Canonical Allele Identifier: CA2610227053
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793490C>A , CM000672.2:g.93793490C>A GRCh38
NC_000010.10:g.95553247C>A , CM000672.1:g.95553247C>A GRCh37
NC_000010.9:g.95543237C>A NCBI36
NG_011832.1:g.40682C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.838+140C>A MANE Select ENSP00000360472.4:n.838+140C>A
ENST00000485458.3:n.4814+140C>A
ENST00000635953.1:c.838+140C>A ENSP00000490058.1:n.838+140C>A
ENST00000636155.1:c.838+140C>A ENSP00000490355.1:n.838+140C>A
ENST00000636232.1:c.*624+140C>A ENSP00000490325.1:n.*624+140C>A
ENST00000636754.1:c.*680+140C>A ENSP00000489781.1:n.*680+140C>A
ENST00000636946.1:c.*1007+140C>A ENSP00000490654.1:n.*1007+140C>A
ENST00000637037.1:c.*428+140C>A ENSP00000490860.1:n.*428+140C>A
ENST00000637347.1:n.699+140C>A
ENST00000637611.1:c.*394+140C>A ENSP00000489682.1:n.*394+140C>A
ENST00000637689.1:c.-534+140C>A ENSP00000490496.1:n.-534+140C>A
ENST00000637925.1:c.*433+140C>A ENSP00000489763.1:n.*433+140C>A
ENST00000638049.1:c.*596+140C>A ENSP00000490597.1:n.*596+140C>A
ENST00000676175.1:n.2577+140C>A
ENST00000371413.4:c.838+140C>A ENSP00000360467.3:n.838+140C>A
ENST00000371418.8:c.838+140C>A ENSP00000360472.4:n.838+140C>A
ENST00000626307.1:n.4753+140C>A
ENST00000626946.1:n.508+140C>A
ENST00000627420.2:c.*547+140C>A ENSP00000487116.1:n.*547+140C>A
ENST00000629035.2:c.766+140C>A ENSP00000486908.1:n.766+140C>A
ENST00000630047.2:c.694+140C>A ENSP00000485917.1:n.694+140C>A
NM_001308275.1:c.838+140C>A NP_001295204.1:n.838+140C>A
NM_001308276.1:c.694+140C>A NP_001295205.1:n.694+140C>A
NM_005097.2:c.838+140C>A NP_005088.1:n.838+140C>A
NM_005097.3:c.838+140C>A NP_005088.1:n.838+140C>A
NR_131777.1:n.1102+140C>A
XM_017016911.2:c.838+140C>A XP_016872400.1:n.838+140C>A
XM_017016912.2:c.694+140C>A XP_016872401.1:n.694+140C>A
NM_005097.4:c.838+140C>A MANE Select NP_005088.1:n.838+140C>A
NM_001308275.2:c.838+140C>A NP_001295204.1:n.838+140C>A
NM_001308276.2:c.694+140C>A NP_001295205.1:n.694+140C>A
NR_131777.2:n.975+140C>A