Canonical Allele Identifier: CA2610226511
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793061_93793066del , CM000672.2:g.93793061_93793066del GRCh38
NC_000010.10:g.95552818_95552823del , CM000672.1:g.95552818_95552823del GRCh37
NC_000010.9:g.95542808_95542813del NCBI36
NG_011832.1:g.40253_40258del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.674-125_674-120del MANE Select ENSP00000360472.4:n.674-125_674-120del
ENST00000485458.3:n.4650-125_4650-120del
ENST00000635953.1:c.674-125_674-120del ENSP00000490058.1:n.674-125_674-120del
ENST00000636155.1:c.674-125_674-120del ENSP00000490355.1:n.674-125_674-120del
ENST00000636232.1:c.*460-125_*460-120del ENSP00000490325.1:n.*460-125_*460-120del
ENST00000636754.1:c.*516-125_*516-120del ENSP00000489781.1:n.*516-125_*516-120del
ENST00000636946.1:c.*843-125_*843-120del ENSP00000490654.1:n.*843-125_*843-120del
ENST00000637037.1:c.*264-125_*264-120del ENSP00000490860.1:n.*264-125_*264-120del
ENST00000637347.1:n.535-125_535-120del
ENST00000637611.1:c.*230-125_*230-120del ENSP00000489682.1:n.*230-125_*230-120del
ENST00000637689.1:c.-698-125_-698-120del ENSP00000490496.1:n.-698-125_-698-120del
ENST00000637925.1:c.*269-125_*269-120del ENSP00000489763.1:n.*269-125_*269-120del
ENST00000638049.1:c.*432-125_*432-120del ENSP00000490597.1:n.*432-125_*432-120del
ENST00000676175.1:n.2413-125_2413-120del
ENST00000371413.4:c.674-125_674-120del ENSP00000360467.3:n.674-125_674-120del
ENST00000371418.8:c.674-125_674-120del ENSP00000360472.4:n.674-125_674-120del
ENST00000626307.1:n.4589-125_4589-120del
ENST00000626946.1:n.219_224del
ENST00000627420.2:c.*383-125_*383-120del ENSP00000487116.1:n.*383-125_*383-120del
ENST00000629035.2:c.602-125_602-120del ENSP00000486908.1:n.602-125_602-120del
ENST00000630047.2:c.530-125_530-120del ENSP00000485917.1:n.530-125_530-120del
ENST00000630412.1:n.462-125_462-120del
ENST00000630487.2:c.*464-125_*464-120del ENSP00000486859.1:n.*464-125_*464-120del
NM_001308275.1:c.674-125_674-120del NP_001295204.1:n.674-125_674-120del
NM_001308276.1:c.530-125_530-120del NP_001295205.1:n.530-125_530-120del
NM_005097.2:c.674-125_674-120del NP_005088.1:n.674-125_674-120del
NM_005097.3:c.674-125_674-120del NP_005088.1:n.674-125_674-120del
NR_131777.1:n.938-125_938-120del
XM_017016911.2:c.674-125_674-120del XP_016872400.1:n.674-125_674-120del
XM_017016912.2:c.530-125_530-120del XP_016872401.1:n.530-125_530-120del
NM_005097.4:c.674-125_674-120del MANE Select NP_005088.1:n.674-125_674-120del
NM_001308275.2:c.674-125_674-120del NP_001295204.1:n.674-125_674-120del
NM_001308276.2:c.530-125_530-120del NP_001295205.1:n.530-125_530-120del
NR_131777.2:n.811-125_811-120del