Canonical Allele Identifier: CA931318576

Gene: LGI1

Linked Data

• dbSNP Id: rs117730565
• gnomAD v3: 10-93759016-A-G
• gnomAD v4: 10-93759016-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93759016A>G , CM000672.2:g.93759016A>G	GRCh38
NC_000010.10:g.95518773A>G , CM000672.1:g.95518773A>G	GRCh37
NC_000010.9:g.95508763A>G	NCBI36
NG_011832.1:g.6208A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+185A>G MANE Select	ENSP00000360472.4:n.287+185A>G
ENST00000635953.1:c.287+185A>G	ENSP00000490058.1:n.287+185A>G
ENST00000636140.1:n.72+185A>G
ENST00000636155.1:c.287+185A>G	ENSP00000490355.1:n.287+185A>G
ENST00000636232.1:c.*73+185A>G	ENSP00000490325.1:n.*73+185A>G
ENST00000636683.1:n.42+185A>G
ENST00000636754.1:c.*77+185A>G	ENSP00000489781.1:n.*77+185A>G
ENST00000636946.1:c.*181A>G	ENSP00000490654.1:n.*181A>G
ENST00000637037.1:c.287+185A>G	ENSP00000490860.1:n.287+185A>G
ENST00000637347.1:n.148+328A>G
ENST00000637611.1:c.287+185A>G	ENSP00000489682.1:n.287+185A>G
ENST00000637689.1:c.-1085+185A>G	ENSP00000490496.1:n.-1085+185A>G
ENST00000637925.1:c.287+185A>G	ENSP00000489763.1:n.287+185A>G
ENST00000638049.1:c.*45+185A>G	ENSP00000490597.1:n.*45+185A>G
ENST00000371413.4:c.287+185A>G	ENSP00000360467.3:n.287+185A>G
ENST00000371418.8:c.287+185A>G	ENSP00000360472.4:n.287+185A>G
ENST00000627420.2:c.*77+185A>G	ENSP00000487116.1:n.*77+185A>G
ENST00000627699.1:c.*262A>G	ENSP00000485868.1:n.*262A>G
ENST00000629035.2:c.215+657A>G	ENSP00000486908.1:n.215+657A>G
ENST00000630047.2:c.287+185A>G	ENSP00000485917.1:n.287+185A>G
ENST00000630184.2:c.287+185A>G	ENSP00000486607.1:n.287+185A>G
ENST00000630487.2:c.*77+185A>G	ENSP00000486859.1:n.*77+185A>G
NM_001308275.1:c.287+185A>G	NP_001295204.1:n.287+185A>G
NM_001308276.1:c.287+185A>G	NP_001295205.1:n.287+185A>G
NM_005097.2:c.287+185A>G	NP_005088.1:n.287+185A>G
NM_005097.3:c.287+185A>G	NP_005088.1:n.287+185A>G
NR_131777.1:n.632+185A>G
XM_017016911.2:c.287+185A>G	XP_016872400.1:n.287+185A>G
XM_017016912.2:c.287+185A>G	XP_016872401.1:n.287+185A>G
XR_001747552.1:n.4859T>C
XR_002957095.1:n.6987T>C
XR_002957096.1:n.8199T>C
NM_005097.4:c.287+185A>G MANE Select	NP_005088.1:n.287+185A>G
NM_001308275.2:c.287+185A>G	NP_001295204.1:n.287+185A>G
NM_001308276.2:c.287+185A>G	NP_001295205.1:n.287+185A>G
NR_131777.2:n.505+185A>G