Canonical Allele Identifier: CA1928787538
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793196G= , CM000672.2:g.93793196G= GRCh38
NC_000010.10:g.95552953G= , CM000672.1:g.95552953G= GRCh37
NC_000010.9:g.95542943G= NCBI36
NG_011832.1:g.40388G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.684G= MANE Select ENSP00000360472.4:p.Lys228=
ENST00000485458.3:n.4660G=
ENST00000635953.1:c.684G= ENSP00000490058.1:p.Lys228=
ENST00000636155.1:c.684G= ENSP00000490355.1:p.Lys228=
ENST00000636232.1:c.*470G= ENSP00000490325.1:n.*470G=
ENST00000636754.1:c.*526G= ENSP00000489781.1:n.*526G=
ENST00000636946.1:c.*853G= ENSP00000490654.1:n.*853G=
ENST00000637037.1:c.*274G= ENSP00000490860.1:n.*274G=
ENST00000637347.1:n.545G=
ENST00000637611.1:c.*240G= ENSP00000489682.1:n.*240G=
ENST00000637689.1:c.-688G= ENSP00000490496.1:n.-688G=
ENST00000637925.1:c.*279G= ENSP00000489763.1:n.*279G=
ENST00000638049.1:c.*442G= ENSP00000490597.1:n.*442G=
ENST00000676175.1:n.2423G=
ENST00000371413.4:c.684G= ENSP00000360467.3:p.Lys228=
ENST00000371418.8:c.684G= ENSP00000360472.4:p.Lys228=
ENST00000626307.1:n.4599G=
ENST00000626946.1:n.354G=
ENST00000627420.2:c.*393G= ENSP00000487116.1:n.*393G=
ENST00000629035.2:c.612G= ENSP00000486908.1:p.Lys204=
ENST00000630047.2:c.540G= ENSP00000485917.1:p.Lys180=
ENST00000630412.1:n.472G=
ENST00000630487.2:c.*474G= ENSP00000486859.1:n.*474G=
NM_001308275.1:c.684G= NP_001295204.1:p.Lys228=
NM_001308276.1:c.540G= NP_001295205.1:p.Lys180=
NM_005097.2:c.684G= NP_005088.1:p.Lys228=
NM_005097.3:c.684G= NP_005088.1:p.Lys228=
NR_131777.1:n.948G=
XM_017016911.2:c.684G= XP_016872400.1:p.Lys228=
XM_017016912.2:c.540G= XP_016872401.1:p.Lys180=
NM_005097.4:c.684G= MANE Select NP_005088.1:p.Lys228=
NM_001308275.2:c.684G= NP_001295204.1:p.Lys228=
NM_001308276.2:c.540G= NP_001295205.1:p.Lys180=
NR_131777.2:n.821G=