Canonical Allele Identifier: CA1928771009
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793347A= , CM000672.2:g.93793347A= GRCh38
NC_000010.10:g.95553104A= , CM000672.1:g.95553104A= GRCh37
NC_000010.9:g.95543094A= NCBI36
NG_011832.1:g.40539A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.835A= MANE Select ENSP00000360472.4:p.Thr279=
ENST00000485458.3:n.4811A=
ENST00000635953.1:c.835A= ENSP00000490058.1:p.Thr279=
ENST00000636155.1:c.835A= ENSP00000490355.1:p.Thr279=
ENST00000636232.1:c.*621A= ENSP00000490325.1:n.*621A=
ENST00000636754.1:c.*677A= ENSP00000489781.1:n.*677A=
ENST00000636946.1:c.*1004A= ENSP00000490654.1:n.*1004A=
ENST00000637037.1:c.*425A= ENSP00000490860.1:n.*425A=
ENST00000637347.1:n.696A=
ENST00000637611.1:c.*391A= ENSP00000489682.1:n.*391A=
ENST00000637689.1:c.-537A= ENSP00000490496.1:n.-537A=
ENST00000637925.1:c.*430A= ENSP00000489763.1:n.*430A=
ENST00000638049.1:c.*593A= ENSP00000490597.1:n.*593A=
ENST00000676175.1:n.2574A=
ENST00000371413.4:c.835A= ENSP00000360467.3:p.Thr279=
ENST00000371418.8:c.835A= ENSP00000360472.4:p.Thr279=
ENST00000626307.1:n.4750A=
ENST00000626946.1:n.505A=
ENST00000627420.2:c.*544A= ENSP00000487116.1:n.*544A=
ENST00000629035.2:c.763A= ENSP00000486908.1:p.Thr255=
ENST00000630047.2:c.691A= ENSP00000485917.1:p.Thr231=
ENST00000630487.2:c.*625A= ENSP00000486859.1:n.*625A=
NM_001308275.1:c.835A= NP_001295204.1:p.Thr279=
NM_001308276.1:c.691A= NP_001295205.1:p.Thr231=
NM_005097.2:c.835A= NP_005088.1:p.Thr279=
NM_005097.3:c.835A= NP_005088.1:p.Thr279=
NR_131777.1:n.1099A=
XM_017016911.2:c.835A= XP_016872400.1:p.Thr279=
XM_017016912.2:c.691A= XP_016872401.1:p.Thr231=
NM_005097.4:c.835A= MANE Select NP_005088.1:p.Thr279=
NM_001308275.2:c.835A= NP_001295204.1:p.Thr279=
NM_001308276.2:c.691A= NP_001295205.1:p.Thr231=
NR_131777.2:n.972A=