Canonical Allele Identifier: CA1928771014
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793348C= , CM000672.2:g.93793348C= GRCh38
NC_000010.10:g.95553105C= , CM000672.1:g.95553105C= GRCh37
NC_000010.9:g.95543095C= NCBI36
NG_011832.1:g.40540C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.836C= MANE Select ENSP00000360472.4:p.Thr279=
ENST00000485458.3:n.4812C=
ENST00000635953.1:c.836C= ENSP00000490058.1:p.Thr279=
ENST00000636155.1:c.836C= ENSP00000490355.1:p.Thr279=
ENST00000636232.1:c.*622C= ENSP00000490325.1:n.*622C=
ENST00000636754.1:c.*678C= ENSP00000489781.1:n.*678C=
ENST00000636946.1:c.*1005C= ENSP00000490654.1:n.*1005C=
ENST00000637037.1:c.*426C= ENSP00000490860.1:n.*426C=
ENST00000637347.1:n.697C=
ENST00000637611.1:c.*392C= ENSP00000489682.1:n.*392C=
ENST00000637689.1:c.-536C= ENSP00000490496.1:n.-536C=
ENST00000637925.1:c.*431C= ENSP00000489763.1:n.*431C=
ENST00000638049.1:c.*594C= ENSP00000490597.1:n.*594C=
ENST00000676175.1:n.2575C=
ENST00000371413.4:c.836C= ENSP00000360467.3:p.Thr279=
ENST00000371418.8:c.836C= ENSP00000360472.4:p.Thr279=
ENST00000626307.1:n.4751C=
ENST00000626946.1:n.506C=
ENST00000627420.2:c.*545C= ENSP00000487116.1:n.*545C=
ENST00000629035.2:c.764C= ENSP00000486908.1:p.Thr255=
ENST00000630047.2:c.692C= ENSP00000485917.1:p.Thr231=
NM_001308275.1:c.836C= NP_001295204.1:p.Thr279=
NM_001308276.1:c.692C= NP_001295205.1:p.Thr231=
NM_005097.2:c.836C= NP_005088.1:p.Thr279=
NM_005097.3:c.836C= NP_005088.1:p.Thr279=
NR_131777.1:n.1100C=
XM_017016911.2:c.836C= XP_016872400.1:p.Thr279=
XM_017016912.2:c.692C= XP_016872401.1:p.Thr231=
NM_005097.4:c.836C= MANE Select NP_005088.1:p.Thr279=
NM_001308275.2:c.836C= NP_001295204.1:p.Thr279=
NM_001308276.2:c.692C= NP_001295205.1:p.Thr231=
NR_131777.2:n.973C=