Canonical Allele Identifier: CA377628557

Gene: LGI1

Linked Data

• dbSNP Id: rs2059989772
• gnomAD v3: 10-93797370-A-G
• gnomAD v4: 10-93797370-A-G
• MyVariant Identifiers: chr10:g.95557127A>G (hg19) ; chr10:g.93797370A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797370A>G , CM000672.2:g.93797370A>G	GRCh38
NC_000010.10:g.95557127A>G , CM000672.1:g.95557127A>G	GRCh37
NC_000010.9:g.95547117A>G	NCBI36
NG_011832.1:g.44562A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1241A>G MANE Select	ENSP00000360472.4:p.Asn414Ser
ENST00000485458.3:n.5217A>G
ENST00000635804.1:n.675A>G
ENST00000635953.1:c.*663A>G	ENSP00000490058.1:n.*663A>G
ENST00000636155.1:c.838+4020A>G	ENSP00000490355.1:n.838+4020A>G
ENST00000636232.1:c.*1027A>G	ENSP00000490325.1:n.*1027A>G
ENST00000636754.1:c.*1083A>G	ENSP00000489781.1:n.*1083A>G
ENST00000636946.1:c.*1008-379A>G	ENSP00000490654.1:n.*1008-379A>G
ENST00000637037.1:c.*831A>G	ENSP00000490860.1:n.*831A>G
ENST00000637347.1:n.1102A>G
ENST00000637611.1:c.*797A>G	ENSP00000489682.1:n.*797A>G
ENST00000637689.1:c.-131A>G	ENSP00000490496.1:n.-131A>G
ENST00000637925.1:c.*836A>G	ENSP00000489763.1:n.*836A>G
ENST00000638049.1:c.*999A>G	ENSP00000490597.1:n.*999A>G
ENST00000676175.1:n.2980A>G
ENST00000371413.4:c.839-379A>G	ENSP00000360467.3:n.839-379A>G
ENST00000371418.8:c.1241A>G	ENSP00000360472.4:p.Asn414Ser
ENST00000626307.1:n.5156A>G
ENST00000627420.2:c.*950A>G	ENSP00000487116.1:n.*950A>G
ENST00000629035.2:c.1169A>G	ENSP00000486908.1:p.Asn390Ser
ENST00000630047.2:c.1097A>G	ENSP00000485917.1:p.Asn366Ser
NM_001308275.1:c.839-379A>G	NP_001295204.1:n.839-379A>G
NM_001308276.1:c.1097A>G	NP_001295205.1:p.Asn366Ser
NM_005097.2:c.1241A>G	NP_005088.1:p.Asn414Ser
NM_005097.3:c.1241A>G	NP_005088.1:p.Asn414Ser
NR_131777.1:n.1505A>G
XM_017016912.2:c.695-379A>G	XP_016872401.1:n.695-379A>G
NM_005097.4:c.1241A>G MANE Select	NP_005088.1:p.Asn414Ser
NM_001308275.2:c.839-379A>G	NP_001295204.1:n.839-379A>G
NM_001308276.2:c.1097A>G	NP_001295205.1:p.Asn366Ser
NR_131777.2:n.1378A>G