Canonical Allele Identifier: CA1928787478
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793107T= , CM000672.2:g.93793107T= GRCh38
NC_000010.10:g.95552864T= , CM000672.1:g.95552864T= GRCh37
NC_000010.9:g.95542854T= NCBI36
NG_011832.1:g.40299T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371418.9:c.674-79T= MANE Select ENSP00000360472.4:n.674-79T=
ENST00000485458.3:n.4650-79T=
ENST00000635953.1:c.674-79T= ENSP00000490058.1:n.674-79T=
ENST00000636155.1:c.674-79T= ENSP00000490355.1:n.674-79T=
ENST00000636232.1:c.*460-79T= ENSP00000490325.1:n.*460-79T=
ENST00000636754.1:c.*516-79T= ENSP00000489781.1:n.*516-79T=
ENST00000636946.1:c.*843-79T= ENSP00000490654.1:n.*843-79T=
ENST00000637037.1:c.*264-79T= ENSP00000490860.1:n.*264-79T=
ENST00000637347.1:n.535-79T=
ENST00000637611.1:c.*230-79T= ENSP00000489682.1:n.*230-79T=
ENST00000637689.1:c.-698-79T= ENSP00000490496.1:n.-698-79T=
ENST00000637925.1:c.*269-79T= ENSP00000489763.1:n.*269-79T=
ENST00000638049.1:c.*432-79T= ENSP00000490597.1:n.*432-79T=
ENST00000676175.1:n.2413-79T=
ENST00000371413.4:c.674-79T= ENSP00000360467.3:n.674-79T=
ENST00000371418.8:c.674-79T= ENSP00000360472.4:n.674-79T=
ENST00000626307.1:n.4589-79T=
ENST00000626946.1:n.265T=
ENST00000627420.2:c.*383-79T= ENSP00000487116.1:n.*383-79T=
ENST00000629035.2:c.602-79T= ENSP00000486908.1:n.602-79T=
ENST00000630047.2:c.530-79T= ENSP00000485917.1:n.530-79T=
ENST00000630412.1:n.462-79T=
ENST00000630487.2:c.*464-79T= ENSP00000486859.1:n.*464-79T=
NM_001308275.1:c.674-79T= NP_001295204.1:n.674-79T=
NM_001308276.1:c.530-79T= NP_001295205.1:n.530-79T=
NM_005097.2:c.674-79T= NP_005088.1:n.674-79T=
NM_005097.3:c.674-79T= NP_005088.1:n.674-79T=
NR_131777.1:n.938-79T=
XM_017016911.2:c.674-79T= XP_016872400.1:n.674-79T=
XM_017016912.2:c.530-79T= XP_016872401.1:n.530-79T=
NM_005097.4:c.674-79T= MANE Select NP_005088.1:n.674-79T=
NM_001308275.2:c.674-79T= NP_001295204.1:n.674-79T=
NM_001308276.2:c.530-79T= NP_001295205.1:n.530-79T=
NR_131777.2:n.811-79T=