Canonical Allele Identifier: CA1928771046

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793369T= , CM000672.2:g.93793369T=	GRCh38
NC_000010.10:g.95553126T= , CM000672.1:g.95553126T=	GRCh37
NC_000010.9:g.95543116T=	NCBI36
NG_011832.1:g.40561T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838+19T= MANE Select	ENSP00000360472.4:n.838+19T=
ENST00000485458.3:n.4814+19T=
ENST00000635953.1:c.838+19T=	ENSP00000490058.1:n.838+19T=
ENST00000636155.1:c.838+19T=	ENSP00000490355.1:n.838+19T=
ENST00000636232.1:c.*624+19T=	ENSP00000490325.1:n.*624+19T=
ENST00000636754.1:c.*680+19T=	ENSP00000489781.1:n.*680+19T=
ENST00000636946.1:c.*1007+19T=	ENSP00000490654.1:n.*1007+19T=
ENST00000637037.1:c.*428+19T=	ENSP00000490860.1:n.*428+19T=
ENST00000637347.1:n.699+19T=
ENST00000637611.1:c.*394+19T=	ENSP00000489682.1:n.*394+19T=
ENST00000637689.1:c.-534+19T=	ENSP00000490496.1:n.-534+19T=
ENST00000637925.1:c.*433+19T=	ENSP00000489763.1:n.*433+19T=
ENST00000638049.1:c.*596+19T=	ENSP00000490597.1:n.*596+19T=
ENST00000676175.1:n.2577+19T=
ENST00000371413.4:c.838+19T=	ENSP00000360467.3:n.838+19T=
ENST00000371418.8:c.838+19T=	ENSP00000360472.4:n.838+19T=
ENST00000626307.1:n.4753+19T=
ENST00000626946.1:n.508+19T=
ENST00000627420.2:c.*547+19T=	ENSP00000487116.1:n.*547+19T=
ENST00000629035.2:c.766+19T=	ENSP00000486908.1:n.766+19T=
ENST00000630047.2:c.694+19T=	ENSP00000485917.1:n.694+19T=
NM_001308275.1:c.838+19T=	NP_001295204.1:n.838+19T=
NM_001308276.1:c.694+19T=	NP_001295205.1:n.694+19T=
NM_005097.2:c.838+19T=	NP_005088.1:n.838+19T=
NM_005097.3:c.838+19T=	NP_005088.1:n.838+19T=
NR_131777.1:n.1102+19T=
XM_017016911.2:c.838+19T=	XP_016872400.1:n.838+19T=
XM_017016912.2:c.694+19T=	XP_016872401.1:n.694+19T=
NM_005097.4:c.838+19T= MANE Select	NP_005088.1:n.838+19T=
NM_001308275.2:c.838+19T=	NP_001295204.1:n.838+19T=
NM_001308276.2:c.694+19T=	NP_001295205.1:n.694+19T=
NR_131777.2:n.975+19T=