892+69G>C	ENSP00000396110.2:n.3892+69G>C
ENST00000535302.6:c.3892+69G>C	ENSP00000445278.2:n.3892+69G>C
ENST00000558093.1:n.506+69G>C
ENST00000558319.5:c.3892+69G>C	ENSP00000453599.1:n.3892+69G>C
ENST00000558561.1:n.118G>C
NM_001160227.1:c.3892+69G>C	NP_001153699.1:n.3892+69G>C
NM_025137.3:c.3892+69G>C	NP_079413.3:n.3892+69G>C
XM_005254695.3:c.3634+69G>C	XP_005254752.1:n.3634+69G>C
XM_006720700.1:c.3892+69G>C	XP_006720763.1:n.3892+69G>C
XM_006720701.2:c.3892+69G>C	XP_006720764.1:n.3892+69G>C
XM_011522093.1:c.3687-189G>C	XP_011520395.1:n.3687-189G>C
XR_931917.1:n.3923+69G>C
XM_006720701.3:c.3892+69G>C	XP_006720764.1:n.3892+69G>C
XM_017022634.1:c.3892+69G>C	XP_016878123.1:n.3892+69G>C
XM_017022635.2:c.3892+69G>C	XP_016878124.1:n.3892+69G>C
XM_017022636.1:c.769+69G>C	XP_016878125.1:n.769+69G>C
XR_001751402.1:n.3718-189G>C
XR_931917.2:n.3923+69G>C
NM_025137.4:c.3892+69G>C MANE Select	NP_079413.3:n.3892+69G>C
NM_001160227.2:c.3892+69G>C	NP_001153699.1:n.3892+69G>C