Canonical Allele Identifier: CA377623934

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552958A>G (hg19) ; chr10:g.93793201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793201A>G , CM000672.2:g.93793201A>G	GRCh38
NC_000010.10:g.95552958A>G , CM000672.1:g.95552958A>G	GRCh37
NC_000010.9:g.95542948A>G	NCBI36
NG_011832.1:g.40393A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.689A>G MANE Select	ENSP00000360472.4:p.Gln230Arg
ENST00000485458.3:n.4665A>G
ENST00000635953.1:c.689A>G	ENSP00000490058.1:p.Gln230Arg
ENST00000636155.1:c.689A>G	ENSP00000490355.1:p.Gln230Arg
ENST00000636232.1:c.*475A>G	ENSP00000490325.1:n.*475A>G
ENST00000636754.1:c.*531A>G	ENSP00000489781.1:n.*531A>G
ENST00000636946.1:c.*858A>G	ENSP00000490654.1:n.*858A>G
ENST00000637037.1:c.*279A>G	ENSP00000490860.1:n.*279A>G
ENST00000637347.1:n.550A>G
ENST00000637611.1:c.*245A>G	ENSP00000489682.1:n.*245A>G
ENST00000637689.1:c.-683A>G	ENSP00000490496.1:n.-683A>G
ENST00000637925.1:c.*284A>G	ENSP00000489763.1:n.*284A>G
ENST00000638049.1:c.*447A>G	ENSP00000490597.1:n.*447A>G
ENST00000676175.1:n.2428A>G
ENST00000371413.4:c.689A>G	ENSP00000360467.3:p.Gln230Arg
ENST00000371418.8:c.689A>G	ENSP00000360472.4:p.Gln230Arg
ENST00000626307.1:n.4604A>G
ENST00000626946.1:n.359A>G
ENST00000627420.2:c.*398A>G	ENSP00000487116.1:n.*398A>G
ENST00000629035.2:c.617A>G	ENSP00000486908.1:p.Gln206Arg
ENST00000630047.2:c.545A>G	ENSP00000485917.1:p.Gln182Arg
ENST00000630412.1:n.477A>G
ENST00000630487.2:c.*479A>G	ENSP00000486859.1:n.*479A>G
NM_001308275.1:c.689A>G	NP_001295204.1:p.Gln230Arg
NM_001308276.1:c.545A>G	NP_001295205.1:p.Gln182Arg
NM_005097.2:c.689A>G	NP_005088.1:p.Gln230Arg
NM_005097.3:c.689A>G	NP_005088.1:p.Gln230Arg
NR_131777.1:n.953A>G
XM_017016911.2:c.689A>G	XP_016872400.1:p.Gln230Arg
XM_017016912.2:c.545A>G	XP_016872401.1:p.Gln182Arg
NM_005097.4:c.689A>G MANE Select	NP_005088.1:p.Gln230Arg
NM_001308275.2:c.689A>G	NP_001295204.1:p.Gln230Arg
NM_001308276.2:c.545A>G	NP_001295205.1:p.Gln182Arg
NR_131777.2:n.826A>G