Canonical Allele Identifier: CA377627909

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557025C>G (hg19) ; chr10:g.93797268C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797268C>G , CM000672.2:g.93797268C>G	GRCh38
NC_000010.10:g.95557025C>G , CM000672.1:g.95557025C>G	GRCh37
NC_000010.9:g.95547015C>G	NCBI36
NG_011832.1:g.44460C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1139C>G MANE Select	ENSP00000360472.4:p.Thr380Ser
ENST00000485458.3:n.5115C>G
ENST00000635804.1:n.573C>G
ENST00000635953.1:c.*561C>G	ENSP00000490058.1:n.*561C>G
ENST00000636155.1:c.838+3918C>G	ENSP00000490355.1:n.838+3918C>G
ENST00000636232.1:c.*925C>G	ENSP00000490325.1:n.*925C>G
ENST00000636754.1:c.*981C>G	ENSP00000489781.1:n.*981C>G
ENST00000636946.1:c.*1008-481C>G	ENSP00000490654.1:n.*1008-481C>G
ENST00000637037.1:c.*729C>G	ENSP00000490860.1:n.*729C>G
ENST00000637347.1:n.1000C>G
ENST00000637611.1:c.*695C>G	ENSP00000489682.1:n.*695C>G
ENST00000637689.1:c.-233C>G	ENSP00000490496.1:n.-233C>G
ENST00000637925.1:c.*734C>G	ENSP00000489763.1:n.*734C>G
ENST00000638049.1:c.*897C>G	ENSP00000490597.1:n.*897C>G
ENST00000676175.1:n.2878C>G
ENST00000371413.4:c.839-481C>G	ENSP00000360467.3:n.839-481C>G
ENST00000371418.8:c.1139C>G	ENSP00000360472.4:p.Thr380Ser
ENST00000626307.1:n.5054C>G
ENST00000627420.2:c.*848C>G	ENSP00000487116.1:n.*848C>G
ENST00000629035.2:c.1067C>G	ENSP00000486908.1:p.Thr356Ser
ENST00000630047.2:c.995C>G	ENSP00000485917.1:p.Thr332Ser
NM_001308275.1:c.839-481C>G	NP_001295204.1:n.839-481C>G
NM_001308276.1:c.995C>G	NP_001295205.1:p.Thr332Ser
NM_005097.2:c.1139C>G	NP_005088.1:p.Thr380Ser
NM_005097.3:c.1139C>G	NP_005088.1:p.Thr380Ser
NR_131777.1:n.1403C>G
XM_017016912.2:c.695-481C>G	XP_016872401.1:n.695-481C>G
NM_005097.4:c.1139C>G MANE Select	NP_005088.1:p.Thr380Ser
NM_001308275.2:c.839-481C>G	NP_001295204.1:n.839-481C>G
NM_001308276.2:c.995C>G	NP_001295205.1:p.Thr332Ser
NR_131777.2:n.1276C>G