Canonical Allele Identifier: CA490329524

Gene: SPG11

Linked Data

• MyVariant Identifiers: chr15:g.44876091T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44583893T>C , CM000677.2:g.44583893T>C	GRCh38
NC_000015.9:g.44876091T>C , CM000677.1:g.44876091T>C	GRCh37
NC_000015.8:g.42663383T>C	NCBI36
NG_008885.1:g.84786A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000559511.6:c.5787A>G	ENSP00000453246.2:p.Pro1929=
ENST00000561391.2:n.2015A>G
ENST00000682065.1:c.5643A>G	ENSP00000507025.1:p.Pro1881=
ENST00000682460.1:c.*2044A>G	ENSP00000508334.1:n.*2044A>G
ENST00000682495.1:c.*2279A>G	ENSP00000507166.1:n.*2279A>G
ENST00000682669.1:c.5586A>G	ENSP00000507782.1:p.Pro1862=
ENST00000683186.1:c.*2550A>G	ENSP00000507268.1:n.*2550A>G
ENST00000683496.1:c.5787A>G	ENSP00000506968.1:p.Pro1929=
ENST00000683734.1:c.5787A>G	ENSP00000508319.1:p.Pro1929=
ENST00000683753.1:n.4833A>G
ENST00000684038.1:c.*2207A>G	ENSP00000507141.1:n.*2207A>G
ENST00000684235.1:c.5787A>G	ENSP00000508295.1:p.Pro1929=
ENST00000684676.1:c.5558A>G	ENSP00000506948.1:p.Gln1853Arg
ENST00000261866.12:c.5787A>G MANE Select	ENSP00000261866.7:p.Pro1929=
ENST00000261866.11:c.5787A>G	ENSP00000261866.7:p.Pro1929=
ENST00000427534.6:c.5787A>G	ENSP00000396110.2:p.Pro1929=
ENST00000535302.6:c.5787A>G	ENSP00000445278.2:p.Pro1929=
ENST00000558319.5:c.5787A>G	ENSP00000453599.1:p.Pro1929=
ENST00000559511.5:c.635A>G
ENST00000559822.1:c.330A>G
NM_001160227.1:c.5787A>G	NP_001153699.1:p.Pro1929=
NM_025137.3:c.5787A>G	NP_079413.3:p.Pro1929=
XM_005254695.3:c.5529A>G	XP_005254752.1:p.Pro1843=
XM_006720700.1:c.5643A>G	XP_006720763.1:p.Pro1881=
XM_017022634.1:c.5787A>G	XP_016878123.1:p.Pro1929=
XM_017022636.1:c.2664A>G	XP_016878125.1:p.Pro888=
NM_025137.4:c.5787A>G MANE Select	NP_079413.3:p.Pro1929=
NM_001160227.2:c.5787A>G	NP_001153699.1:p.Pro1929=