Canonical Allele Identifier: CA270110639

Gene: SPG11

Linked Data

• dbSNP Id: rs766299285
• gnomAD v2: 15-44952549-CTA-C
• gnomAD v3: 15-44660351-CTA-C
• gnomAD v4: 15-44660351-CTA-C
• MyVariant Identifiers: chr15:g.44952550_44952551del (hg19) ; chr15:g.44660352_44660353del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44660353_44660354del , CM000677.2:g.44660353_44660354del	GRCh38
NC_000015.9:g.44952551_44952552del , CM000677.1:g.44952551_44952552del	GRCh37
NC_000015.8:g.42739843_42739844del	NCBI36
NG_008885.1:g.8326_8327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.442+79_442+80del	ENSP00000453246.2:n.442+79_442+80del
ENST00000682065.1:c.442+79_442+80del	ENSP00000507025.1:n.442+79_442+80del
ENST00000682410.1:n.471+79_471+80del
ENST00000682460.1:c.442+79_442+80del	ENSP00000508334.1:n.442+79_442+80del
ENST00000682495.1:c.442+79_442+80del	ENSP00000507166.1:n.442+79_442+80del
ENST00000682648.1:n.387+79_387+80del
ENST00000682669.1:c.442+79_442+80del	ENSP00000507782.1:n.442+79_442+80del
ENST00000682788.1:c.442+79_442+80del	ENSP00000508089.1:n.442+79_442+80del
ENST00000682877.1:n.473+79_473+80del
ENST00000682915.1:c.442+79_442+80del	ENSP00000507493.1:n.442+79_442+80del
ENST00000683121.1:c.442+79_442+80del	ENSP00000507557.1:n.442+79_442+80del
ENST00000683186.1:c.442+79_442+80del	ENSP00000507268.1:n.442+79_442+80del
ENST00000683255.1:c.442+79_442+80del	ENSP00000508340.1:n.442+79_442+80del
ENST00000683496.1:c.442+79_442+80del	ENSP00000506968.1:n.442+79_442+80del
ENST00000683573.1:c.442+79_442+80del	ENSP00000508031.1:n.442+79_442+80del
ENST00000683734.1:c.442+79_442+80del	ENSP00000508319.1:n.442+79_442+80del
ENST00000684038.1:c.442+79_442+80del	ENSP00000507141.1:n.442+79_442+80del
ENST00000684235.1:c.442+79_442+80del	ENSP00000508295.1:n.442+79_442+80del
ENST00000684490.1:n.457+79_457+80del
ENST00000684676.1:c.442+79_442+80del	ENSP00000506948.1:n.442+79_442+80del
ENST00000261866.12:c.442+79_442+80del MANE Select	ENSP00000261866.7:n.442+79_442+80del
ENST00000261866.11:c.442+79_442+80del	ENSP00000261866.7:n.442+79_442+80del
ENST00000427534.6:c.442+79_442+80del	ENSP00000396110.2:n.442+79_442+80del
ENST00000535302.6:c.442+79_442+80del	ENSP00000445278.2:n.442+79_442+80del
ENST00000558319.5:c.442+79_442+80del	ENSP00000453599.1:n.442+79_442+80del
ENST00000559193.5:c.442+79_442+80del	ENSP00000453848.1:n.442+79_442+80del
NM_001160227.1:c.442+79_442+80del	NP_001153699.1:n.442+79_442+80del
NM_025137.3:c.442+79_442+80del	NP_079413.3:n.442+79_442+80del
XM_005254695.3:c.442+79_442+80del	XP_005254752.1:n.442+79_442+80del
XM_006720700.1:c.442+79_442+80del	XP_006720763.1:n.442+79_442+80del
XM_006720701.2:c.442+79_442+80del	XP_006720764.1:n.442+79_442+80del
XM_011522093.1:c.442+79_442+80del	XP_011520395.1:n.442+79_442+80del
XR_931917.1:n.473+79_473+80del
XM_006720701.3:c.442+79_442+80del	XP_006720764.1:n.442+79_442+80del
XM_017022634.1:c.442+79_442+80del	XP_016878123.1:n.442+79_442+80del
XM_017022635.2:c.442+79_442+80del	XP_016878124.1:n.442+79_442+80del
XR_001751402.1:n.473+79_473+80del
XR_931917.2:n.473+79_473+80del
NM_025137.4:c.442+79_442+80del MANE Select	NP_079413.3:n.442+79_442+80del
NM_001160227.2:c.442+79_442+80del	NP_001153699.1:n.442+79_442+80del