Canonical Allele Identifier: CA377624009

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552975T>A (hg19) ; chr10:g.93793218T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793218T>A , CM000672.2:g.93793218T>A	GRCh38
NC_000010.10:g.95552975T>A , CM000672.1:g.95552975T>A	GRCh37
NC_000010.9:g.95542965T>A	NCBI36
NG_011832.1:g.40410T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.706T>A MANE Select	ENSP00000360472.4:p.Ser236Thr
ENST00000485458.3:n.4682T>A
ENST00000635953.1:c.706T>A	ENSP00000490058.1:p.Ser236Thr
ENST00000636155.1:c.706T>A	ENSP00000490355.1:p.Ser236Thr
ENST00000636232.1:c.*492T>A	ENSP00000490325.1:n.*492T>A
ENST00000636754.1:c.*548T>A	ENSP00000489781.1:n.*548T>A
ENST00000636946.1:c.*875T>A	ENSP00000490654.1:n.*875T>A
ENST00000637037.1:c.*296T>A	ENSP00000490860.1:n.*296T>A
ENST00000637347.1:n.567T>A
ENST00000637611.1:c.*262T>A	ENSP00000489682.1:n.*262T>A
ENST00000637689.1:c.-666T>A	ENSP00000490496.1:n.-666T>A
ENST00000637925.1:c.*301T>A	ENSP00000489763.1:n.*301T>A
ENST00000638049.1:c.*464T>A	ENSP00000490597.1:n.*464T>A
ENST00000676175.1:n.2445T>A
ENST00000371413.4:c.706T>A	ENSP00000360467.3:p.Ser236Thr
ENST00000371418.8:c.706T>A	ENSP00000360472.4:p.Ser236Thr
ENST00000626307.1:n.4621T>A
ENST00000626946.1:n.376T>A
ENST00000627420.2:c.*415T>A	ENSP00000487116.1:n.*415T>A
ENST00000629035.2:c.634T>A	ENSP00000486908.1:p.Ser212Thr
ENST00000630047.2:c.562T>A	ENSP00000485917.1:p.Ser188Thr
ENST00000630412.1:n.494T>A
ENST00000630487.2:c.*496T>A	ENSP00000486859.1:n.*496T>A
NM_001308275.1:c.706T>A	NP_001295204.1:p.Ser236Thr
NM_001308276.1:c.562T>A	NP_001295205.1:p.Ser188Thr
NM_005097.2:c.706T>A	NP_005088.1:p.Ser236Thr
NM_005097.3:c.706T>A	NP_005088.1:p.Ser236Thr
NR_131777.1:n.970T>A
XM_017016911.2:c.706T>A	XP_016872400.1:p.Ser236Thr
XM_017016912.2:c.562T>A	XP_016872401.1:p.Ser188Thr
NM_005097.4:c.706T>A MANE Select	NP_005088.1:p.Ser236Thr
NM_001308275.2:c.706T>A	NP_001295204.1:p.Ser236Thr
NM_001308276.2:c.562T>A	NP_001295205.1:p.Ser188Thr
NR_131777.2:n.843T>A