Canonical Allele Identifier: CA392230199

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44890947T>A (hg19) ; chr15:g.44598749T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598749T>A , CM000677.2:g.44598749T>A	GRCh38
NC_000015.9:g.44890947T>A , CM000677.1:g.44890947T>A	GRCh37
NC_000015.8:g.42678239T>A	NCBI36
NG_008885.1:g.69930A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3774A>T	ENSP00000453246.2:p.Leu1258Phe
ENST00000682065.1:c.3774A>T	ENSP00000507025.1:p.Leu1258Phe
ENST00000682460.1:c.*194A>T	ENSP00000508334.1:n.*194A>T
ENST00000682495.1:c.*266A>T	ENSP00000507166.1:n.*266A>T
ENST00000682669.1:c.3573A>T	ENSP00000507782.1:p.Leu1191Phe
ENST00000682788.1:c.3774A>T	ENSP00000508089.1:p.Leu1258Phe
ENST00000682915.1:c.3867A>T	ENSP00000507493.1:n.3867A>T
ENST00000683121.1:c.3774A>T	ENSP00000507557.1:p.Leu1258Phe
ENST00000683186.1:c.*537A>T	ENSP00000507268.1:n.*537A>T
ENST00000683496.1:c.3774A>T	ENSP00000506968.1:p.Leu1258Phe
ENST00000683734.1:c.3774A>T	ENSP00000508319.1:p.Leu1258Phe
ENST00000683753.1:n.2820A>T
ENST00000683838.1:n.848A>T
ENST00000684038.1:c.*194A>T	ENSP00000507141.1:n.*194A>T
ENST00000684235.1:c.3774A>T	ENSP00000508295.1:p.Leu1258Phe
ENST00000684676.1:c.3774A>T	ENSP00000506948.1:p.Leu1258Phe
ENST00000261866.12:c.3774A>T MANE Select	ENSP00000261866.7:p.Leu1258Phe
ENST00000261866.11:c.3774A>T	ENSP00000261866.7:p.Leu1258Phe
ENST00000427534.6:c.3774A>T	ENSP00000396110.2:p.Leu1258Phe
ENST00000535302.6:c.3774A>T	ENSP00000445278.2:p.Leu1258Phe
ENST00000558093.1:n.388A>T
ENST00000558319.5:c.3774A>T	ENSP00000453599.1:p.Leu1258Phe
NM_001160227.1:c.3774A>T	NP_001153699.1:p.Leu1258Phe
NM_025137.3:c.3774A>T	NP_079413.3:p.Leu1258Phe
XM_005254695.3:c.3516A>T	XP_005254752.1:p.Leu1172Phe
XM_006720700.1:c.3774A>T	XP_006720763.1:p.Leu1258Phe
XM_006720701.2:c.3774A>T	XP_006720764.1:p.Leu1258Phe
XM_011522093.1:c.3687-376A>T	XP_011520395.1:n.3687-376A>T
XR_931917.1:n.3805A>T
XM_006720701.3:c.3774A>T	XP_006720764.1:p.Leu1258Phe
XM_017022634.1:c.3774A>T	XP_016878123.1:p.Leu1258Phe
XM_017022635.2:c.3774A>T	XP_016878124.1:p.Leu1258Phe
XM_017022636.1:c.651A>T	XP_016878125.1:p.Leu217Phe
XR_001751402.1:n.3718-376A>T
XR_931917.2:n.3805A>T
NM_025137.4:c.3774A>T MANE Select	NP_079413.3:p.Leu1258Phe
NM_001160227.2:c.3774A>T	NP_001153699.1:p.Leu1258Phe