Canonical Allele Identifier: CA377624642

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553102T>C (hg19) ; chr10:g.93793345T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793345T>C , CM000672.2:g.93793345T>C	GRCh38
NC_000010.10:g.95553102T>C , CM000672.1:g.95553102T>C	GRCh37
NC_000010.9:g.95543092T>C	NCBI36
NG_011832.1:g.40537T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.833T>C MANE Select	ENSP00000360472.4:p.Ile278Thr
ENST00000485458.3:n.4809T>C
ENST00000635953.1:c.833T>C	ENSP00000490058.1:p.Ile278Thr
ENST00000636155.1:c.833T>C	ENSP00000490355.1:p.Ile278Thr
ENST00000636232.1:c.*619T>C	ENSP00000490325.1:n.*619T>C
ENST00000636754.1:c.*675T>C	ENSP00000489781.1:n.*675T>C
ENST00000636946.1:c.*1002T>C	ENSP00000490654.1:n.*1002T>C
ENST00000637037.1:c.*423T>C	ENSP00000490860.1:n.*423T>C
ENST00000637347.1:n.694T>C
ENST00000637611.1:c.*389T>C	ENSP00000489682.1:n.*389T>C
ENST00000637689.1:c.-539T>C	ENSP00000490496.1:n.-539T>C
ENST00000637925.1:c.*428T>C	ENSP00000489763.1:n.*428T>C
ENST00000638049.1:c.*591T>C	ENSP00000490597.1:n.*591T>C
ENST00000676175.1:n.2572T>C
ENST00000371413.4:c.833T>C	ENSP00000360467.3:p.Ile278Thr
ENST00000371418.8:c.833T>C	ENSP00000360472.4:p.Ile278Thr
ENST00000626307.1:n.4748T>C
ENST00000626946.1:n.503T>C
ENST00000627420.2:c.*542T>C	ENSP00000487116.1:n.*542T>C
ENST00000629035.2:c.761T>C	ENSP00000486908.1:p.Ile254Thr
ENST00000630047.2:c.689T>C	ENSP00000485917.1:p.Ile230Thr
ENST00000630487.2:c.*623T>C	ENSP00000486859.1:n.*623T>C
NM_001308275.1:c.833T>C	NP_001295204.1:p.Ile278Thr
NM_001308276.1:c.689T>C	NP_001295205.1:p.Ile230Thr
NM_005097.2:c.833T>C	NP_005088.1:p.Ile278Thr
NM_005097.3:c.833T>C	NP_005088.1:p.Ile278Thr
NR_131777.1:n.1097T>C
XM_017016911.2:c.833T>C	XP_016872400.1:p.Ile278Thr
XM_017016912.2:c.689T>C	XP_016872401.1:p.Ile230Thr
NM_005097.4:c.833T>C MANE Select	NP_005088.1:p.Ile278Thr
NM_001308275.2:c.833T>C	NP_001295204.1:p.Ile278Thr
NM_001308276.2:c.689T>C	NP_001295205.1:p.Ile230Thr
NR_131777.2:n.970T>C