Canonical Allele Identifier: CA1928765415
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93758907T= , CM000672.2:g.93758907T= GRCh38
NC_000010.10:g.95518664T= , CM000672.1:g.95518664T= GRCh37
NC_000010.9:g.95508654T= NCBI36
NG_011832.1:g.6099T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.287+76T= MANE Select ENSP00000360472.4:n.287+76T=
ENST00000635953.1:c.287+76T= ENSP00000490058.1:n.287+76T=
ENST00000636140.1:n.72+76T=
ENST00000636155.1:c.287+76T= ENSP00000490355.1:n.287+76T=
ENST00000636232.1:c.*73+76T= ENSP00000490325.1:n.*73+76T=
ENST00000636683.1:n.42+76T=
ENST00000636754.1:c.*77+76T= ENSP00000489781.1:n.*77+76T=
ENST00000636946.1:c.*72T= ENSP00000490654.1:n.*72T=
ENST00000637037.1:c.287+76T= ENSP00000490860.1:n.287+76T=
ENST00000637347.1:n.148+219T=
ENST00000637611.1:c.287+76T= ENSP00000489682.1:n.287+76T=
ENST00000637689.1:c.-1085+76T= ENSP00000490496.1:n.-1085+76T=
ENST00000637925.1:c.287+76T= ENSP00000489763.1:n.287+76T=
ENST00000638049.1:c.*45+76T= ENSP00000490597.1:n.*45+76T=
ENST00000371413.4:c.287+76T= ENSP00000360467.3:n.287+76T=
ENST00000371418.8:c.287+76T= ENSP00000360472.4:n.287+76T=
ENST00000478763.2:c.*72T= ENSP00000486517.1:n.*72T=
ENST00000627420.2:c.*77+76T= ENSP00000487116.1:n.*77+76T=
ENST00000627699.1:c.*153T= ENSP00000485868.1:n.*153T=
ENST00000629035.2:c.215+548T= ENSP00000486908.1:n.215+548T=
ENST00000630047.2:c.287+76T= ENSP00000485917.1:n.287+76T=
ENST00000630184.2:c.287+76T= ENSP00000486607.1:n.287+76T=
ENST00000630487.2:c.*77+76T= ENSP00000486859.1:n.*77+76T=
NM_001308275.1:c.287+76T= NP_001295204.1:n.287+76T=
NM_001308276.1:c.287+76T= NP_001295205.1:n.287+76T=
NM_005097.2:c.287+76T= NP_005088.1:n.287+76T=
NM_005097.3:c.287+76T= NP_005088.1:n.287+76T=
NR_131777.1:n.632+76T=
XM_017016911.2:c.287+76T= XP_016872400.1:n.287+76T=
XM_017016912.2:c.287+76T= XP_016872401.1:n.287+76T=
XR_001747552.1:n.4968A=
XR_002957095.1:n.7096A=
XR_002957096.1:n.8308A=
NM_005097.4:c.287+76T= MANE Select NP_005088.1:n.287+76T=
NM_001308275.2:c.287+76T= NP_001295204.1:n.287+76T=
NM_001308276.2:c.287+76T= NP_001295205.1:n.287+76T=
NR_131777.2:n.505+76T=