Canonical Allele Identifier: CA270081941

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44585818G>A , CM000677.2:g.44585818G>A	GRCh38
NC_000015.9:g.44878016G>A , CM000677.1:g.44878016G>A	GRCh37
NC_000015.8:g.42665308G>A	NCBI36
NG_008885.1:g.82861C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025137.4:c.4939C>T MANE Select	NP_079413.3:p.Gln1647Ter
ENST00000261866.12:c.4939C>T MANE Select	ENSP00000261866.7:p.Gln1647Ter
NM_001160227.1:c.4939C>T	NP_001153699.1:p.Gln1647Ter
NM_001160227.2:c.4939C>T	NP_001153699.1:p.Gln1647Ter
NM_025137.3:c.4939C>T	NP_079413.3:p.Gln1647Ter
ENST00000261866.11:c.4939C>T	ENSP00000261866.7:p.Gln1647Ter
ENST00000427534.6:c.4939C>T	ENSP00000396110.2:p.Gln1647Ter
ENST00000535302.6:c.4939C>T	ENSP00000445278.2:p.Gln1647Ter
ENST00000558253.5:n.713C>T
ENST00000558319.5:c.4939C>T	ENSP00000453599.1:p.Gln1647Ter
ENST00000558790.5:n.376C>T
ENST00000559511.6:c.4939C>T	ENSP00000453246.2:p.Gln1647Ter
ENST00000560858.1:c.391C>T	ENSP00000452991.1:n.391C>T
ENST00000561391.2:n.1167C>T
ENST00000682065.1:c.4939C>T	ENSP00000507025.1:p.Gln1647Ter
ENST00000682460.1:c.*1196C>T	ENSP00000508334.1:n.*1196C>T
ENST00000682495.1:c.*1431C>T	ENSP00000507166.1:n.*1431C>T
ENST00000682669.1:c.4738C>T	ENSP00000507782.1:p.Gln1580Ter
ENST00000682788.1:c.*91C>T	ENSP00000508089.1:n.*91C>T
ENST00000683186.1:c.*1702C>T	ENSP00000507268.1:n.*1702C>T
ENST00000683496.1:c.4939C>T	ENSP00000506968.1:p.Gln1647Ter
ENST00000683734.1:c.4939C>T	ENSP00000508319.1:p.Gln1647Ter
ENST00000683753.1:n.3985C>T
ENST00000684038.1:c.*1359C>T	ENSP00000507141.1:n.*1359C>T
ENST00000684235.1:c.4939C>T	ENSP00000508295.1:p.Gln1647Ter
ENST00000684676.1:c.4939C>T	ENSP00000506948.1:p.Gln1647Ter
XM_005254695.3:c.4681C>T	XP_005254752.1:p.Gln1561Ter
XM_006720700.1:c.4939C>T	XP_006720763.1:p.Gln1647Ter
XM_006720701.2:c.*21C>T	XP_006720764.1:n.*21C>T
XM_006720701.3:c.*21C>T	XP_006720764.1:n.*21C>T
XM_017022634.1:c.4939C>T	XP_016878123.1:p.Gln1647Ter
XM_017022636.1:c.1816C>T	XP_016878125.1:p.Gln606Ter
XR_931917.2:n.4993C>T