Canonical Allele Identifier: CA377627171

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556916T>C (hg19) ; chr10:g.93797159T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797159T>C , CM000672.2:g.93797159T>C	GRCh38
NC_000010.10:g.95556916T>C , CM000672.1:g.95556916T>C	GRCh37
NC_000010.9:g.95546906T>C	NCBI36
NG_011832.1:g.44351T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1030T>C MANE Select	ENSP00000360472.4:p.Trp344Arg
ENST00000485458.3:n.5006T>C
ENST00000635804.1:n.464T>C
ENST00000635953.1:c.*452T>C	ENSP00000490058.1:n.*452T>C
ENST00000636155.1:c.838+3809T>C	ENSP00000490355.1:n.838+3809T>C
ENST00000636232.1:c.*816T>C	ENSP00000490325.1:n.*816T>C
ENST00000636754.1:c.*872T>C	ENSP00000489781.1:n.*872T>C
ENST00000636946.1:c.*1008-590T>C	ENSP00000490654.1:n.*1008-590T>C
ENST00000637037.1:c.*620T>C	ENSP00000490860.1:n.*620T>C
ENST00000637347.1:n.891T>C
ENST00000637611.1:c.*586T>C	ENSP00000489682.1:n.*586T>C
ENST00000637689.1:c.-342T>C	ENSP00000490496.1:n.-342T>C
ENST00000637925.1:c.*625T>C	ENSP00000489763.1:n.*625T>C
ENST00000638049.1:c.*788T>C	ENSP00000490597.1:n.*788T>C
ENST00000676175.1:n.2769T>C
ENST00000371413.4:c.839-590T>C	ENSP00000360467.3:n.839-590T>C
ENST00000371418.8:c.1030T>C	ENSP00000360472.4:p.Trp344Arg
ENST00000626307.1:n.4945T>C
ENST00000627420.2:c.*739T>C	ENSP00000487116.1:n.*739T>C
ENST00000629035.2:c.958T>C	ENSP00000486908.1:p.Trp320Arg
ENST00000630047.2:c.886T>C	ENSP00000485917.1:p.Trp296Arg
NM_001308275.1:c.839-590T>C	NP_001295204.1:n.839-590T>C
NM_001308276.1:c.886T>C	NP_001295205.1:p.Trp296Arg
NM_005097.2:c.1030T>C	NP_005088.1:p.Trp344Arg
NM_005097.3:c.1030T>C	NP_005088.1:p.Trp344Arg
NR_131777.1:n.1294T>C
XM_017016912.2:c.695-590T>C	XP_016872401.1:n.695-590T>C
NM_005097.4:c.1030T>C MANE Select	NP_005088.1:p.Trp344Arg
NM_001308275.2:c.839-590T>C	NP_001295204.1:n.839-590T>C
NM_001308276.2:c.886T>C	NP_001295205.1:p.Trp296Arg
NR_131777.2:n.1167T>C