Canonical Allele Identifier: CA392222747

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44876533C>A (hg19) ; chr15:g.44584335C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44584335C>A , CM000677.2:g.44584335C>A	GRCh38
NC_000015.9:g.44876533C>A , CM000677.1:g.44876533C>A	GRCh37
NC_000015.8:g.42663825C>A	NCBI36
NG_008885.1:g.84344G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5345G>T	ENSP00000453246.2:p.Trp1782Leu
ENST00000561391.2:n.1573G>T
ENST00000682065.1:c.5201G>T	ENSP00000507025.1:p.Trp1734Leu
ENST00000682460.1:c.*1602G>T	ENSP00000508334.1:n.*1602G>T
ENST00000682495.1:c.*1837G>T	ENSP00000507166.1:n.*1837G>T
ENST00000682669.1:c.5144G>T	ENSP00000507782.1:p.Trp1715Leu
ENST00000683186.1:c.*2108G>T	ENSP00000507268.1:n.*2108G>T
ENST00000683496.1:c.5345G>T	ENSP00000506968.1:p.Trp1782Leu
ENST00000683734.1:c.5345G>T	ENSP00000508319.1:p.Trp1782Leu
ENST00000683753.1:n.4391G>T
ENST00000684038.1:c.*1765G>T	ENSP00000507141.1:n.*1765G>T
ENST00000684235.1:c.5345G>T	ENSP00000508295.1:p.Trp1782Leu
ENST00000684676.1:c.5345G>T	ENSP00000506948.1:p.Trp1782Leu
ENST00000261866.12:c.5345G>T MANE Select	ENSP00000261866.7:p.Trp1782Leu
ENST00000261866.11:c.5345G>T	ENSP00000261866.7:p.Trp1782Leu
ENST00000427534.6:c.5345G>T	ENSP00000396110.2:p.Trp1782Leu
ENST00000535302.6:c.5345G>T	ENSP00000445278.2:p.Trp1782Leu
ENST00000558319.5:c.5345G>T	ENSP00000453599.1:p.Trp1782Leu
ENST00000558790.5:n.782G>T
ENST00000559511.5:c.193G>T
ENST00000559822.1:c.117G>T
NM_001160227.1:c.5345G>T	NP_001153699.1:p.Trp1782Leu
NM_025137.3:c.5345G>T	NP_079413.3:p.Trp1782Leu
XM_005254695.3:c.5087G>T	XP_005254752.1:p.Trp1696Leu
XM_006720700.1:c.5201G>T	XP_006720763.1:p.Trp1734Leu
XM_017022634.1:c.5345G>T	XP_016878123.1:p.Trp1782Leu
XM_017022636.1:c.2222G>T	XP_016878125.1:p.Trp741Leu
XR_931917.2:n.5399G>T
NM_025137.4:c.5345G>T MANE Select	NP_079413.3:p.Trp1782Leu
NM_001160227.2:c.5345G>T	NP_001153699.1:p.Trp1782Leu