Canonical Allele Identifier: CA490203684

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44867229C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44575031C>A , CM000677.2:g.44575031C>A	GRCh38
NC_000015.9:g.44867229C>A , CM000677.1:g.44867229C>A	GRCh37
NC_000015.8:g.42654521C>A	NCBI36
NG_008885.1:g.93648G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5867-4373G>T	ENSP00000453246.2:n.5867-4373G>T
ENST00000561391.2:n.2105G>T
ENST00000682065.1:c.5733G>T	ENSP00000507025.1:p.Leu1911=
ENST00000682460.1:c.*2134G>T	ENSP00000508334.1:n.*2134G>T
ENST00000682495.1:c.*2369G>T	ENSP00000507166.1:n.*2369G>T
ENST00000682669.1:c.5676G>T	ENSP00000507782.1:p.Leu1892=
ENST00000683186.1:c.*2640G>T	ENSP00000507268.1:n.*2640G>T
ENST00000683496.1:c.5877G>T	ENSP00000506968.1:p.Leu1959=
ENST00000683734.1:c.5867-1286G>T	ENSP00000508319.1:n.5867-1286G>T
ENST00000683753.1:n.4923G>T
ENST00000684038.1:c.*2297G>T	ENSP00000507141.1:n.*2297G>T
ENST00000684235.1:c.5877G>T	ENSP00000508295.1:p.Leu1959=
ENST00000684676.1:c.*26G>T	ENSP00000506948.1:n.*26G>T
ENST00000261866.12:c.5877G>T MANE Select	ENSP00000261866.7:p.Leu1959=
ENST00000261866.11:c.5877G>T	ENSP00000261866.7:p.Leu1959=
ENST00000427534.6:c.5877G>T	ENSP00000396110.2:p.Leu1959=
ENST00000535302.6:c.5867-2211G>T	ENSP00000445278.2:n.5867-2211G>T
ENST00000558080.1:n.242G>T
ENST00000558319.5:c.5877G>T	ENSP00000453599.1:p.Leu1959=
ENST00000559511.5:c.715-4373G>T
ENST00000559822.1:c.420G>T
NM_001160227.1:c.5867-2211G>T	NP_001153699.1:n.5867-2211G>T
NM_025137.3:c.5877G>T	NP_079413.3:p.Leu1959=
XM_005254695.3:c.5619G>T	XP_005254752.1:p.Leu1873=
XM_006720700.1:c.5733G>T	XP_006720763.1:p.Leu1911=
XM_017022634.1:c.5877G>T	XP_016878123.1:p.Leu1959=
XM_017022636.1:c.2754G>T	XP_016878125.1:p.Leu918=
NM_025137.4:c.5877G>T MANE Select	NP_079413.3:p.Leu1959=
NM_001160227.2:c.5867-2211G>T	NP_001153699.1:n.5867-2211G>T