Canonical Allele Identifier: CA1928774712
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93797277A= , CM000672.2:g.93797277A= GRCh38
NC_000010.10:g.95557034A= , CM000672.1:g.95557034A= GRCh37
NC_000010.9:g.95547024A= NCBI36
NG_011832.1:g.44469A=

Transcript Alleles

HGVS Amino-acid Change
NM_005097.4:c.1148A= MANE Select NP_005088.1:p.Glu383=
ENST00000371418.9:c.1148A= MANE Select ENSP00000360472.4:p.Glu383=
NM_001308275.1:c.839-472A= NP_001295204.1:n.839-472A=
NM_001308275.2:c.839-472A= NP_001295204.1:n.839-472A=
NM_001308276.1:c.1004A= NP_001295205.1:p.Glu335=
NM_001308276.2:c.1004A= NP_001295205.1:p.Glu335=
NM_005097.2:c.1148A= NP_005088.1:p.Glu383=
NM_005097.3:c.1148A= NP_005088.1:p.Glu383=
NR_131777.1:n.1412A=
NR_131777.2:n.1285A=
ENST00000371413.4:c.839-472A= ENSP00000360467.3:n.839-472A=
ENST00000371418.8:c.1148A= ENSP00000360472.4:p.Glu383=
ENST00000485458.3:n.5124A=
ENST00000626307.1:n.5063A=
ENST00000627420.2:c.*857A= ENSP00000487116.1:n.*857A=
ENST00000629035.2:c.1076A= ENSP00000486908.1:p.Glu359=
ENST00000630047.2:c.1004A= ENSP00000485917.1:p.Glu335=
ENST00000635804.1:n.582A=
ENST00000635953.1:c.*570A= ENSP00000490058.1:n.*570A=
ENST00000636155.1:c.838+3927A= ENSP00000490355.1:n.838+3927A=
ENST00000636232.1:c.*934A= ENSP00000490325.1:n.*934A=
ENST00000636754.1:c.*990A= ENSP00000489781.1:n.*990A=
ENST00000636946.1:c.*1008-472A= ENSP00000490654.1:n.*1008-472A=
ENST00000637037.1:c.*738A= ENSP00000490860.1:n.*738A=
ENST00000637347.1:n.1009A=
ENST00000637611.1:c.*704A= ENSP00000489682.1:n.*704A=
ENST00000637689.1:c.-224A= ENSP00000490496.1:n.-224A=
ENST00000637925.1:c.*743A= ENSP00000489763.1:n.*743A=
ENST00000638049.1:c.*906A= ENSP00000490597.1:n.*906A=
ENST00000676175.1:n.2887A=
XM_017016912.2:c.695-472A= XP_016872401.1:n.695-472A=