Canonical Allele Identifier: CA470800073

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552956T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793199T>A , CM000672.2:g.93793199T>A	GRCh38
NC_000010.10:g.95552956T>A , CM000672.1:g.95552956T>A	GRCh37
NC_000010.9:g.95542946T>A	NCBI36
NG_011832.1:g.40391T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.687T>A MANE Select	ENSP00000360472.4:p.Ser229=
ENST00000485458.3:n.4663T>A
ENST00000635953.1:c.687T>A	ENSP00000490058.1:p.Ser229=
ENST00000636155.1:c.687T>A	ENSP00000490355.1:p.Ser229=
ENST00000636232.1:c.*473T>A	ENSP00000490325.1:n.*473T>A
ENST00000636754.1:c.*529T>A	ENSP00000489781.1:n.*529T>A
ENST00000636946.1:c.*856T>A	ENSP00000490654.1:n.*856T>A
ENST00000637037.1:c.*277T>A	ENSP00000490860.1:n.*277T>A
ENST00000637347.1:n.548T>A
ENST00000637611.1:c.*243T>A	ENSP00000489682.1:n.*243T>A
ENST00000637689.1:c.-685T>A	ENSP00000490496.1:n.-685T>A
ENST00000637925.1:c.*282T>A	ENSP00000489763.1:n.*282T>A
ENST00000638049.1:c.*445T>A	ENSP00000490597.1:n.*445T>A
ENST00000676175.1:n.2426T>A
ENST00000371413.4:c.687T>A	ENSP00000360467.3:p.Ser229=
ENST00000371418.8:c.687T>A	ENSP00000360472.4:p.Ser229=
ENST00000626307.1:n.4602T>A
ENST00000626946.1:n.357T>A
ENST00000627420.2:c.*396T>A	ENSP00000487116.1:n.*396T>A
ENST00000629035.2:c.615T>A	ENSP00000486908.1:p.Ser205=
ENST00000630047.2:c.543T>A	ENSP00000485917.1:p.Ser181=
ENST00000630412.1:n.475T>A
ENST00000630487.2:c.*477T>A	ENSP00000486859.1:n.*477T>A
NM_001308275.1:c.687T>A	NP_001295204.1:p.Ser229=
NM_001308276.1:c.543T>A	NP_001295205.1:p.Ser181=
NM_005097.2:c.687T>A	NP_005088.1:p.Ser229=
NM_005097.3:c.687T>A	NP_005088.1:p.Ser229=
NR_131777.1:n.951T>A
XM_017016911.2:c.687T>A	XP_016872400.1:p.Ser229=
XM_017016912.2:c.543T>A	XP_016872401.1:p.Ser181=
NM_005097.4:c.687T>A MANE Select	NP_005088.1:p.Ser229=
NM_001308275.2:c.687T>A	NP_001295204.1:p.Ser229=
NM_001308276.2:c.543T>A	NP_001295205.1:p.Ser181=
NR_131777.2:n.824T>A