Canonical Allele Identifier: CA1928787578

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793217A= , CM000672.2:g.93793217A=	GRCh38
NC_000010.10:g.95552974A= , CM000672.1:g.95552974A=	GRCh37
NC_000010.9:g.95542964A=	NCBI36
NG_011832.1:g.40409A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.705A= MANE Select	ENSP00000360472.4:p.Gln235=
ENST00000485458.3:n.4681A=
ENST00000635953.1:c.705A=	ENSP00000490058.1:p.Gln235=
ENST00000636155.1:c.705A=	ENSP00000490355.1:p.Gln235=
ENST00000636232.1:c.*491A=	ENSP00000490325.1:n.*491A=
ENST00000636754.1:c.*547A=	ENSP00000489781.1:n.*547A=
ENST00000636946.1:c.*874A=	ENSP00000490654.1:n.*874A=
ENST00000637037.1:c.*295A=	ENSP00000490860.1:n.*295A=
ENST00000637347.1:n.566A=
ENST00000637611.1:c.*261A=	ENSP00000489682.1:n.*261A=
ENST00000637689.1:c.-667A=	ENSP00000490496.1:n.-667A=
ENST00000637925.1:c.*300A=	ENSP00000489763.1:n.*300A=
ENST00000638049.1:c.*463A=	ENSP00000490597.1:n.*463A=
ENST00000676175.1:n.2444A=
ENST00000371413.4:c.705A=	ENSP00000360467.3:p.Gln235=
ENST00000371418.8:c.705A=	ENSP00000360472.4:p.Gln235=
ENST00000626307.1:n.4620A=
ENST00000626946.1:n.375A=
ENST00000627420.2:c.*414A=	ENSP00000487116.1:n.*414A=
ENST00000629035.2:c.633A=	ENSP00000486908.1:p.Gln211=
ENST00000630047.2:c.561A=	ENSP00000485917.1:p.Gln187=
ENST00000630412.1:n.493A=
ENST00000630487.2:c.*495A=	ENSP00000486859.1:n.*495A=
NM_001308275.1:c.705A=	NP_001295204.1:p.Gln235=
NM_001308276.1:c.561A=	NP_001295205.1:p.Gln187=
NM_005097.2:c.705A=	NP_005088.1:p.Gln235=
NM_005097.3:c.705A=	NP_005088.1:p.Gln235=
NR_131777.1:n.969A=
XM_017016911.2:c.705A=	XP_016872400.1:p.Gln235=
XM_017016912.2:c.561A=	XP_016872401.1:p.Gln187=
NM_005097.4:c.705A= MANE Select	NP_005088.1:p.Gln235=
NM_001308275.2:c.705A=	NP_001295204.1:p.Gln235=
NM_001308276.2:c.561A=	NP_001295205.1:p.Gln187=
NR_131777.2:n.842A=