Canonical Allele Identifier: CA392230000

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44890869T>A (hg19) ; chr15:g.44598671T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598671T>A , CM000677.2:g.44598671T>A	GRCh38
NC_000015.9:g.44890869T>A , CM000677.1:g.44890869T>A	GRCh37
NC_000015.8:g.42678161T>A	NCBI36
NG_008885.1:g.70008A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3852A>T	ENSP00000453246.2:p.Arg1284Ser
ENST00000682065.1:c.3852A>T	ENSP00000507025.1:p.Arg1284Ser
ENST00000682460.1:c.*272A>T	ENSP00000508334.1:n.*272A>T
ENST00000682495.1:c.*344A>T	ENSP00000507166.1:n.*344A>T
ENST00000682669.1:c.3651A>T	ENSP00000507782.1:p.Arg1217Ser
ENST00000682788.1:c.3852A>T	ENSP00000508089.1:p.Arg1284Ser
ENST00000682915.1:c.3945A>T	ENSP00000507493.1:n.3945A>T
ENST00000683121.1:c.3852A>T	ENSP00000507557.1:p.Arg1284Ser
ENST00000683186.1:c.*615A>T	ENSP00000507268.1:n.*615A>T
ENST00000683496.1:c.3852A>T	ENSP00000506968.1:p.Arg1284Ser
ENST00000683734.1:c.3852A>T	ENSP00000508319.1:p.Arg1284Ser
ENST00000683753.1:n.2898A>T
ENST00000683838.1:n.926A>T
ENST00000684038.1:c.*272A>T	ENSP00000507141.1:n.*272A>T
ENST00000684235.1:c.3852A>T	ENSP00000508295.1:p.Arg1284Ser
ENST00000684676.1:c.3852A>T	ENSP00000506948.1:p.Arg1284Ser
ENST00000261866.12:c.3852A>T MANE Select	ENSP00000261866.7:p.Arg1284Ser
ENST00000261866.11:c.3852A>T	ENSP00000261866.7:p.Arg1284Ser
ENST00000427534.6:c.3852A>T	ENSP00000396110.2:p.Arg1284Ser
ENST00000535302.6:c.3852A>T	ENSP00000445278.2:p.Arg1284Ser
ENST00000558093.1:n.466A>T
ENST00000558319.5:c.3852A>T	ENSP00000453599.1:p.Arg1284Ser
ENST00000558561.1:n.9A>T
NM_001160227.1:c.3852A>T	NP_001153699.1:p.Arg1284Ser
NM_025137.3:c.3852A>T	NP_079413.3:p.Arg1284Ser
XM_005254695.3:c.3594A>T	XP_005254752.1:p.Arg1198Ser
XM_006720700.1:c.3852A>T	XP_006720763.1:p.Arg1284Ser
XM_006720701.2:c.3852A>T	XP_006720764.1:p.Arg1284Ser
XM_011522093.1:c.3687-298A>T	XP_011520395.1:n.3687-298A>T
XR_931917.1:n.3883A>T
XM_006720701.3:c.3852A>T	XP_006720764.1:p.Arg1284Ser
XM_017022634.1:c.3852A>T	XP_016878123.1:p.Arg1284Ser
XM_017022635.2:c.3852A>T	XP_016878124.1:p.Arg1284Ser
XM_017022636.1:c.729A>T	XP_016878125.1:p.Arg243Ser
XR_001751402.1:n.3718-298A>T
XR_931917.2:n.3883A>T
NM_025137.4:c.3852A>T MANE Select	NP_079413.3:p.Arg1284Ser
NM_001160227.2:c.3852A>T	NP_001153699.1:p.Arg1284Ser