Canonical Allele Identifier: CA377627895

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557024A>G (hg19) ; chr10:g.93797267A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797267A>G , CM000672.2:g.93797267A>G	GRCh38
NC_000010.10:g.95557024A>G , CM000672.1:g.95557024A>G	GRCh37
NC_000010.9:g.95547014A>G	NCBI36
NG_011832.1:g.44459A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1138A>G MANE Select	ENSP00000360472.4:p.Thr380Ala
ENST00000485458.3:n.5114A>G
ENST00000635804.1:n.572A>G
ENST00000635953.1:c.*560A>G	ENSP00000490058.1:n.*560A>G
ENST00000636155.1:c.838+3917A>G	ENSP00000490355.1:n.838+3917A>G
ENST00000636232.1:c.*924A>G	ENSP00000490325.1:n.*924A>G
ENST00000636754.1:c.*980A>G	ENSP00000489781.1:n.*980A>G
ENST00000636946.1:c.*1008-482A>G	ENSP00000490654.1:n.*1008-482A>G
ENST00000637037.1:c.*728A>G	ENSP00000490860.1:n.*728A>G
ENST00000637347.1:n.999A>G
ENST00000637611.1:c.*694A>G	ENSP00000489682.1:n.*694A>G
ENST00000637689.1:c.-234A>G	ENSP00000490496.1:n.-234A>G
ENST00000637925.1:c.*733A>G	ENSP00000489763.1:n.*733A>G
ENST00000638049.1:c.*896A>G	ENSP00000490597.1:n.*896A>G
ENST00000676175.1:n.2877A>G
ENST00000371413.4:c.839-482A>G	ENSP00000360467.3:n.839-482A>G
ENST00000371418.8:c.1138A>G	ENSP00000360472.4:p.Thr380Ala
ENST00000626307.1:n.5053A>G
ENST00000627420.2:c.*847A>G	ENSP00000487116.1:n.*847A>G
ENST00000629035.2:c.1066A>G	ENSP00000486908.1:p.Thr356Ala
ENST00000630047.2:c.994A>G	ENSP00000485917.1:p.Thr332Ala
NM_001308275.1:c.839-482A>G	NP_001295204.1:n.839-482A>G
NM_001308276.1:c.994A>G	NP_001295205.1:p.Thr332Ala
NM_005097.2:c.1138A>G	NP_005088.1:p.Thr380Ala
NM_005097.3:c.1138A>G	NP_005088.1:p.Thr380Ala
NR_131777.1:n.1402A>G
XM_017016912.2:c.695-482A>G	XP_016872401.1:n.695-482A>G
NM_005097.4:c.1138A>G MANE Select	NP_005088.1:p.Thr380Ala
NM_001308275.2:c.839-482A>G	NP_001295204.1:n.839-482A>G
NM_001308276.2:c.994A>G	NP_001295205.1:p.Thr332Ala
NR_131777.2:n.1275A>G