Canonical Allele Identifier: CA377623985

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552970A>G (hg19) ; chr10:g.93793213A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793213A>G , CM000672.2:g.93793213A>G	GRCh38
NC_000010.10:g.95552970A>G , CM000672.1:g.95552970A>G	GRCh37
NC_000010.9:g.95542960A>G	NCBI36
NG_011832.1:g.40405A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.701A>G MANE Select	ENSP00000360472.4:p.Tyr234Cys
ENST00000485458.3:n.4677A>G
ENST00000635953.1:c.701A>G	ENSP00000490058.1:p.Tyr234Cys
ENST00000636155.1:c.701A>G	ENSP00000490355.1:p.Tyr234Cys
ENST00000636232.1:c.*487A>G	ENSP00000490325.1:n.*487A>G
ENST00000636754.1:c.*543A>G	ENSP00000489781.1:n.*543A>G
ENST00000636946.1:c.*870A>G	ENSP00000490654.1:n.*870A>G
ENST00000637037.1:c.*291A>G	ENSP00000490860.1:n.*291A>G
ENST00000637347.1:n.562A>G
ENST00000637611.1:c.*257A>G	ENSP00000489682.1:n.*257A>G
ENST00000637689.1:c.-671A>G	ENSP00000490496.1:n.-671A>G
ENST00000637925.1:c.*296A>G	ENSP00000489763.1:n.*296A>G
ENST00000638049.1:c.*459A>G	ENSP00000490597.1:n.*459A>G
ENST00000676175.1:n.2440A>G
ENST00000371413.4:c.701A>G	ENSP00000360467.3:p.Tyr234Cys
ENST00000371418.8:c.701A>G	ENSP00000360472.4:p.Tyr234Cys
ENST00000626307.1:n.4616A>G
ENST00000626946.1:n.371A>G
ENST00000627420.2:c.*410A>G	ENSP00000487116.1:n.*410A>G
ENST00000629035.2:c.629A>G	ENSP00000486908.1:p.Tyr210Cys
ENST00000630047.2:c.557A>G	ENSP00000485917.1:p.Tyr186Cys
ENST00000630412.1:n.489A>G
ENST00000630487.2:c.*491A>G	ENSP00000486859.1:n.*491A>G
NM_001308275.1:c.701A>G	NP_001295204.1:p.Tyr234Cys
NM_001308276.1:c.557A>G	NP_001295205.1:p.Tyr186Cys
NM_005097.2:c.701A>G	NP_005088.1:p.Tyr234Cys
NM_005097.3:c.701A>G	NP_005088.1:p.Tyr234Cys
NR_131777.1:n.965A>G
XM_017016911.2:c.701A>G	XP_016872400.1:p.Tyr234Cys
XM_017016912.2:c.557A>G	XP_016872401.1:p.Tyr186Cys
NM_005097.4:c.701A>G MANE Select	NP_005088.1:p.Tyr234Cys
NM_001308275.2:c.701A>G	NP_001295204.1:p.Tyr234Cys
NM_001308276.2:c.557A>G	NP_001295205.1:p.Tyr186Cys
NR_131777.2:n.838A>G