Canonical Allele Identifier: CA392230246

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44890957A>T (hg19) ; chr15:g.44598759A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598759A>T , CM000677.2:g.44598759A>T	GRCh38
NC_000015.9:g.44890957A>T , CM000677.1:g.44890957A>T	GRCh37
NC_000015.8:g.42678249A>T	NCBI36
NG_008885.1:g.69920T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3764T>A	ENSP00000453246.2:p.Val1255Asp
ENST00000682065.1:c.3764T>A	ENSP00000507025.1:p.Val1255Asp
ENST00000682460.1:c.*184T>A	ENSP00000508334.1:n.*184T>A
ENST00000682495.1:c.*256T>A	ENSP00000507166.1:n.*256T>A
ENST00000682669.1:c.3563T>A	ENSP00000507782.1:p.Val1188Asp
ENST00000682788.1:c.3764T>A	ENSP00000508089.1:p.Val1255Asp
ENST00000682915.1:c.3857T>A	ENSP00000507493.1:n.3857T>A
ENST00000683121.1:c.3764T>A	ENSP00000507557.1:p.Val1255Asp
ENST00000683186.1:c.*527T>A	ENSP00000507268.1:n.*527T>A
ENST00000683496.1:c.3764T>A	ENSP00000506968.1:p.Val1255Asp
ENST00000683734.1:c.3764T>A	ENSP00000508319.1:p.Val1255Asp
ENST00000683753.1:n.2810T>A
ENST00000683838.1:n.838T>A
ENST00000684038.1:c.*184T>A	ENSP00000507141.1:n.*184T>A
ENST00000684235.1:c.3764T>A	ENSP00000508295.1:p.Val1255Asp
ENST00000684676.1:c.3764T>A	ENSP00000506948.1:p.Val1255Asp
ENST00000261866.12:c.3764T>A MANE Select	ENSP00000261866.7:p.Val1255Asp
ENST00000261866.11:c.3764T>A	ENSP00000261866.7:p.Val1255Asp
ENST00000427534.6:c.3764T>A	ENSP00000396110.2:p.Val1255Asp
ENST00000535302.6:c.3764T>A	ENSP00000445278.2:p.Val1255Asp
ENST00000558093.1:n.378T>A
ENST00000558319.5:c.3764T>A	ENSP00000453599.1:p.Val1255Asp
NM_001160227.1:c.3764T>A	NP_001153699.1:p.Val1255Asp
NM_025137.3:c.3764T>A	NP_079413.3:p.Val1255Asp
XM_005254695.3:c.3506T>A	XP_005254752.1:p.Val1169Asp
XM_006720700.1:c.3764T>A	XP_006720763.1:p.Val1255Asp
XM_006720701.2:c.3764T>A	XP_006720764.1:p.Val1255Asp
XM_011522093.1:c.3687-386T>A	XP_011520395.1:n.3687-386T>A
XR_931917.1:n.3795T>A
XM_006720701.3:c.3764T>A	XP_006720764.1:p.Val1255Asp
XM_017022634.1:c.3764T>A	XP_016878123.1:p.Val1255Asp
XM_017022635.2:c.3764T>A	XP_016878124.1:p.Val1255Asp
XM_017022636.1:c.641T>A	XP_016878125.1:p.Val214Asp
XR_001751402.1:n.3718-386T>A
XR_931917.2:n.3795T>A
NM_025137.4:c.3764T>A MANE Select	NP_079413.3:p.Val1255Asp
NM_001160227.2:c.3764T>A	NP_001153699.1:p.Val1255Asp