Canonical Allele Identifier: CA2568174088

Gene: SPG11

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44608456_44608457insCCAATATT , CM000677.2:g.44608456_44608457insCCAATATT	GRCh38
NC_000015.9:g.44900654_44900655insCCAATATT , CM000677.1:g.44900654_44900655insCCAATATT	GRCh37
NC_000015.8:g.42687946_42687947insCCAATATT	NCBI36
NG_008885.1:g.60222_60223insAATATTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.3440_3441insAATATTGG	ENSP00000453246.2:p.Tyr1147Ter
ENST00000682065.1:c.3440_3441insAATATTGG	ENSP00000507025.1:p.Tyr1147Ter
ENST00000682460.1:c.3440_3441insAATATTGG	ENSP00000508334.1:p.Tyr1147Ter
ENST00000682495.1:c.3440_3441insAATATTGG	ENSP00000507166.1:p.Tyr1147Ter
ENST00000682669.1:c.3440_3441insAATATTGG	ENSP00000507782.1:p.Tyr1147Ter
ENST00000682788.1:c.3440_3441insAATATTGG	ENSP00000508089.1:p.Tyr1147Ter
ENST00000682915.1:c.3440_3441insAATATTGG	ENSP00000507493.1:p.Tyr1147Ter
ENST00000683121.1:c.3440_3441insAATATTGG	ENSP00000507557.1:p.Tyr1147Ter
ENST00000683186.1:c.*270_*271insAATATTGG	ENSP00000507268.1:n.*270_*271insAATATTGG
ENST00000683255.1:c.*270_*271insAATATTGG	ENSP00000508340.1:n.*270_*271insAATATTGG
ENST00000683496.1:c.3440_3441insAATATTGG	ENSP00000506968.1:p.Tyr1147Ter
ENST00000683734.1:c.3440_3441insAATATTGG	ENSP00000508319.1:p.Tyr1147Ter
ENST00000683753.1:n.2486_2487insAATATTGG
ENST00000684038.1:c.3182_3183insAATATTGG	ENSP00000507141.1:p.Tyr1061Ter
ENST00000684235.1:c.3440_3441insAATATTGG	ENSP00000508295.1:p.Tyr1147Ter
ENST00000684676.1:c.3440_3441insAATATTGG	ENSP00000506948.1:p.Tyr1147Ter
ENST00000261866.12:c.3440_3441insAATATTGG MANE Select	ENSP00000261866.7:p.Tyr1147Ter
ENST00000261866.11:c.3440_3441insAATATTGG	ENSP00000261866.7:p.Tyr1147Ter
ENST00000427534.6:c.3440_3441insAATATTGG	ENSP00000396110.2:p.Tyr1147Ter
ENST00000535302.6:c.3440_3441insAATATTGG	ENSP00000445278.2:p.Tyr1147Ter
ENST00000558319.5:c.3440_3441insAATATTGG	ENSP00000453599.1:p.Tyr1147Ter
ENST00000558988.5:c.167_168insAATATTGG	ENSP00000453921.1:p.Tyr56Ter
ENST00000559754.1:c.169_170insAATATTGG
NM_001160227.1:c.3440_3441insAATATTGG	NP_001153699.1:p.Tyr1147Ter
NM_025137.3:c.3440_3441insAATATTGG	NP_079413.3:p.Tyr1147Ter
XM_005254695.3:c.3182_3183insAATATTGG	XP_005254752.1:p.Tyr1061Ter
XM_006720700.1:c.3440_3441insAATATTGG	XP_006720763.1:p.Tyr1147Ter
XM_006720701.2:c.3440_3441insAATATTGG	XP_006720764.1:p.Tyr1147Ter
XM_011522093.1:c.3440_3441insAATATTGG	XP_011520395.1:p.Tyr1147Ter
XR_931917.1:n.3471_3472insAATATTGG
XM_006720701.3:c.3440_3441insAATATTGG	XP_006720764.1:p.Tyr1147Ter
XM_017022634.1:c.3440_3441insAATATTGG	XP_016878123.1:p.Tyr1147Ter
XM_017022635.2:c.3440_3441insAATATTGG	XP_016878124.1:p.Tyr1147Ter
XM_017022636.1:c.317_318insAATATTGG	XP_016878125.1:p.Tyr106Ter
XR_001751402.1:n.3471_3472insAATATTGG
XR_931917.2:n.3471_3472insAATATTGG
NM_025137.4:c.3440_3441insAATATTGG MANE Select	NP_079413.3:p.Tyr1147Ter
NM_001160227.2:c.3440_3441insAATATTGG	NP_001153699.1:p.Tyr1147Ter