Canonical Allele Identifier: CA377627179

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556917G>C (hg19) ; chr10:g.93797160G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797160G>C , CM000672.2:g.93797160G>C	GRCh38
NC_000010.10:g.95556917G>C , CM000672.1:g.95556917G>C	GRCh37
NC_000010.9:g.95546907G>C	NCBI36
NG_011832.1:g.44352G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1031G>C MANE Select	ENSP00000360472.4:p.Trp344Ser
ENST00000485458.3:n.5007G>C
ENST00000635804.1:n.465G>C
ENST00000635953.1:c.*453G>C	ENSP00000490058.1:n.*453G>C
ENST00000636155.1:c.838+3810G>C	ENSP00000490355.1:n.838+3810G>C
ENST00000636232.1:c.*817G>C	ENSP00000490325.1:n.*817G>C
ENST00000636754.1:c.*873G>C	ENSP00000489781.1:n.*873G>C
ENST00000636946.1:c.*1008-589G>C	ENSP00000490654.1:n.*1008-589G>C
ENST00000637037.1:c.*621G>C	ENSP00000490860.1:n.*621G>C
ENST00000637347.1:n.892G>C
ENST00000637611.1:c.*587G>C	ENSP00000489682.1:n.*587G>C
ENST00000637689.1:c.-341G>C	ENSP00000490496.1:n.-341G>C
ENST00000637925.1:c.*626G>C	ENSP00000489763.1:n.*626G>C
ENST00000638049.1:c.*789G>C	ENSP00000490597.1:n.*789G>C
ENST00000676175.1:n.2770G>C
ENST00000371413.4:c.839-589G>C	ENSP00000360467.3:n.839-589G>C
ENST00000371418.8:c.1031G>C	ENSP00000360472.4:p.Trp344Ser
ENST00000626307.1:n.4946G>C
ENST00000627420.2:c.*740G>C	ENSP00000487116.1:n.*740G>C
ENST00000629035.2:c.959G>C	ENSP00000486908.1:p.Trp320Ser
ENST00000630047.2:c.887G>C	ENSP00000485917.1:p.Trp296Ser
NM_001308275.1:c.839-589G>C	NP_001295204.1:n.839-589G>C
NM_001308276.1:c.887G>C	NP_001295205.1:p.Trp296Ser
NM_005097.2:c.1031G>C	NP_005088.1:p.Trp344Ser
NM_005097.3:c.1031G>C	NP_005088.1:p.Trp344Ser
NR_131777.1:n.1295G>C
XM_017016912.2:c.695-589G>C	XP_016872401.1:n.695-589G>C
NM_005097.4:c.1031G>C MANE Select	NP_005088.1:p.Trp344Ser
NM_001308275.2:c.839-589G>C	NP_001295204.1:n.839-589G>C
NM_001308276.2:c.887G>C	NP_001295205.1:p.Trp296Ser
NR_131777.2:n.1168G>C