Canonical Allele Identifier: CA2789043590

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793479_93793480del , CM000672.2:g.93793479_93793480del	GRCh38
NC_000010.10:g.95553236_95553237del , CM000672.1:g.95553236_95553237del	GRCh37
NC_000010.9:g.95543226_95543227del	NCBI36
NG_011832.1:g.40671_40672del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+129_838+130del MANE Select	ENSP00000360472.4:n.838+129_838+130del
ENST00000485458.3:n.4814+129_4814+130del
ENST00000635953.1:c.838+129_838+130del	ENSP00000490058.1:n.838+129_838+130del
ENST00000636155.1:c.838+129_838+130del	ENSP00000490355.1:n.838+129_838+130del
ENST00000636232.1:c.*624+129_*624+130del	ENSP00000490325.1:n.*624+129_*624+130del
ENST00000636754.1:c.*680+129_*680+130del	ENSP00000489781.1:n.*680+129_*680+130del
ENST00000636946.1:c.*1007+129_*1007+130del	ENSP00000490654.1:n.*1007+129_*1007+130del
ENST00000637037.1:c.*428+129_*428+130del	ENSP00000490860.1:n.*428+129_*428+130del
ENST00000637347.1:n.699+129_699+130del
ENST00000637611.1:c.*394+129_*394+130del	ENSP00000489682.1:n.*394+129_*394+130del
ENST00000637689.1:c.-534+129_-534+130del	ENSP00000490496.1:n.-534+129_-534+130del
ENST00000637925.1:c.*433+129_*433+130del	ENSP00000489763.1:n.*433+129_*433+130del
ENST00000638049.1:c.*596+129_*596+130del	ENSP00000490597.1:n.*596+129_*596+130del
ENST00000676175.1:n.2577+129_2577+130del
ENST00000371413.4:c.838+129_838+130del	ENSP00000360467.3:n.838+129_838+130del
ENST00000371418.8:c.838+129_838+130del	ENSP00000360472.4:n.838+129_838+130del
ENST00000626307.1:n.4753+129_4753+130del
ENST00000626946.1:n.508+129_508+130del
ENST00000627420.2:c.*547+129_*547+130del	ENSP00000487116.1:n.*547+129_*547+130del
ENST00000629035.2:c.766+129_766+130del	ENSP00000486908.1:n.766+129_766+130del
ENST00000630047.2:c.694+129_694+130del	ENSP00000485917.1:n.694+129_694+130del
NM_001308275.1:c.838+129_838+130del	NP_001295204.1:n.838+129_838+130del
NM_001308276.1:c.694+129_694+130del	NP_001295205.1:n.694+129_694+130del
NM_005097.2:c.838+129_838+130del	NP_005088.1:n.838+129_838+130del
NM_005097.3:c.838+129_838+130del	NP_005088.1:n.838+129_838+130del
NR_131777.1:n.1102+129_1102+130del
XM_017016911.2:c.838+129_838+130del	XP_016872400.1:n.838+129_838+130del
XM_017016912.2:c.694+129_694+130del	XP_016872401.1:n.694+129_694+130del
NM_005097.4:c.838+129_838+130del MANE Select	NP_005088.1:n.838+129_838+130del
NM_001308275.2:c.838+129_838+130del	NP_001295204.1:n.838+129_838+130del
NM_001308276.2:c.694+129_694+130del	NP_001295205.1:n.694+129_694+130del
NR_131777.2:n.975+129_975+130del