Canonical Allele Identifier: CA392219140

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44867220C>G (hg19) ; chr15:g.44575022C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575022C>G , CM000677.2:g.44575022C>G	GRCh38
NC_000015.9:g.44867220C>G , CM000677.1:g.44867220C>G	GRCh37
NC_000015.8:g.42654512C>G	NCBI36
NG_008885.1:g.93657G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4364G>C	ENSP00000453246.2:n.5867-4364G>C
ENST00000561391.2:n.2114G>C
ENST00000682065.1:c.5742G>C	ENSP00000507025.1:p.Gln1914His
ENST00000682460.1:c.*2143G>C	ENSP00000508334.1:n.*2143G>C
ENST00000682495.1:c.*2378G>C	ENSP00000507166.1:n.*2378G>C
ENST00000682669.1:c.5685G>C	ENSP00000507782.1:p.Gln1895His
ENST00000683186.1:c.*2649G>C	ENSP00000507268.1:n.*2649G>C
ENST00000683496.1:c.5886G>C	ENSP00000506968.1:p.Gln1962His
ENST00000683734.1:c.5867-1277G>C	ENSP00000508319.1:n.5867-1277G>C
ENST00000683753.1:n.4932G>C
ENST00000684038.1:c.*2306G>C	ENSP00000507141.1:n.*2306G>C
ENST00000684235.1:c.5886G>C	ENSP00000508295.1:p.Gln1962His
ENST00000684676.1:c.*35G>C	ENSP00000506948.1:n.*35G>C
ENST00000261866.12:c.5886G>C MANE Select	ENSP00000261866.7:p.Gln1962His
ENST00000261866.11:c.5886G>C	ENSP00000261866.7:p.Gln1962His
ENST00000427534.6:c.5886G>C	ENSP00000396110.2:p.Gln1962His
ENST00000535302.6:c.5867-2202G>C	ENSP00000445278.2:n.5867-2202G>C
ENST00000558080.1:n.251G>C
ENST00000558319.5:c.5886G>C	ENSP00000453599.1:p.Gln1962His
ENST00000559511.5:c.715-4364G>C
ENST00000559822.1:c.429G>C
NM_001160227.1:c.5867-2202G>C	NP_001153699.1:n.5867-2202G>C
NM_025137.3:c.5886G>C	NP_079413.3:p.Gln1962His
XM_005254695.3:c.5628G>C	XP_005254752.1:p.Gln1876His
XM_006720700.1:c.5742G>C	XP_006720763.1:p.Gln1914His
XM_017022634.1:c.5886G>C	XP_016878123.1:p.Gln1962His
XM_017022636.1:c.2763G>C	XP_016878125.1:p.Gln921His
NM_025137.4:c.5886G>C MANE Select	NP_079413.3:p.Gln1962His
NM_001160227.2:c.5867-2202G>C	NP_001153699.1:n.5867-2202G>C