Canonical Allele Identifier: CA470985270

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557018A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797261A>C , CM000672.2:g.93797261A>C	GRCh38
NC_000010.10:g.95557018A>C , CM000672.1:g.95557018A>C	GRCh37
NC_000010.9:g.95547008A>C	NCBI36
NG_011832.1:g.44453A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1132A>C MANE Select	ENSP00000360472.4:p.Arg378=
ENST00000485458.3:n.5108A>C
ENST00000635804.1:n.566A>C
ENST00000635953.1:c.*554A>C	ENSP00000490058.1:n.*554A>C
ENST00000636155.1:c.838+3911A>C	ENSP00000490355.1:n.838+3911A>C
ENST00000636232.1:c.*918A>C	ENSP00000490325.1:n.*918A>C
ENST00000636754.1:c.*974A>C	ENSP00000489781.1:n.*974A>C
ENST00000636946.1:c.*1008-488A>C	ENSP00000490654.1:n.*1008-488A>C
ENST00000637037.1:c.*722A>C	ENSP00000490860.1:n.*722A>C
ENST00000637347.1:n.993A>C
ENST00000637611.1:c.*688A>C	ENSP00000489682.1:n.*688A>C
ENST00000637689.1:c.-240A>C	ENSP00000490496.1:n.-240A>C
ENST00000637925.1:c.*727A>C	ENSP00000489763.1:n.*727A>C
ENST00000638049.1:c.*890A>C	ENSP00000490597.1:n.*890A>C
ENST00000676175.1:n.2871A>C
ENST00000371413.4:c.839-488A>C	ENSP00000360467.3:n.839-488A>C
ENST00000371418.8:c.1132A>C	ENSP00000360472.4:p.Arg378=
ENST00000626307.1:n.5047A>C
ENST00000627420.2:c.*841A>C	ENSP00000487116.1:n.*841A>C
ENST00000629035.2:c.1060A>C	ENSP00000486908.1:p.Arg354=
ENST00000630047.2:c.988A>C	ENSP00000485917.1:p.Arg330=
NM_001308275.1:c.839-488A>C	NP_001295204.1:n.839-488A>C
NM_001308276.1:c.988A>C	NP_001295205.1:p.Arg330=
NM_005097.2:c.1132A>C	NP_005088.1:p.Arg378=
NM_005097.3:c.1132A>C	NP_005088.1:p.Arg378=
NR_131777.1:n.1396A>C
XM_017016912.2:c.695-488A>C	XP_016872401.1:n.695-488A>C
NM_005097.4:c.1132A>C MANE Select	NP_005088.1:p.Arg378=
NM_001308275.2:c.839-488A>C	NP_001295204.1:n.839-488A>C
NM_001308276.2:c.988A>C	NP_001295205.1:p.Arg330=
NR_131777.2:n.1269A>C