Canonical Allele Identifier: CA1928787532

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793192C= , CM000672.2:g.93793192C=	GRCh38
NC_000010.10:g.95552949C= , CM000672.1:g.95552949C=	GRCh37
NC_000010.9:g.95542939C=	NCBI36
NG_011832.1:g.40384C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.680C= MANE Select	ENSP00000360472.4:p.Ala227=
ENST00000485458.3:n.4656C=
ENST00000635953.1:c.680C=	ENSP00000490058.1:p.Ala227=
ENST00000636155.1:c.680C=	ENSP00000490355.1:p.Ala227=
ENST00000636232.1:c.*466C=	ENSP00000490325.1:n.*466C=
ENST00000636754.1:c.*522C=	ENSP00000489781.1:n.*522C=
ENST00000636946.1:c.*849C=	ENSP00000490654.1:n.*849C=
ENST00000637037.1:c.*270C=	ENSP00000490860.1:n.*270C=
ENST00000637347.1:n.541C=
ENST00000637611.1:c.*236C=	ENSP00000489682.1:n.*236C=
ENST00000637689.1:c.-692C=	ENSP00000490496.1:n.-692C=
ENST00000637925.1:c.*275C=	ENSP00000489763.1:n.*275C=
ENST00000638049.1:c.*438C=	ENSP00000490597.1:n.*438C=
ENST00000676175.1:n.2419C=
ENST00000371413.4:c.680C=	ENSP00000360467.3:p.Ala227=
ENST00000371418.8:c.680C=	ENSP00000360472.4:p.Ala227=
ENST00000626307.1:n.4595C=
ENST00000626946.1:n.350C=
ENST00000627420.2:c.*389C=	ENSP00000487116.1:n.*389C=
ENST00000629035.2:c.608C=	ENSP00000486908.1:p.Ala203=
ENST00000630047.2:c.536C=	ENSP00000485917.1:p.Ala179=
ENST00000630412.1:n.468C=
ENST00000630487.2:c.*470C=	ENSP00000486859.1:n.*470C=
NM_001308275.1:c.680C=	NP_001295204.1:p.Ala227=
NM_001308276.1:c.536C=	NP_001295205.1:p.Ala179=
NM_005097.2:c.680C=	NP_005088.1:p.Ala227=
NM_005097.3:c.680C=	NP_005088.1:p.Ala227=
NR_131777.1:n.944C=
XM_017016911.2:c.680C=	XP_016872400.1:p.Ala227=
XM_017016912.2:c.536C=	XP_016872401.1:p.Ala179=
NM_005097.4:c.680C= MANE Select	NP_005088.1:p.Ala227=
NM_001308275.2:c.680C=	NP_001295204.1:p.Ala227=
NM_001308276.2:c.536C=	NP_001295205.1:p.Ala179=
NR_131777.2:n.817C=