Canonical Allele Identifier: CA377624025

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552980G>C (hg19) ; chr10:g.93793223G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793223G>C , CM000672.2:g.93793223G>C	GRCh38
NC_000010.10:g.95552980G>C , CM000672.1:g.95552980G>C	GRCh37
NC_000010.9:g.95542970G>C	NCBI36
NG_011832.1:g.40415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.711G>C MANE Select	ENSP00000360472.4:p.Leu237Phe
ENST00000485458.3:n.4687G>C
ENST00000635953.1:c.711G>C	ENSP00000490058.1:p.Leu237Phe
ENST00000636155.1:c.711G>C	ENSP00000490355.1:p.Leu237Phe
ENST00000636232.1:c.*497G>C	ENSP00000490325.1:n.*497G>C
ENST00000636754.1:c.*553G>C	ENSP00000489781.1:n.*553G>C
ENST00000636946.1:c.*880G>C	ENSP00000490654.1:n.*880G>C
ENST00000637037.1:c.*301G>C	ENSP00000490860.1:n.*301G>C
ENST00000637347.1:n.572G>C
ENST00000637611.1:c.*267G>C	ENSP00000489682.1:n.*267G>C
ENST00000637689.1:c.-661G>C	ENSP00000490496.1:n.-661G>C
ENST00000637925.1:c.*306G>C	ENSP00000489763.1:n.*306G>C
ENST00000638049.1:c.*469G>C	ENSP00000490597.1:n.*469G>C
ENST00000676175.1:n.2450G>C
ENST00000371413.4:c.711G>C	ENSP00000360467.3:p.Leu237Phe
ENST00000371418.8:c.711G>C	ENSP00000360472.4:p.Leu237Phe
ENST00000626307.1:n.4626G>C
ENST00000626946.1:n.381G>C
ENST00000627420.2:c.*420G>C	ENSP00000487116.1:n.*420G>C
ENST00000629035.2:c.639G>C	ENSP00000486908.1:p.Leu213Phe
ENST00000630047.2:c.567G>C	ENSP00000485917.1:p.Leu189Phe
ENST00000630412.1:n.499G>C
ENST00000630487.2:c.*501G>C	ENSP00000486859.1:n.*501G>C
NM_001308275.1:c.711G>C	NP_001295204.1:p.Leu237Phe
NM_001308276.1:c.567G>C	NP_001295205.1:p.Leu189Phe
NM_005097.2:c.711G>C	NP_005088.1:p.Leu237Phe
NM_005097.3:c.711G>C	NP_005088.1:p.Leu237Phe
NR_131777.1:n.975G>C
XM_017016911.2:c.711G>C	XP_016872400.1:p.Leu237Phe
XM_017016912.2:c.567G>C	XP_016872401.1:p.Leu189Phe
NM_005097.4:c.711G>C MANE Select	NP_005088.1:p.Leu237Phe
NM_001308275.2:c.711G>C	NP_001295204.1:p.Leu237Phe
NM_001308276.2:c.567G>C	NP_001295205.1:p.Leu189Phe
NR_131777.2:n.848G>C