Canonical Allele Identifier: CA377626174

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556740T>C (hg19) ; chr10:g.93796983T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93796983T>C , CM000672.2:g.93796983T>C	GRCh38
NC_000010.10:g.95556740T>C , CM000672.1:g.95556740T>C	GRCh37
NC_000010.9:g.95546730T>C	NCBI36
NG_011832.1:g.44175T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.854T>C MANE Select	ENSP00000360472.4:p.Val285Ala
ENST00000485458.3:n.4830T>C
ENST00000635804.1:n.288T>C
ENST00000635953.1:c.*276T>C	ENSP00000490058.1:n.*276T>C
ENST00000636155.1:c.838+3633T>C	ENSP00000490355.1:n.838+3633T>C
ENST00000636232.1:c.*640T>C	ENSP00000490325.1:n.*640T>C
ENST00000636754.1:c.*696T>C	ENSP00000489781.1:n.*696T>C
ENST00000636946.1:c.*1008-766T>C	ENSP00000490654.1:n.*1008-766T>C
ENST00000637037.1:c.*444T>C	ENSP00000490860.1:n.*444T>C
ENST00000637347.1:n.715T>C
ENST00000637611.1:c.*410T>C	ENSP00000489682.1:n.*410T>C
ENST00000637689.1:c.-518T>C	ENSP00000490496.1:n.-518T>C
ENST00000637925.1:c.*449T>C	ENSP00000489763.1:n.*449T>C
ENST00000638049.1:c.*612T>C	ENSP00000490597.1:n.*612T>C
ENST00000676175.1:n.2593T>C
ENST00000371413.4:c.839-766T>C	ENSP00000360467.3:n.839-766T>C
ENST00000371418.8:c.854T>C	ENSP00000360472.4:p.Val285Ala
ENST00000626307.1:n.4769T>C
ENST00000626946.1:n.524T>C
ENST00000627420.2:c.*563T>C	ENSP00000487116.1:n.*563T>C
ENST00000629035.2:c.782T>C	ENSP00000486908.1:p.Val261Ala
ENST00000630047.2:c.710T>C	ENSP00000485917.1:p.Val237Ala
NM_001308275.1:c.839-766T>C	NP_001295204.1:n.839-766T>C
NM_001308276.1:c.710T>C	NP_001295205.1:p.Val237Ala
NM_005097.2:c.854T>C	NP_005088.1:p.Val285Ala
NM_005097.3:c.854T>C	NP_005088.1:p.Val285Ala
NR_131777.1:n.1118T>C
XM_017016912.2:c.695-766T>C	XP_016872401.1:n.695-766T>C
NM_005097.4:c.854T>C MANE Select	NP_005088.1:p.Val285Ala
NM_001308275.2:c.839-766T>C	NP_001295204.1:n.839-766T>C
NM_001308276.2:c.710T>C	NP_001295205.1:p.Val237Ala
NR_131777.2:n.991T>C