Canonical Allele Identifier: CA377624670

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553107G>C (hg19) ; chr10:g.93793350G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793350G>C , CM000672.2:g.93793350G>C	GRCh38
NC_000010.10:g.95553107G>C , CM000672.1:g.95553107G>C	GRCh37
NC_000010.9:g.95543097G>C	NCBI36
NG_011832.1:g.40542G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.838G>C MANE Select	ENSP00000360472.4:p.Gly280Arg
ENST00000485458.3:n.4814G>C
ENST00000635953.1:c.838G>C	ENSP00000490058.1:p.Gly280Arg
ENST00000636155.1:c.838G>C	ENSP00000490355.1:p.Gly280Arg
ENST00000636232.1:c.*624G>C	ENSP00000490325.1:n.*624G>C
ENST00000636754.1:c.*680G>C	ENSP00000489781.1:n.*680G>C
ENST00000636946.1:c.*1007G>C	ENSP00000490654.1:n.*1007G>C
ENST00000637037.1:c.*428G>C	ENSP00000490860.1:n.*428G>C
ENST00000637347.1:n.699G>C
ENST00000637611.1:c.*394G>C	ENSP00000489682.1:n.*394G>C
ENST00000637689.1:c.-534G>C	ENSP00000490496.1:n.-534G>C
ENST00000637925.1:c.*433G>C	ENSP00000489763.1:n.*433G>C
ENST00000638049.1:c.*596G>C	ENSP00000490597.1:n.*596G>C
ENST00000676175.1:n.2577G>C
ENST00000371413.4:c.838G>C	ENSP00000360467.3:p.Val280Leu
ENST00000371418.8:c.838G>C	ENSP00000360472.4:p.Gly280Arg
ENST00000626307.1:n.4753G>C
ENST00000626946.1:n.508G>C
ENST00000627420.2:c.*547G>C	ENSP00000487116.1:n.*547G>C
ENST00000629035.2:c.766G>C	ENSP00000486908.1:p.Gly256Arg
ENST00000630047.2:c.694G>C	ENSP00000485917.1:p.Gly232Arg
NM_001308275.1:c.838G>C	NP_001295204.1:p.Val280Leu
NM_001308276.1:c.694G>C	NP_001295205.1:p.Gly232Arg
NM_005097.2:c.838G>C	NP_005088.1:p.Gly280Arg
NM_005097.3:c.838G>C	NP_005088.1:p.Gly280Arg
NR_131777.1:n.1102G>C
XM_017016911.2:c.838G>C	XP_016872400.1:p.Gly280Arg
XM_017016912.2:c.694G>C	XP_016872401.1:p.Val232Leu
NM_005097.4:c.838G>C MANE Select	NP_005088.1:p.Gly280Arg
NM_001308275.2:c.838G>C	NP_001295204.1:p.Val280Leu
NM_001308276.2:c.694G>C	NP_001295205.1:p.Gly232Arg
NR_131777.2:n.975G>C