Canonical Allele Identifier: CA1928774807

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797349G= , CM000672.2:g.93797349G=	GRCh38
NC_000010.10:g.95557106G= , CM000672.1:g.95557106G=	GRCh37
NC_000010.9:g.95547096G=	NCBI36
NG_011832.1:g.44541G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1220G= MANE Select	ENSP00000360472.4:p.Arg407=
ENST00000485458.3:n.5196G=
ENST00000635804.1:n.654G=
ENST00000635953.1:c.*642G=	ENSP00000490058.1:n.*642G=
ENST00000636155.1:c.838+3999G=	ENSP00000490355.1:n.838+3999G=
ENST00000636232.1:c.*1006G=	ENSP00000490325.1:n.*1006G=
ENST00000636754.1:c.*1062G=	ENSP00000489781.1:n.*1062G=
ENST00000636946.1:c.*1008-400G=	ENSP00000490654.1:n.*1008-400G=
ENST00000637037.1:c.*810G=	ENSP00000490860.1:n.*810G=
ENST00000637347.1:n.1081G=
ENST00000637611.1:c.*776G=	ENSP00000489682.1:n.*776G=
ENST00000637689.1:c.-152G=	ENSP00000490496.1:n.-152G=
ENST00000637925.1:c.*815G=	ENSP00000489763.1:n.*815G=
ENST00000638049.1:c.*978G=	ENSP00000490597.1:n.*978G=
ENST00000676175.1:n.2959G=
ENST00000371413.4:c.839-400G=	ENSP00000360467.3:n.839-400G=
ENST00000371418.8:c.1220G=	ENSP00000360472.4:p.Arg407=
ENST00000626307.1:n.5135G=
ENST00000627420.2:c.*929G=	ENSP00000487116.1:n.*929G=
ENST00000629035.2:c.1148G=	ENSP00000486908.1:p.Arg383=
ENST00000630047.2:c.1076G=	ENSP00000485917.1:p.Arg359=
NM_001308275.1:c.839-400G=	NP_001295204.1:n.839-400G=
NM_001308276.1:c.1076G=	NP_001295205.1:p.Arg359=
NM_005097.2:c.1220G=	NP_005088.1:p.Arg407=
NM_005097.3:c.1220G=	NP_005088.1:p.Arg407=
NR_131777.1:n.1484G=
XM_017016912.2:c.695-400G=	XP_016872401.1:n.695-400G=
NM_005097.4:c.1220G= MANE Select	NP_005088.1:p.Arg407=
NM_001308275.2:c.839-400G=	NP_001295204.1:n.839-400G=
NM_001308276.2:c.1076G=	NP_001295205.1:p.Arg359=
NR_131777.2:n.1357G=