Canonical Allele Identifier: CA377623992
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793215C>G , CM000672.2:g.93793215C>G GRCh38
NC_000010.10:g.95552972C>G , CM000672.1:g.95552972C>G GRCh37
NC_000010.9:g.95542962C>G NCBI36
NG_011832.1:g.40407C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.703C>G MANE Select ENSP00000360472.4:p.Gln235Glu
ENST00000485458.3:n.4679C>G
ENST00000635953.1:c.703C>G ENSP00000490058.1:p.Gln235Glu
ENST00000636155.1:c.703C>G ENSP00000490355.1:p.Gln235Glu
ENST00000636232.1:c.*489C>G ENSP00000490325.1:n.*489C>G
ENST00000636754.1:c.*545C>G ENSP00000489781.1:n.*545C>G
ENST00000636946.1:c.*872C>G ENSP00000490654.1:n.*872C>G
ENST00000637037.1:c.*293C>G ENSP00000490860.1:n.*293C>G
ENST00000637347.1:n.564C>G
ENST00000637611.1:c.*259C>G ENSP00000489682.1:n.*259C>G
ENST00000637689.1:c.-669C>G ENSP00000490496.1:n.-669C>G
ENST00000637925.1:c.*298C>G ENSP00000489763.1:n.*298C>G
ENST00000638049.1:c.*461C>G ENSP00000490597.1:n.*461C>G
ENST00000676175.1:n.2442C>G
ENST00000371413.4:c.703C>G ENSP00000360467.3:p.Gln235Glu
ENST00000371418.8:c.703C>G ENSP00000360472.4:p.Gln235Glu
ENST00000626307.1:n.4618C>G
ENST00000626946.1:n.373C>G
ENST00000627420.2:c.*412C>G ENSP00000487116.1:n.*412C>G
ENST00000629035.2:c.631C>G ENSP00000486908.1:p.Gln211Glu
ENST00000630047.2:c.559C>G ENSP00000485917.1:p.Gln187Glu
ENST00000630412.1:n.491C>G
ENST00000630487.2:c.*493C>G ENSP00000486859.1:n.*493C>G
NM_001308275.1:c.703C>G NP_001295204.1:p.Gln235Glu
NM_001308276.1:c.559C>G NP_001295205.1:p.Gln187Glu
NM_005097.2:c.703C>G NP_005088.1:p.Gln235Glu
NM_005097.3:c.703C>G NP_005088.1:p.Gln235Glu
NR_131777.1:n.967C>G
XM_017016911.2:c.703C>G XP_016872400.1:p.Gln235Glu
XM_017016912.2:c.559C>G XP_016872401.1:p.Gln187Glu
NM_005097.4:c.703C>G MANE Select NP_005088.1:p.Gln235Glu
NM_001308275.2:c.703C>G NP_001295204.1:p.Gln235Glu
NM_001308276.2:c.559C>G NP_001295205.1:p.Gln187Glu
NR_131777.2:n.840C>G