Canonical Allele Identifier: CA392218129

Gene: SPG11

Linked Data

• gnomAD v4: 15-44573567-A-G
• MyVariant Identifiers: chr15:g.44865765A>G (hg19) ; chr15:g.44573567A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44573567A>G , CM000677.2:g.44573567A>G	GRCh38
NC_000015.9:g.44865765A>G , CM000677.1:g.44865765A>G	GRCh37
NC_000015.8:g.42653057A>G	NCBI36
NG_008885.1:g.95112T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-2909T>C	ENSP00000453246.2:n.5867-2909T>C
ENST00000561391.2:n.2413T>C
ENST00000682065.1:c.6041T>C	ENSP00000507025.1:p.Leu2014Pro
ENST00000682460.1:c.*2442T>C	ENSP00000508334.1:n.*2442T>C
ENST00000682495.1:c.*2677T>C	ENSP00000507166.1:n.*2677T>C
ENST00000682669.1:c.5984T>C	ENSP00000507782.1:p.Leu1995Pro
ENST00000683186.1:c.*2948T>C	ENSP00000507268.1:n.*2948T>C
ENST00000683496.1:c.6006+1335T>C	ENSP00000506968.1:n.6006+1335T>C
ENST00000683734.1:c.*135T>C	ENSP00000508319.1:n.*135T>C
ENST00000683753.1:n.5231T>C
ENST00000684038.1:c.*2605T>C	ENSP00000507141.1:n.*2605T>C
ENST00000684235.1:c.6185T>C	ENSP00000508295.1:p.Leu2062Pro
ENST00000684676.1:c.*334T>C	ENSP00000506948.1:n.*334T>C
ENST00000261866.12:c.6185T>C MANE Select	ENSP00000261866.7:p.Leu2062Pro
ENST00000261866.11:c.6185T>C	ENSP00000261866.7:p.Leu2062Pro
ENST00000427534.6:c.6185T>C	ENSP00000396110.2:p.Leu2062Pro
ENST00000535302.6:c.5867-747T>C	ENSP00000445278.2:n.5867-747T>C
ENST00000558080.1:n.550T>C
ENST00000558319.5:c.6185T>C	ENSP00000453599.1:p.Leu2062Pro
ENST00000559511.5:c.715-2909T>C
ENST00000559933.1:n.254T>C
ENST00000561268.5:n.117T>C
NM_001160227.1:c.5867-747T>C	NP_001153699.1:n.5867-747T>C
NM_025137.3:c.6185T>C	NP_079413.3:p.Leu2062Pro
XM_005254695.3:c.5927T>C	XP_005254752.1:p.Leu1976Pro
XM_006720700.1:c.6041T>C	XP_006720763.1:p.Leu2014Pro
XM_017022634.1:c.6185T>C	XP_016878123.1:p.Leu2062Pro
XM_017022636.1:c.3062T>C	XP_016878125.1:p.Leu1021Pro
NM_025137.4:c.6185T>C MANE Select	NP_079413.3:p.Leu2062Pro
NM_001160227.2:c.5867-747T>C	NP_001153699.1:n.5867-747T>C