Canonical Allele Identifier: CA2610226539
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793086T>C , CM000672.2:g.93793086T>C GRCh38
NC_000010.10:g.95552843T>C , CM000672.1:g.95552843T>C GRCh37
NC_000010.9:g.95542833T>C NCBI36
NG_011832.1:g.40278T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.674-100T>C MANE Select ENSP00000360472.4:n.674-100T>C
ENST00000485458.3:n.4650-100T>C
ENST00000635953.1:c.674-100T>C ENSP00000490058.1:n.674-100T>C
ENST00000636155.1:c.674-100T>C ENSP00000490355.1:n.674-100T>C
ENST00000636232.1:c.*460-100T>C ENSP00000490325.1:n.*460-100T>C
ENST00000636754.1:c.*516-100T>C ENSP00000489781.1:n.*516-100T>C
ENST00000636946.1:c.*843-100T>C ENSP00000490654.1:n.*843-100T>C
ENST00000637037.1:c.*264-100T>C ENSP00000490860.1:n.*264-100T>C
ENST00000637347.1:n.535-100T>C
ENST00000637611.1:c.*230-100T>C ENSP00000489682.1:n.*230-100T>C
ENST00000637689.1:c.-698-100T>C ENSP00000490496.1:n.-698-100T>C
ENST00000637925.1:c.*269-100T>C ENSP00000489763.1:n.*269-100T>C
ENST00000638049.1:c.*432-100T>C ENSP00000490597.1:n.*432-100T>C
ENST00000676175.1:n.2413-100T>C
ENST00000371413.4:c.674-100T>C ENSP00000360467.3:n.674-100T>C
ENST00000371418.8:c.674-100T>C ENSP00000360472.4:n.674-100T>C
ENST00000626307.1:n.4589-100T>C
ENST00000626946.1:n.244T>C
ENST00000627420.2:c.*383-100T>C ENSP00000487116.1:n.*383-100T>C
ENST00000629035.2:c.602-100T>C ENSP00000486908.1:n.602-100T>C
ENST00000630047.2:c.530-100T>C ENSP00000485917.1:n.530-100T>C
ENST00000630412.1:n.462-100T>C
ENST00000630487.2:c.*464-100T>C ENSP00000486859.1:n.*464-100T>C
NM_001308275.1:c.674-100T>C NP_001295204.1:n.674-100T>C
NM_001308276.1:c.530-100T>C NP_001295205.1:n.530-100T>C
NM_005097.2:c.674-100T>C NP_005088.1:n.674-100T>C
NM_005097.3:c.674-100T>C NP_005088.1:n.674-100T>C
NR_131777.1:n.938-100T>C
XM_017016911.2:c.674-100T>C XP_016872400.1:n.674-100T>C
XM_017016912.2:c.530-100T>C XP_016872401.1:n.530-100T>C
NM_005097.4:c.674-100T>C MANE Select NP_005088.1:n.674-100T>C
NM_001308275.2:c.674-100T>C NP_001295204.1:n.674-100T>C
NM_001308276.2:c.530-100T>C NP_001295205.1:n.530-100T>C
NR_131777.2:n.811-100T>C