Canonical Allele Identifier: CA1928787553

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793203G= , CM000672.2:g.93793203G=	GRCh38
NC_000010.10:g.95552960G= , CM000672.1:g.95552960G=	GRCh37
NC_000010.9:g.95542950G=	NCBI36
NG_011832.1:g.40395G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.691G= MANE Select	ENSP00000360472.4:p.Asp231=
ENST00000485458.3:n.4667G=
ENST00000635953.1:c.691G=	ENSP00000490058.1:p.Asp231=
ENST00000636155.1:c.691G=	ENSP00000490355.1:p.Asp231=
ENST00000636232.1:c.*477G=	ENSP00000490325.1:n.*477G=
ENST00000636754.1:c.*533G=	ENSP00000489781.1:n.*533G=
ENST00000636946.1:c.*860G=	ENSP00000490654.1:n.*860G=
ENST00000637037.1:c.*281G=	ENSP00000490860.1:n.*281G=
ENST00000637347.1:n.552G=
ENST00000637611.1:c.*247G=	ENSP00000489682.1:n.*247G=
ENST00000637689.1:c.-681G=	ENSP00000490496.1:n.-681G=
ENST00000637925.1:c.*286G=	ENSP00000489763.1:n.*286G=
ENST00000638049.1:c.*449G=	ENSP00000490597.1:n.*449G=
ENST00000676175.1:n.2430G=
ENST00000371413.4:c.691G=	ENSP00000360467.3:p.Asp231=
ENST00000371418.8:c.691G=	ENSP00000360472.4:p.Asp231=
ENST00000626307.1:n.4606G=
ENST00000626946.1:n.361G=
ENST00000627420.2:c.*400G=	ENSP00000487116.1:n.*400G=
ENST00000629035.2:c.619G=	ENSP00000486908.1:p.Asp207=
ENST00000630047.2:c.547G=	ENSP00000485917.1:p.Asp183=
ENST00000630412.1:n.479G=
ENST00000630487.2:c.*481G=	ENSP00000486859.1:n.*481G=
NM_001308275.1:c.691G=	NP_001295204.1:p.Asp231=
NM_001308276.1:c.547G=	NP_001295205.1:p.Asp183=
NM_005097.2:c.691G=	NP_005088.1:p.Asp231=
NM_005097.3:c.691G=	NP_005088.1:p.Asp231=
NR_131777.1:n.955G=
XM_017016911.2:c.691G=	XP_016872400.1:p.Asp231=
XM_017016912.2:c.547G=	XP_016872401.1:p.Asp183=
NM_005097.4:c.691G= MANE Select	NP_005088.1:p.Asp231=
NM_001308275.2:c.691G=	NP_001295204.1:p.Asp231=
NM_001308276.2:c.547G=	NP_001295205.1:p.Asp183=
NR_131777.2:n.828G=