Canonical Allele Identifier: CA377626732

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556848T>G (hg19) ; chr10:g.93797091T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797091T>G , CM000672.2:g.93797091T>G	GRCh38
NC_000010.10:g.95556848T>G , CM000672.1:g.95556848T>G	GRCh37
NC_000010.9:g.95546838T>G	NCBI36
NG_011832.1:g.44283T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.962T>G MANE Select	ENSP00000360472.4:p.Ile321Ser
ENST00000485458.3:n.4938T>G
ENST00000635804.1:n.396T>G
ENST00000635953.1:c.*384T>G	ENSP00000490058.1:n.*384T>G
ENST00000636155.1:c.838+3741T>G	ENSP00000490355.1:n.838+3741T>G
ENST00000636232.1:c.*748T>G	ENSP00000490325.1:n.*748T>G
ENST00000636754.1:c.*804T>G	ENSP00000489781.1:n.*804T>G
ENST00000636946.1:c.*1008-658T>G	ENSP00000490654.1:n.*1008-658T>G
ENST00000637037.1:c.*552T>G	ENSP00000490860.1:n.*552T>G
ENST00000637347.1:n.823T>G
ENST00000637611.1:c.*518T>G	ENSP00000489682.1:n.*518T>G
ENST00000637689.1:c.-410T>G	ENSP00000490496.1:n.-410T>G
ENST00000637925.1:c.*557T>G	ENSP00000489763.1:n.*557T>G
ENST00000638049.1:c.*720T>G	ENSP00000490597.1:n.*720T>G
ENST00000676175.1:n.2701T>G
ENST00000371413.4:c.839-658T>G	ENSP00000360467.3:n.839-658T>G
ENST00000371418.8:c.962T>G	ENSP00000360472.4:p.Ile321Ser
ENST00000626307.1:n.4877T>G
ENST00000627420.2:c.*671T>G	ENSP00000487116.1:n.*671T>G
ENST00000629035.2:c.890T>G	ENSP00000486908.1:p.Ile297Ser
ENST00000630047.2:c.818T>G	ENSP00000485917.1:p.Ile273Ser
NM_001308275.1:c.839-658T>G	NP_001295204.1:n.839-658T>G
NM_001308276.1:c.818T>G	NP_001295205.1:p.Ile273Ser
NM_005097.2:c.962T>G	NP_005088.1:p.Ile321Ser
NM_005097.3:c.962T>G	NP_005088.1:p.Ile321Ser
NR_131777.1:n.1226T>G
XM_017016912.2:c.695-658T>G	XP_016872401.1:n.695-658T>G
NM_005097.4:c.962T>G MANE Select	NP_005088.1:p.Ile321Ser
NM_001308275.2:c.839-658T>G	NP_001295204.1:n.839-658T>G
NM_001308276.2:c.818T>G	NP_001295205.1:p.Ile273Ser
NR_131777.2:n.1099T>G