Canonical Allele Identifier: CA1928787429

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793008C= , CM000672.2:g.93793008C=	GRCh38
NC_000010.10:g.95552765C= , CM000672.1:g.95552765C=	GRCh37
NC_000010.9:g.95542755C=	NCBI36
NG_011832.1:g.40200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.673+96C= MANE Select	ENSP00000360472.4:n.673+96C=
ENST00000485458.3:n.4649+96C=
ENST00000635953.1:c.673+96C=	ENSP00000490058.1:n.673+96C=
ENST00000636155.1:c.673+96C=	ENSP00000490355.1:n.673+96C=
ENST00000636232.1:c.*459+96C=	ENSP00000490325.1:n.*459+96C=
ENST00000636754.1:c.*515+96C=	ENSP00000489781.1:n.*515+96C=
ENST00000636946.1:c.*842+96C=	ENSP00000490654.1:n.*842+96C=
ENST00000637037.1:c.*263+96C=	ENSP00000490860.1:n.*263+96C=
ENST00000637347.1:n.534+96C=
ENST00000637611.1:c.*229+96C=	ENSP00000489682.1:n.*229+96C=
ENST00000637689.1:c.-699+96C=	ENSP00000490496.1:n.-699+96C=
ENST00000637925.1:c.*268+96C=	ENSP00000489763.1:n.*268+96C=
ENST00000638049.1:c.*431+96C=	ENSP00000490597.1:n.*431+96C=
ENST00000676175.1:n.2412+96C=
ENST00000371413.4:c.673+96C=	ENSP00000360467.3:n.673+96C=
ENST00000371418.8:c.673+96C=	ENSP00000360472.4:n.673+96C=
ENST00000626307.1:n.4588+96C=
ENST00000626946.1:n.166C=
ENST00000627420.2:c.*382+96C=	ENSP00000487116.1:n.*382+96C=
ENST00000629035.2:c.601+96C=	ENSP00000486908.1:n.601+96C=
ENST00000630047.2:c.529+96C=	ENSP00000485917.1:n.529+96C=
ENST00000630412.1:n.461+96C=
ENST00000630487.2:c.*463+96C=	ENSP00000486859.1:n.*463+96C=
NM_001308275.1:c.673+96C=	NP_001295204.1:n.673+96C=
NM_001308276.1:c.529+96C=	NP_001295205.1:n.529+96C=
NM_005097.2:c.673+96C=	NP_005088.1:n.673+96C=
NM_005097.3:c.673+96C=	NP_005088.1:n.673+96C=
NR_131777.1:n.937+96C=
XM_017016911.2:c.673+96C=	XP_016872400.1:n.673+96C=
XM_017016912.2:c.529+96C=	XP_016872401.1:n.529+96C=
NM_005097.4:c.673+96C= MANE Select	NP_005088.1:n.673+96C=
NM_001308275.2:c.673+96C=	NP_001295204.1:n.673+96C=
NM_001308276.2:c.529+96C=	NP_001295205.1:n.529+96C=
NR_131777.2:n.810+96C=