Canonical Allele Identifier: CA377623926

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552955C>G (hg19) ; chr10:g.93793198C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793198C>G , CM000672.2:g.93793198C>G	GRCh38
NC_000010.10:g.95552955C>G , CM000672.1:g.95552955C>G	GRCh37
NC_000010.9:g.95542945C>G	NCBI36
NG_011832.1:g.40390C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.686C>G MANE Select	ENSP00000360472.4:p.Ser229Cys
ENST00000485458.3:n.4662C>G
ENST00000635953.1:c.686C>G	ENSP00000490058.1:p.Ser229Cys
ENST00000636155.1:c.686C>G	ENSP00000490355.1:p.Ser229Cys
ENST00000636232.1:c.*472C>G	ENSP00000490325.1:n.*472C>G
ENST00000636754.1:c.*528C>G	ENSP00000489781.1:n.*528C>G
ENST00000636946.1:c.*855C>G	ENSP00000490654.1:n.*855C>G
ENST00000637037.1:c.*276C>G	ENSP00000490860.1:n.*276C>G
ENST00000637347.1:n.547C>G
ENST00000637611.1:c.*242C>G	ENSP00000489682.1:n.*242C>G
ENST00000637689.1:c.-686C>G	ENSP00000490496.1:n.-686C>G
ENST00000637925.1:c.*281C>G	ENSP00000489763.1:n.*281C>G
ENST00000638049.1:c.*444C>G	ENSP00000490597.1:n.*444C>G
ENST00000676175.1:n.2425C>G
ENST00000371413.4:c.686C>G	ENSP00000360467.3:p.Ser229Cys
ENST00000371418.8:c.686C>G	ENSP00000360472.4:p.Ser229Cys
ENST00000626307.1:n.4601C>G
ENST00000626946.1:n.356C>G
ENST00000627420.2:c.*395C>G	ENSP00000487116.1:n.*395C>G
ENST00000629035.2:c.614C>G	ENSP00000486908.1:p.Ser205Cys
ENST00000630047.2:c.542C>G	ENSP00000485917.1:p.Ser181Cys
ENST00000630412.1:n.474C>G
ENST00000630487.2:c.*476C>G	ENSP00000486859.1:n.*476C>G
NM_001308275.1:c.686C>G	NP_001295204.1:p.Ser229Cys
NM_001308276.1:c.542C>G	NP_001295205.1:p.Ser181Cys
NM_005097.2:c.686C>G	NP_005088.1:p.Ser229Cys
NM_005097.3:c.686C>G	NP_005088.1:p.Ser229Cys
NR_131777.1:n.950C>G
XM_017016911.2:c.686C>G	XP_016872400.1:p.Ser229Cys
XM_017016912.2:c.542C>G	XP_016872401.1:p.Ser181Cys
NM_005097.4:c.686C>G MANE Select	NP_005088.1:p.Ser229Cys
NM_001308275.2:c.686C>G	NP_001295204.1:p.Ser229Cys
NM_001308276.2:c.542C>G	NP_001295205.1:p.Ser181Cys
NR_131777.2:n.823C>G