Canonical Allele Identifier: CA7534815

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44598334G>A , CM000677.2:g.44598334G>A	GRCh38
NC_000015.9:g.44890532G>A , CM000677.1:g.44890532G>A	GRCh37
NC_000015.8:g.42677824G>A	NCBI36
NG_008885.1:g.70345C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.3932C>T MANE Select	NP_079413.3:p.Thr1311Ile
ENST00000261866.12:c.3932C>T MANE Select	ENSP00000261866.7:p.Thr1311Ile
NM_001160227.1:c.3932C>T	NP_001153699.1:p.Thr1311Ile
NM_001160227.2:c.3932C>T	NP_001153699.1:p.Thr1311Ile
NM_025137.3:c.3932C>T	NP_079413.3:p.Thr1311Ile
ENST00000261866.11:c.3932C>T	ENSP00000261866.7:p.Thr1311Ile
ENST00000427534.6:c.3932C>T	ENSP00000396110.2:p.Thr1311Ile
ENST00000535302.6:c.3932C>T	ENSP00000445278.2:p.Thr1311Ile
ENST00000558319.5:c.3932C>T	ENSP00000453599.1:p.Thr1311Ile
ENST00000558561.1:n.346C>T
ENST00000559511.6:c.3932C>T	ENSP00000453246.2:p.Thr1311Ile
ENST00000682065.1:c.3932C>T	ENSP00000507025.1:p.Thr1311Ile
ENST00000682460.1:c.*352C>T	ENSP00000508334.1:n.*352C>T
ENST00000682495.1:c.*424C>T	ENSP00000507166.1:n.*424C>T
ENST00000682669.1:c.3731C>T	ENSP00000507782.1:p.Thr1244Ile
ENST00000682788.1:c.3932C>T	ENSP00000508089.1:p.Thr1311Ile
ENST00000683121.1:c.3932C>T	ENSP00000507557.1:p.Thr1311Ile
ENST00000683186.1:c.*695C>T	ENSP00000507268.1:n.*695C>T
ENST00000683496.1:c.3932C>T	ENSP00000506968.1:p.Thr1311Ile
ENST00000683734.1:c.3932C>T	ENSP00000508319.1:p.Thr1311Ile
ENST00000683753.1:n.2978C>T
ENST00000683838.1:n.1006C>T
ENST00000684038.1:c.*352C>T	ENSP00000507141.1:n.*352C>T
ENST00000684235.1:c.3932C>T	ENSP00000508295.1:p.Thr1311Ile
ENST00000684676.1:c.3932C>T	ENSP00000506948.1:p.Thr1311Ile
XM_005254695.3:c.3674C>T	XP_005254752.1:p.Thr1225Ile
XM_006720700.1:c.3932C>T	XP_006720763.1:p.Thr1311Ile
XM_006720701.2:c.3932C>T	XP_006720764.1:p.Thr1311Ile
XM_006720701.3:c.3932C>T	XP_006720764.1:p.Thr1311Ile
XM_011522093.1:c.*24C>T	XP_011520395.1:n.*24C>T
XM_017022634.1:c.3932C>T	XP_016878123.1:p.Thr1311Ile
XM_017022635.2:c.3932C>T	XP_016878124.1:p.Thr1311Ile
XM_017022636.1:c.809C>T	XP_016878125.1:p.Thr270Ile
XR_001751402.1:n.3757C>T
XR_931917.1:n.3963C>T
XR_931917.2:n.3963C>T