Canonical Allele Identifier: CA2610226497
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793051_93793054dup , CM000672.2:g.93793051_93793054dup GRCh38
NC_000010.10:g.95552808_95552811dup , CM000672.1:g.95552808_95552811dup GRCh37
NC_000010.9:g.95542798_95542801dup NCBI36
NG_011832.1:g.40243_40246dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.674-135_674-132dup MANE Select ENSP00000360472.4:n.674-135_674-132dup
ENST00000485458.3:n.4650-135_4650-132dup
ENST00000635953.1:c.674-135_674-132dup ENSP00000490058.1:n.674-135_674-132dup
ENST00000636155.1:c.674-135_674-132dup ENSP00000490355.1:n.674-135_674-132dup
ENST00000636232.1:c.*460-135_*460-132dup ENSP00000490325.1:n.*460-135_*460-132dup
ENST00000636754.1:c.*516-135_*516-132dup ENSP00000489781.1:n.*516-135_*516-132dup
ENST00000636946.1:c.*843-135_*843-132dup ENSP00000490654.1:n.*843-135_*843-132dup
ENST00000637037.1:c.*264-135_*264-132dup ENSP00000490860.1:n.*264-135_*264-132dup
ENST00000637347.1:n.535-135_535-132dup
ENST00000637611.1:c.*230-135_*230-132dup ENSP00000489682.1:n.*230-135_*230-132dup
ENST00000637689.1:c.-698-135_-698-132dup ENSP00000490496.1:n.-698-135_-698-132dup
ENST00000637925.1:c.*269-135_*269-132dup ENSP00000489763.1:n.*269-135_*269-132dup
ENST00000638049.1:c.*432-135_*432-132dup ENSP00000490597.1:n.*432-135_*432-132dup
ENST00000676175.1:n.2413-135_2413-132dup
ENST00000371413.4:c.674-135_674-132dup ENSP00000360467.3:n.674-135_674-132dup
ENST00000371418.8:c.674-135_674-132dup ENSP00000360472.4:n.674-135_674-132dup
ENST00000626307.1:n.4589-135_4589-132dup
ENST00000626946.1:n.209_212dup
ENST00000627420.2:c.*383-135_*383-132dup ENSP00000487116.1:n.*383-135_*383-132dup
ENST00000629035.2:c.602-135_602-132dup ENSP00000486908.1:n.602-135_602-132dup
ENST00000630047.2:c.530-135_530-132dup ENSP00000485917.1:n.530-135_530-132dup
ENST00000630412.1:n.462-135_462-132dup
ENST00000630487.2:c.*464-135_*464-132dup ENSP00000486859.1:n.*464-135_*464-132dup
NM_001308275.1:c.674-135_674-132dup NP_001295204.1:n.674-135_674-132dup
NM_001308276.1:c.530-135_530-132dup NP_001295205.1:n.530-135_530-132dup
NM_005097.2:c.674-135_674-132dup NP_005088.1:n.674-135_674-132dup
NM_005097.3:c.674-135_674-132dup NP_005088.1:n.674-135_674-132dup
NR_131777.1:n.938-135_938-132dup
XM_017016911.2:c.674-135_674-132dup XP_016872400.1:n.674-135_674-132dup
XM_017016912.2:c.530-135_530-132dup XP_016872401.1:n.530-135_530-132dup
NM_005097.4:c.674-135_674-132dup MANE Select NP_005088.1:n.674-135_674-132dup
NM_001308275.2:c.674-135_674-132dup NP_001295204.1:n.674-135_674-132dup
NM_001308276.2:c.530-135_530-132dup NP_001295205.1:n.530-135_530-132dup
NR_131777.2:n.811-135_811-132dup