Canonical Allele Identifier: CA377628194

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557078C>T (hg19) ; chr10:g.93797321C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797321C>T , CM000672.2:g.93797321C>T	GRCh38
NC_000010.10:g.95557078C>T , CM000672.1:g.95557078C>T	GRCh37
NC_000010.9:g.95547068C>T	NCBI36
NG_011832.1:g.44513C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1192C>T MANE Select	ENSP00000360472.4:p.His398Tyr
ENST00000485458.3:n.5168C>T
ENST00000635804.1:n.626C>T
ENST00000635953.1:c.*614C>T	ENSP00000490058.1:n.*614C>T
ENST00000636155.1:c.838+3971C>T	ENSP00000490355.1:n.838+3971C>T
ENST00000636232.1:c.*978C>T	ENSP00000490325.1:n.*978C>T
ENST00000636754.1:c.*1034C>T	ENSP00000489781.1:n.*1034C>T
ENST00000636946.1:c.*1008-428C>T	ENSP00000490654.1:n.*1008-428C>T
ENST00000637037.1:c.*782C>T	ENSP00000490860.1:n.*782C>T
ENST00000637347.1:n.1053C>T
ENST00000637611.1:c.*748C>T	ENSP00000489682.1:n.*748C>T
ENST00000637689.1:c.-180C>T	ENSP00000490496.1:n.-180C>T
ENST00000637925.1:c.*787C>T	ENSP00000489763.1:n.*787C>T
ENST00000638049.1:c.*950C>T	ENSP00000490597.1:n.*950C>T
ENST00000676175.1:n.2931C>T
ENST00000371413.4:c.839-428C>T	ENSP00000360467.3:n.839-428C>T
ENST00000371418.8:c.1192C>T	ENSP00000360472.4:p.His398Tyr
ENST00000626307.1:n.5107C>T
ENST00000627420.2:c.*901C>T	ENSP00000487116.1:n.*901C>T
ENST00000629035.2:c.1120C>T	ENSP00000486908.1:p.His374Tyr
ENST00000630047.2:c.1048C>T	ENSP00000485917.1:p.His350Tyr
NM_001308275.1:c.839-428C>T	NP_001295204.1:n.839-428C>T
NM_001308276.1:c.1048C>T	NP_001295205.1:p.His350Tyr
NM_005097.2:c.1192C>T	NP_005088.1:p.His398Tyr
NM_005097.3:c.1192C>T	NP_005088.1:p.His398Tyr
NR_131777.1:n.1456C>T
XM_017016912.2:c.695-428C>T	XP_016872401.1:n.695-428C>T
NM_005097.4:c.1192C>T MANE Select	NP_005088.1:p.His398Tyr
NM_001308275.2:c.839-428C>T	NP_001295204.1:n.839-428C>T
NM_001308276.2:c.1048C>T	NP_001295205.1:p.His350Tyr
NR_131777.2:n.1329C>T