Canonical Allele Identifier: CA1928787642

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793269_93793270delinsGC , CM000672.2:g.93793269_93793270delinsGC	GRCh38
NC_000010.10:g.95553026_95553027delinsGC , CM000672.1:g.95553026_95553027delinsGC	GRCh37
NC_000010.9:g.95543016_95543017delinsGC	NCBI36
NG_011832.1:g.40461_40462delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.757_758delinsGC MANE Select	ENSP00000360472.4:p.Ala253=
ENST00000485458.3:n.4733_4734delinsGC
ENST00000635953.1:c.757_758delinsGC	ENSP00000490058.1:p.Ala253=
ENST00000636155.1:c.757_758delinsGC	ENSP00000490355.1:p.Ala253=
ENST00000636232.1:c.*543_*544delinsGC	ENSP00000490325.1:n.*543_*544delinsGC
ENST00000636754.1:c.*599_*600delinsGC	ENSP00000489781.1:n.*599_*600delinsGC
ENST00000636946.1:c.*926_*927delinsGC	ENSP00000490654.1:n.*926_*927delinsGC
ENST00000637037.1:c.*347_*348delinsGC	ENSP00000490860.1:n.*347_*348delinsGC
ENST00000637347.1:n.618_619delinsGC
ENST00000637611.1:c.*313_*314delinsGC	ENSP00000489682.1:n.*313_*314delinsGC
ENST00000637689.1:c.-615_-614delinsGC	ENSP00000490496.1:n.-615_-614delinsGC
ENST00000637925.1:c.*352_*353delinsGC	ENSP00000489763.1:n.*352_*353delinsGC
ENST00000638049.1:c.*515_*516delinsGC	ENSP00000490597.1:n.*515_*516delinsGC
ENST00000676175.1:n.2496_2497delinsGC
ENST00000371413.4:c.757_758delinsGC	ENSP00000360467.3:p.Ala253=
ENST00000371418.8:c.757_758delinsGC	ENSP00000360472.4:p.Ala253=
ENST00000626307.1:n.4672_4673delinsGC
ENST00000626946.1:n.427_428delinsGC
ENST00000627420.2:c.*466_*467delinsGC	ENSP00000487116.1:n.*466_*467delinsGC
ENST00000629035.2:c.685_686delinsGC	ENSP00000486908.1:p.Ala229=
ENST00000630047.2:c.613_614delinsGC	ENSP00000485917.1:p.Ala205=
ENST00000630412.1:n.545_546delinsGC
ENST00000630487.2:c.*547_*548delinsGC	ENSP00000486859.1:n.*547_*548delinsGC
NM_001308275.1:c.757_758delinsGC	NP_001295204.1:p.Ala253=
NM_001308276.1:c.613_614delinsGC	NP_001295205.1:p.Ala205=
NM_005097.2:c.757_758delinsGC	NP_005088.1:p.Ala253=
NM_005097.3:c.757_758delinsGC	NP_005088.1:p.Ala253=
NR_131777.1:n.1021_1022delinsGC
XM_017016911.2:c.757_758delinsGC	XP_016872400.1:p.Ala253=
XM_017016912.2:c.613_614delinsGC	XP_016872401.1:p.Ala205=
NM_005097.4:c.757_758delinsGC MANE Select	NP_005088.1:p.Ala253=
NM_001308275.2:c.757_758delinsGC	NP_001295204.1:p.Ala253=
NM_001308276.2:c.613_614delinsGC	NP_001295205.1:p.Ala205=
NR_131777.2:n.894_895delinsGC