Canonical Allele Identifier: CA1928787591
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793229A= , CM000672.2:g.93793229A= GRCh38
NC_000010.10:g.95552986A= , CM000672.1:g.95552986A= GRCh37
NC_000010.9:g.95542976A= NCBI36
NG_011832.1:g.40421A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.717A= MANE Select ENSP00000360472.4:p.Ile239=
ENST00000485458.3:n.4693A=
ENST00000635953.1:c.717A= ENSP00000490058.1:p.Ile239=
ENST00000636155.1:c.717A= ENSP00000490355.1:p.Ile239=
ENST00000636232.1:c.*503A= ENSP00000490325.1:n.*503A=
ENST00000636754.1:c.*559A= ENSP00000489781.1:n.*559A=
ENST00000636946.1:c.*886A= ENSP00000490654.1:n.*886A=
ENST00000637037.1:c.*307A= ENSP00000490860.1:n.*307A=
ENST00000637347.1:n.578A=
ENST00000637611.1:c.*273A= ENSP00000489682.1:n.*273A=
ENST00000637689.1:c.-655A= ENSP00000490496.1:n.-655A=
ENST00000637925.1:c.*312A= ENSP00000489763.1:n.*312A=
ENST00000638049.1:c.*475A= ENSP00000490597.1:n.*475A=
ENST00000676175.1:n.2456A=
ENST00000371413.4:c.717A= ENSP00000360467.3:p.Ile239=
ENST00000371418.8:c.717A= ENSP00000360472.4:p.Ile239=
ENST00000626307.1:n.4632A=
ENST00000626946.1:n.387A=
ENST00000627420.2:c.*426A= ENSP00000487116.1:n.*426A=
ENST00000629035.2:c.645A= ENSP00000486908.1:p.Ile215=
ENST00000630047.2:c.573A= ENSP00000485917.1:p.Ile191=
ENST00000630412.1:n.505A=
ENST00000630487.2:c.*507A= ENSP00000486859.1:n.*507A=
NM_001308275.1:c.717A= NP_001295204.1:p.Ile239=
NM_001308276.1:c.573A= NP_001295205.1:p.Ile191=
NM_005097.2:c.717A= NP_005088.1:p.Ile239=
NM_005097.3:c.717A= NP_005088.1:p.Ile239=
NR_131777.1:n.981A=
XM_017016911.2:c.717A= XP_016872400.1:p.Ile239=
XM_017016912.2:c.573A= XP_016872401.1:p.Ile191=
NM_005097.4:c.717A= MANE Select NP_005088.1:p.Ile239=
NM_001308275.2:c.717A= NP_001295204.1:p.Ile239=
NM_001308276.2:c.573A= NP_001295205.1:p.Ile191=
NR_131777.2:n.854A=