Canonical Allele Identifier: CA1928770974

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793328C= , CM000672.2:g.93793328C=	GRCh38
NC_000010.10:g.95553085C= , CM000672.1:g.95553085C=	GRCh37
NC_000010.9:g.95543075C=	NCBI36
NG_011832.1:g.40520C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.816C= MANE Select	ENSP00000360472.4:p.Phe272=
ENST00000485458.3:n.4792C=
ENST00000635953.1:c.816C=	ENSP00000490058.1:p.Phe272=
ENST00000636155.1:c.816C=	ENSP00000490355.1:p.Phe272=
ENST00000636232.1:c.*602C=	ENSP00000490325.1:n.*602C=
ENST00000636754.1:c.*658C=	ENSP00000489781.1:n.*658C=
ENST00000636946.1:c.*985C=	ENSP00000490654.1:n.*985C=
ENST00000637037.1:c.*406C=	ENSP00000490860.1:n.*406C=
ENST00000637347.1:n.677C=
ENST00000637611.1:c.*372C=	ENSP00000489682.1:n.*372C=
ENST00000637689.1:c.-556C=	ENSP00000490496.1:n.-556C=
ENST00000637925.1:c.*411C=	ENSP00000489763.1:n.*411C=
ENST00000638049.1:c.*574C=	ENSP00000490597.1:n.*574C=
ENST00000676175.1:n.2555C=
ENST00000371413.4:c.816C=	ENSP00000360467.3:p.Phe272=
ENST00000371418.8:c.816C=	ENSP00000360472.4:p.Phe272=
ENST00000626307.1:n.4731C=
ENST00000626946.1:n.486C=
ENST00000627420.2:c.*525C=	ENSP00000487116.1:n.*525C=
ENST00000629035.2:c.744C=	ENSP00000486908.1:p.Phe248=
ENST00000630047.2:c.672C=	ENSP00000485917.1:p.Phe224=
ENST00000630487.2:c.*606C=	ENSP00000486859.1:n.*606C=
NM_001308275.1:c.816C=	NP_001295204.1:p.Phe272=
NM_001308276.1:c.672C=	NP_001295205.1:p.Phe224=
NM_005097.2:c.816C=	NP_005088.1:p.Phe272=
NM_005097.3:c.816C=	NP_005088.1:p.Phe272=
NR_131777.1:n.1080C=
XM_017016911.2:c.816C=	XP_016872400.1:p.Phe272=
XM_017016912.2:c.672C=	XP_016872401.1:p.Phe224=
NM_005097.4:c.816C= MANE Select	NP_005088.1:p.Phe272=
NM_001308275.2:c.816C=	NP_001295204.1:p.Phe272=
NM_001308276.2:c.672C=	NP_001295205.1:p.Phe224=
NR_131777.2:n.953C=