Canonical Allele Identifier: CA377624359

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553055C>A (hg19) ; chr10:g.93793298C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793298C>A , CM000672.2:g.93793298C>A	GRCh38
NC_000010.10:g.95553055C>A , CM000672.1:g.95553055C>A	GRCh37
NC_000010.9:g.95543045C>A	NCBI36
NG_011832.1:g.40490C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.786C>A MANE Select	ENSP00000360472.4:p.Phe262Leu
ENST00000485458.3:n.4762C>A
ENST00000635953.1:c.786C>A	ENSP00000490058.1:p.Phe262Leu
ENST00000636155.1:c.786C>A	ENSP00000490355.1:p.Phe262Leu
ENST00000636232.1:c.*572C>A	ENSP00000490325.1:n.*572C>A
ENST00000636754.1:c.*628C>A	ENSP00000489781.1:n.*628C>A
ENST00000636946.1:c.*955C>A	ENSP00000490654.1:n.*955C>A
ENST00000637037.1:c.*376C>A	ENSP00000490860.1:n.*376C>A
ENST00000637347.1:n.647C>A
ENST00000637611.1:c.*342C>A	ENSP00000489682.1:n.*342C>A
ENST00000637689.1:c.-586C>A	ENSP00000490496.1:n.-586C>A
ENST00000637925.1:c.*381C>A	ENSP00000489763.1:n.*381C>A
ENST00000638049.1:c.*544C>A	ENSP00000490597.1:n.*544C>A
ENST00000676175.1:n.2525C>A
ENST00000371413.4:c.786C>A	ENSP00000360467.3:p.Phe262Leu
ENST00000371418.8:c.786C>A	ENSP00000360472.4:p.Phe262Leu
ENST00000626307.1:n.4701C>A
ENST00000626946.1:n.456C>A
ENST00000627420.2:c.*495C>A	ENSP00000487116.1:n.*495C>A
ENST00000629035.2:c.714C>A	ENSP00000486908.1:p.Phe238Leu
ENST00000630047.2:c.642C>A	ENSP00000485917.1:p.Phe214Leu
ENST00000630487.2:c.*576C>A	ENSP00000486859.1:n.*576C>A
NM_001308275.1:c.786C>A	NP_001295204.1:p.Phe262Leu
NM_001308276.1:c.642C>A	NP_001295205.1:p.Phe214Leu
NM_005097.2:c.786C>A	NP_005088.1:p.Phe262Leu
NM_005097.3:c.786C>A	NP_005088.1:p.Phe262Leu
NR_131777.1:n.1050C>A
XM_017016911.2:c.786C>A	XP_016872400.1:p.Phe262Leu
XM_017016912.2:c.642C>A	XP_016872401.1:p.Phe214Leu
NM_005097.4:c.786C>A MANE Select	NP_005088.1:p.Phe262Leu
NM_001308275.2:c.786C>A	NP_001295204.1:p.Phe262Leu
NM_001308276.2:c.642C>A	NP_001295205.1:p.Phe214Leu
NR_131777.2:n.923C>A