Canonical Allele Identifier: CA5611193

Gene: LGI1

Linked Data

• dbSNP Id: rs780606965
• ExAC: 10:95553137 G / GTAA
• MyVariant Identifiers: chr10:g.95553137_95553138insTAA (hg19) ; chr10:g.93793380_93793381insTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793382_93793384dup , CM000672.2:g.93793382_93793384dup	GRCh38
NC_000010.10:g.95553139_95553141dup , CM000672.1:g.95553139_95553141dup	GRCh37
NC_000010.9:g.95543129_95543131dup	NCBI36
NG_011832.1:g.40574_40576dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+32_838+34dup MANE Select	ENSP00000360472.4:n.838+32_838+34dup
ENST00000485458.3:n.4814+32_4814+34dup
ENST00000635953.1:c.838+32_838+34dup	ENSP00000490058.1:n.838+32_838+34dup
ENST00000636155.1:c.838+32_838+34dup	ENSP00000490355.1:n.838+32_838+34dup
ENST00000636232.1:c.*624+32_*624+34dup	ENSP00000490325.1:n.*624+32_*624+34dup
ENST00000636754.1:c.*680+32_*680+34dup	ENSP00000489781.1:n.*680+32_*680+34dup
ENST00000636946.1:c.*1007+32_*1007+34dup	ENSP00000490654.1:n.*1007+32_*1007+34dup
ENST00000637037.1:c.*428+32_*428+34dup	ENSP00000490860.1:n.*428+32_*428+34dup
ENST00000637347.1:n.699+32_699+34dup
ENST00000637611.1:c.*394+32_*394+34dup	ENSP00000489682.1:n.*394+32_*394+34dup
ENST00000637689.1:c.-534+32_-534+34dup	ENSP00000490496.1:n.-534+32_-534+34dup
ENST00000637925.1:c.*433+32_*433+34dup	ENSP00000489763.1:n.*433+32_*433+34dup
ENST00000638049.1:c.*596+32_*596+34dup	ENSP00000490597.1:n.*596+32_*596+34dup
ENST00000676175.1:n.2577+32_2577+34dup
ENST00000371413.4:c.838+32_838+34dup	ENSP00000360467.3:n.838+32_838+34dup
ENST00000371418.8:c.838+32_838+34dup	ENSP00000360472.4:n.838+32_838+34dup
ENST00000626307.1:n.4753+32_4753+34dup
ENST00000626946.1:n.508+32_508+34dup
ENST00000627420.2:c.*547+32_*547+34dup	ENSP00000487116.1:n.*547+32_*547+34dup
ENST00000629035.2:c.766+32_766+34dup	ENSP00000486908.1:n.766+32_766+34dup
ENST00000630047.2:c.694+32_694+34dup	ENSP00000485917.1:n.694+32_694+34dup
NM_001308275.1:c.838+32_838+34dup	NP_001295204.1:n.838+32_838+34dup
NM_001308276.1:c.694+32_694+34dup	NP_001295205.1:n.694+32_694+34dup
NM_005097.2:c.838+32_838+34dup	NP_005088.1:n.838+32_838+34dup
NM_005097.3:c.838+32_838+34dup	NP_005088.1:n.838+32_838+34dup
NR_131777.1:n.1102+32_1102+34dup
XM_017016911.2:c.838+32_838+34dup	XP_016872400.1:n.838+32_838+34dup
XM_017016912.2:c.694+32_694+34dup	XP_016872401.1:n.694+32_694+34dup
NM_005097.4:c.838+32_838+34dup MANE Select	NP_005088.1:n.838+32_838+34dup
NM_001308275.2:c.838+32_838+34dup	NP_001295204.1:n.838+32_838+34dup
NM_001308276.2:c.694+32_694+34dup	NP_001295205.1:n.694+32_694+34dup
NR_131777.2:n.975+32_975+34dup