Canonical Allele Identifier: CA1928765428

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758937T= , CM000672.2:g.93758937T=	GRCh38
NC_000010.10:g.95518694T= , CM000672.1:g.95518694T=	GRCh37
NC_000010.9:g.95508684T=	NCBI36
NG_011832.1:g.6129T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+106T= MANE Select	ENSP00000360472.4:n.287+106T=
ENST00000635953.1:c.287+106T=	ENSP00000490058.1:n.287+106T=
ENST00000636140.1:n.72+106T=
ENST00000636155.1:c.287+106T=	ENSP00000490355.1:n.287+106T=
ENST00000636232.1:c.*73+106T=	ENSP00000490325.1:n.*73+106T=
ENST00000636683.1:n.42+106T=
ENST00000636754.1:c.*77+106T=	ENSP00000489781.1:n.*77+106T=
ENST00000636946.1:c.*102T=	ENSP00000490654.1:n.*102T=
ENST00000637037.1:c.287+106T=	ENSP00000490860.1:n.287+106T=
ENST00000637347.1:n.148+249T=
ENST00000637611.1:c.287+106T=	ENSP00000489682.1:n.287+106T=
ENST00000637689.1:c.-1085+106T=	ENSP00000490496.1:n.-1085+106T=
ENST00000637925.1:c.287+106T=	ENSP00000489763.1:n.287+106T=
ENST00000638049.1:c.*45+106T=	ENSP00000490597.1:n.*45+106T=
ENST00000371413.4:c.287+106T=	ENSP00000360467.3:n.287+106T=
ENST00000371418.8:c.287+106T=	ENSP00000360472.4:n.287+106T=
ENST00000627420.2:c.*77+106T=	ENSP00000487116.1:n.*77+106T=
ENST00000627699.1:c.*183T=	ENSP00000485868.1:n.*183T=
ENST00000629035.2:c.215+578T=	ENSP00000486908.1:n.215+578T=
ENST00000630047.2:c.287+106T=	ENSP00000485917.1:n.287+106T=
ENST00000630184.2:c.287+106T=	ENSP00000486607.1:n.287+106T=
ENST00000630487.2:c.*77+106T=	ENSP00000486859.1:n.*77+106T=
NM_001308275.1:c.287+106T=	NP_001295204.1:n.287+106T=
NM_001308276.1:c.287+106T=	NP_001295205.1:n.287+106T=
NM_005097.2:c.287+106T=	NP_005088.1:n.287+106T=
NM_005097.3:c.287+106T=	NP_005088.1:n.287+106T=
NR_131777.1:n.632+106T=
XM_017016911.2:c.287+106T=	XP_016872400.1:n.287+106T=
XM_017016912.2:c.287+106T=	XP_016872401.1:n.287+106T=
XR_001747552.1:n.4938A=
XR_002957095.1:n.7066A=
XR_002957096.1:n.8278A=
NM_005097.4:c.287+106T= MANE Select	NP_005088.1:n.287+106T=
NM_001308275.2:c.287+106T=	NP_001295204.1:n.287+106T=
NM_001308276.2:c.287+106T=	NP_001295205.1:n.287+106T=
NR_131777.2:n.505+106T=