Canonical Allele Identifier: CA2610220320
Gene: LGI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93758869_93758870insTTATCCAA , CM000672.2:g.93758869_93758870insTTATCCAA GRCh38
NC_000010.10:g.95518626_95518627insTTATCCAA , CM000672.1:g.95518626_95518627insTTATCCAA GRCh37
NC_000010.9:g.95508616_95508617insTTATCCAA NCBI36
NG_011832.1:g.6061_6062insTTATCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.287+38_287+39insTTATCCAA MANE Select ENSP00000360472.4:n.287+38_287+39insTTATCCAA
ENST00000635953.1:c.287+38_287+39insTTATCCAA ENSP00000490058.1:n.287+38_287+39insTTATCCAA
ENST00000636140.1:n.72+38_72+39insTTATCCAA
ENST00000636155.1:c.287+38_287+39insTTATCCAA ENSP00000490355.1:n.287+38_287+39insTTATCCAA
ENST00000636232.1:c.*73+38_*73+39insTTATCCAA ENSP00000490325.1:n.*73+38_*73+39insTTATCCAA
ENST00000636683.1:n.42+38_42+39insTTATCCAA
ENST00000636754.1:c.*77+38_*77+39insTTATCCAA ENSP00000489781.1:n.*77+38_*77+39insTTATCCAA
ENST00000636946.1:c.*34_*35insTTATCCAA ENSP00000490654.1:n.*34_*35insTTATCCAA
ENST00000637037.1:c.287+38_287+39insTTATCCAA ENSP00000490860.1:n.287+38_287+39insTTATCCAA
ENST00000637347.1:n.148+181_148+182insTTATCCAA
ENST00000637611.1:c.287+38_287+39insTTATCCAA ENSP00000489682.1:n.287+38_287+39insTTATCCAA
ENST00000637689.1:c.-1085+38_-1085+39insTTATCCAA ENSP00000490496.1:n.-1085+38_-1085+39insTTATCCAA
ENST00000637925.1:c.287+38_287+39insTTATCCAA ENSP00000489763.1:n.287+38_287+39insTTATCCAA
ENST00000638049.1:c.*45+38_*45+39insTTATCCAA ENSP00000490597.1:n.*45+38_*45+39insTTATCCAA
ENST00000371413.4:c.287+38_287+39insTTATCCAA ENSP00000360467.3:n.287+38_287+39insTTATCCAA
ENST00000371418.8:c.287+38_287+39insTTATCCAA ENSP00000360472.4:n.287+38_287+39insTTATCCAA
ENST00000478763.2:c.*34_*35insTTATCCAA ENSP00000486517.1:n.*34_*35insTTATCCAA
ENST00000627420.2:c.*77+38_*77+39insTTATCCAA ENSP00000487116.1:n.*77+38_*77+39insTTATCCAA
ENST00000627699.1:c.*115_*116insTTATCCAA ENSP00000485868.1:n.*115_*116insTTATCCAA
ENST00000629035.2:c.215+510_215+511insTTATCCAA ENSP00000486908.1:n.215+510_215+511insTTATCCAA
ENST00000630047.2:c.287+38_287+39insTTATCCAA ENSP00000485917.1:n.287+38_287+39insTTATCCAA
ENST00000630184.2:c.287+38_287+39insTTATCCAA ENSP00000486607.1:n.287+38_287+39insTTATCCAA
ENST00000630487.2:c.*77+38_*77+39insTTATCCAA ENSP00000486859.1:n.*77+38_*77+39insTTATCCAA
NM_001308275.1:c.287+38_287+39insTTATCCAA NP_001295204.1:n.287+38_287+39insTTATCCAA
NM_001308276.1:c.287+38_287+39insTTATCCAA NP_001295205.1:n.287+38_287+39insTTATCCAA
NM_005097.2:c.287+38_287+39insTTATCCAA NP_005088.1:n.287+38_287+39insTTATCCAA
NM_005097.3:c.287+38_287+39insTTATCCAA NP_005088.1:n.287+38_287+39insTTATCCAA
NR_131777.1:n.632+38_632+39insTTATCCAA
XM_017016911.2:c.287+38_287+39insTTATCCAA XP_016872400.1:n.287+38_287+39insTTATCCAA
XM_017016912.2:c.287+38_287+39insTTATCCAA XP_016872401.1:n.287+38_287+39insTTATCCAA
XR_001747552.1:n.5005_5006insTTGGATAA
XR_002957095.1:n.7133_7134insTTGGATAA
XR_002957096.1:n.8345_8346insTTGGATAA
NM_005097.4:c.287+38_287+39insTTATCCAA MANE Select NP_005088.1:n.287+38_287+39insTTATCCAA
NM_001308275.2:c.287+38_287+39insTTATCCAA NP_001295204.1:n.287+38_287+39insTTATCCAA
NM_001308276.2:c.287+38_287+39insTTATCCAA NP_001295205.1:n.287+38_287+39insTTATCCAA
NR_131777.2:n.505+38_505+39insTTATCCAA