Canonical Allele Identifier: CA211583611

Gene: LGI1

Linked Data

• dbSNP Id: rs182125354
• gnomAD v3: 10-93793074-A-G
• gnomAD v4: 10-93793074-A-G
• MyVariant Identifiers: chr10:g.95552831A>G (hg19) ; chr10:g.93793074A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793074A>G , CM000672.2:g.93793074A>G	GRCh38
NC_000010.10:g.95552831A>G , CM000672.1:g.95552831A>G	GRCh37
NC_000010.9:g.95542821A>G	NCBI36
NG_011832.1:g.40266A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.674-112A>G MANE Select	ENSP00000360472.4:n.674-112A>G
ENST00000485458.3:n.4650-112A>G
ENST00000635953.1:c.674-112A>G	ENSP00000490058.1:n.674-112A>G
ENST00000636155.1:c.674-112A>G	ENSP00000490355.1:n.674-112A>G
ENST00000636232.1:c.*460-112A>G	ENSP00000490325.1:n.*460-112A>G
ENST00000636754.1:c.*516-112A>G	ENSP00000489781.1:n.*516-112A>G
ENST00000636946.1:c.*843-112A>G	ENSP00000490654.1:n.*843-112A>G
ENST00000637037.1:c.*264-112A>G	ENSP00000490860.1:n.*264-112A>G
ENST00000637347.1:n.535-112A>G
ENST00000637611.1:c.*230-112A>G	ENSP00000489682.1:n.*230-112A>G
ENST00000637689.1:c.-698-112A>G	ENSP00000490496.1:n.-698-112A>G
ENST00000637925.1:c.*269-112A>G	ENSP00000489763.1:n.*269-112A>G
ENST00000638049.1:c.*432-112A>G	ENSP00000490597.1:n.*432-112A>G
ENST00000676175.1:n.2413-112A>G
ENST00000371413.4:c.674-112A>G	ENSP00000360467.3:n.674-112A>G
ENST00000371418.8:c.674-112A>G	ENSP00000360472.4:n.674-112A>G
ENST00000626307.1:n.4589-112A>G
ENST00000626946.1:n.232A>G
ENST00000627420.2:c.*383-112A>G	ENSP00000487116.1:n.*383-112A>G
ENST00000629035.2:c.602-112A>G	ENSP00000486908.1:n.602-112A>G
ENST00000630047.2:c.530-112A>G	ENSP00000485917.1:n.530-112A>G
ENST00000630412.1:n.462-112A>G
ENST00000630487.2:c.*464-112A>G	ENSP00000486859.1:n.*464-112A>G
NM_001308275.1:c.674-112A>G	NP_001295204.1:n.674-112A>G
NM_001308276.1:c.530-112A>G	NP_001295205.1:n.530-112A>G
NM_005097.2:c.674-112A>G	NP_005088.1:n.674-112A>G
NM_005097.3:c.674-112A>G	NP_005088.1:n.674-112A>G
NR_131777.1:n.938-112A>G
XM_017016911.2:c.674-112A>G	XP_016872400.1:n.674-112A>G
XM_017016912.2:c.530-112A>G	XP_016872401.1:n.530-112A>G
NM_005097.4:c.674-112A>G MANE Select	NP_005088.1:n.674-112A>G
NM_001308275.2:c.674-112A>G	NP_001295204.1:n.674-112A>G
NM_001308276.2:c.530-112A>G	NP_001295205.1:n.530-112A>G
NR_131777.2:n.811-112A>G