Canonical Allele Identifier: CA377628296

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557093A>C (hg19) ; chr10:g.93797336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797336A>C , CM000672.2:g.93797336A>C	GRCh38
NC_000010.10:g.95557093A>C , CM000672.1:g.95557093A>C	GRCh37
NC_000010.9:g.95547083A>C	NCBI36
NG_011832.1:g.44528A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1207A>C MANE Select	ENSP00000360472.4:p.Ser403Arg
ENST00000485458.3:n.5183A>C
ENST00000635804.1:n.641A>C
ENST00000635953.1:c.*629A>C	ENSP00000490058.1:n.*629A>C
ENST00000636155.1:c.838+3986A>C	ENSP00000490355.1:n.838+3986A>C
ENST00000636232.1:c.*993A>C	ENSP00000490325.1:n.*993A>C
ENST00000636754.1:c.*1049A>C	ENSP00000489781.1:n.*1049A>C
ENST00000636946.1:c.*1008-413A>C	ENSP00000490654.1:n.*1008-413A>C
ENST00000637037.1:c.*797A>C	ENSP00000490860.1:n.*797A>C
ENST00000637347.1:n.1068A>C
ENST00000637611.1:c.*763A>C	ENSP00000489682.1:n.*763A>C
ENST00000637689.1:c.-165A>C	ENSP00000490496.1:n.-165A>C
ENST00000637925.1:c.*802A>C	ENSP00000489763.1:n.*802A>C
ENST00000638049.1:c.*965A>C	ENSP00000490597.1:n.*965A>C
ENST00000676175.1:n.2946A>C
ENST00000371413.4:c.839-413A>C	ENSP00000360467.3:n.839-413A>C
ENST00000371418.8:c.1207A>C	ENSP00000360472.4:p.Ser403Arg
ENST00000626307.1:n.5122A>C
ENST00000627420.2:c.*916A>C	ENSP00000487116.1:n.*916A>C
ENST00000629035.2:c.1135A>C	ENSP00000486908.1:p.Ser379Arg
ENST00000630047.2:c.1063A>C	ENSP00000485917.1:p.Ser355Arg
NM_001308275.1:c.839-413A>C	NP_001295204.1:n.839-413A>C
NM_001308276.1:c.1063A>C	NP_001295205.1:p.Ser355Arg
NM_005097.2:c.1207A>C	NP_005088.1:p.Ser403Arg
NM_005097.3:c.1207A>C	NP_005088.1:p.Ser403Arg
NR_131777.1:n.1471A>C
XM_017016912.2:c.695-413A>C	XP_016872401.1:n.695-413A>C
NM_005097.4:c.1207A>C MANE Select	NP_005088.1:p.Ser403Arg
NM_001308275.2:c.839-413A>C	NP_001295204.1:n.839-413A>C
NM_001308276.2:c.1063A>C	NP_001295205.1:p.Ser355Arg
NR_131777.2:n.1344A>C