Canonical Allele Identifier: CA1928787560
Gene: LGI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93793206C= , CM000672.2:g.93793206C= GRCh38
NC_000010.10:g.95552963C= , CM000672.1:g.95552963C= GRCh37
NC_000010.9:g.95542953C= NCBI36
NG_011832.1:g.40398C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371418.9:c.694C= MANE Select ENSP00000360472.4:p.Leu232=
ENST00000485458.3:n.4670C=
ENST00000635953.1:c.694C= ENSP00000490058.1:p.Leu232=
ENST00000636155.1:c.694C= ENSP00000490355.1:p.Leu232=
ENST00000636232.1:c.*480C= ENSP00000490325.1:n.*480C=
ENST00000636754.1:c.*536C= ENSP00000489781.1:n.*536C=
ENST00000636946.1:c.*863C= ENSP00000490654.1:n.*863C=
ENST00000637037.1:c.*284C= ENSP00000490860.1:n.*284C=
ENST00000637347.1:n.555C=
ENST00000637611.1:c.*250C= ENSP00000489682.1:n.*250C=
ENST00000637689.1:c.-678C= ENSP00000490496.1:n.-678C=
ENST00000637925.1:c.*289C= ENSP00000489763.1:n.*289C=
ENST00000638049.1:c.*452C= ENSP00000490597.1:n.*452C=
ENST00000676175.1:n.2433C=
ENST00000371413.4:c.694C= ENSP00000360467.3:p.Leu232=
ENST00000371418.8:c.694C= ENSP00000360472.4:p.Leu232=
ENST00000626307.1:n.4609C=
ENST00000626946.1:n.364C=
ENST00000627420.2:c.*403C= ENSP00000487116.1:n.*403C=
ENST00000629035.2:c.622C= ENSP00000486908.1:p.Leu208=
ENST00000630047.2:c.550C= ENSP00000485917.1:p.Leu184=
ENST00000630412.1:n.482C=
ENST00000630487.2:c.*484C= ENSP00000486859.1:n.*484C=
NM_001308275.1:c.694C= NP_001295204.1:p.Leu232=
NM_001308276.1:c.550C= NP_001295205.1:p.Leu184=
NM_005097.2:c.694C= NP_005088.1:p.Leu232=
NM_005097.3:c.694C= NP_005088.1:p.Leu232=
NR_131777.1:n.958C=
XM_017016911.2:c.694C= XP_016872400.1:p.Leu232=
XM_017016912.2:c.550C= XP_016872401.1:p.Leu184=
NM_005097.4:c.694C= MANE Select NP_005088.1:p.Leu232=
NM_001308275.2:c.694C= NP_001295204.1:p.Leu232=
NM_001308276.2:c.550C= NP_001295205.1:p.Leu184=
NR_131777.2:n.831C=