Canonical Allele Identifier: CA1928771112

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793445_93793446delinsAT , CM000672.2:g.93793445_93793446delinsAT	GRCh38
NC_000010.10:g.95553202_95553203delinsAT , CM000672.1:g.95553202_95553203delinsAT	GRCh37
NC_000010.9:g.95543192_95543193delinsAT	NCBI36
NG_011832.1:g.40637_40638delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+95_838+96delinsAT MANE Select	ENSP00000360472.4:n.838+95_838+96delinsAT
ENST00000485458.3:n.4814+95_4814+96delinsAT
ENST00000635953.1:c.838+95_838+96delinsAT	ENSP00000490058.1:n.838+95_838+96delinsAT
ENST00000636155.1:c.838+95_838+96delinsAT	ENSP00000490355.1:n.838+95_838+96delinsAT
ENST00000636232.1:c.*624+95_*624+96delinsAT	ENSP00000490325.1:n.*624+95_*624+96delinsAT
ENST00000636754.1:c.*680+95_*680+96delinsAT	ENSP00000489781.1:n.*680+95_*680+96delinsAT
ENST00000636946.1:c.*1007+95_*1007+96delinsAT	ENSP00000490654.1:n.*1007+95_*1007+96delinsAT
ENST00000637037.1:c.*428+95_*428+96delinsAT	ENSP00000490860.1:n.*428+95_*428+96delinsAT
ENST00000637347.1:n.699+95_699+96delinsAT
ENST00000637611.1:c.*394+95_*394+96delinsAT	ENSP00000489682.1:n.*394+95_*394+96delinsAT
ENST00000637689.1:c.-534+95_-534+96delinsAT	ENSP00000490496.1:n.-534+95_-534+96delinsAT
ENST00000637925.1:c.*433+95_*433+96delinsAT	ENSP00000489763.1:n.*433+95_*433+96delinsAT
ENST00000638049.1:c.*596+95_*596+96delinsAT	ENSP00000490597.1:n.*596+95_*596+96delinsAT
ENST00000676175.1:n.2577+95_2577+96delinsAT
ENST00000371413.4:c.838+95_838+96delinsAT	ENSP00000360467.3:n.838+95_838+96delinsAT
ENST00000371418.8:c.838+95_838+96delinsAT	ENSP00000360472.4:n.838+95_838+96delinsAT
ENST00000626307.1:n.4753+95_4753+96delinsAT
ENST00000626946.1:n.508+95_508+96delinsAT
ENST00000627420.2:c.*547+95_*547+96delinsAT	ENSP00000487116.1:n.*547+95_*547+96delinsAT
ENST00000629035.2:c.766+95_766+96delinsAT	ENSP00000486908.1:n.766+95_766+96delinsAT
ENST00000630047.2:c.694+95_694+96delinsAT	ENSP00000485917.1:n.694+95_694+96delinsAT
NM_001308275.1:c.838+95_838+96delinsAT	NP_001295204.1:n.838+95_838+96delinsAT
NM_001308276.1:c.694+95_694+96delinsAT	NP_001295205.1:n.694+95_694+96delinsAT
NM_005097.2:c.838+95_838+96delinsAT	NP_005088.1:n.838+95_838+96delinsAT
NM_005097.3:c.838+95_838+96delinsAT	NP_005088.1:n.838+95_838+96delinsAT
NR_131777.1:n.1102+95_1102+96delinsAT
XM_017016911.2:c.838+95_838+96delinsAT	XP_016872400.1:n.838+95_838+96delinsAT
XM_017016912.2:c.694+95_694+96delinsAT	XP_016872401.1:n.694+95_694+96delinsAT
NM_005097.4:c.838+95_838+96delinsAT MANE Select	NP_005088.1:n.838+95_838+96delinsAT
NM_001308275.2:c.838+95_838+96delinsAT	NP_001295204.1:n.838+95_838+96delinsAT
NM_001308276.2:c.694+95_694+96delinsAT	NP_001295205.1:n.694+95_694+96delinsAT
NR_131777.2:n.975+95_975+96delinsAT