Canonical Allele Identifier: CA377624011

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552976C>A (hg19) ; chr10:g.93793219C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793219C>A , CM000672.2:g.93793219C>A	GRCh38
NC_000010.10:g.95552976C>A , CM000672.1:g.95552976C>A	GRCh37
NC_000010.9:g.95542966C>A	NCBI36
NG_011832.1:g.40411C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.707C>A MANE Select	ENSP00000360472.4:p.Ser236Ter
ENST00000485458.3:n.4683C>A
ENST00000635953.1:c.707C>A	ENSP00000490058.1:p.Ser236Ter
ENST00000636155.1:c.707C>A	ENSP00000490355.1:p.Ser236Ter
ENST00000636232.1:c.*493C>A	ENSP00000490325.1:n.*493C>A
ENST00000636754.1:c.*549C>A	ENSP00000489781.1:n.*549C>A
ENST00000636946.1:c.*876C>A	ENSP00000490654.1:n.*876C>A
ENST00000637037.1:c.*297C>A	ENSP00000490860.1:n.*297C>A
ENST00000637347.1:n.568C>A
ENST00000637611.1:c.*263C>A	ENSP00000489682.1:n.*263C>A
ENST00000637689.1:c.-665C>A	ENSP00000490496.1:n.-665C>A
ENST00000637925.1:c.*302C>A	ENSP00000489763.1:n.*302C>A
ENST00000638049.1:c.*465C>A	ENSP00000490597.1:n.*465C>A
ENST00000676175.1:n.2446C>A
ENST00000371413.4:c.707C>A	ENSP00000360467.3:p.Ser236Ter
ENST00000371418.8:c.707C>A	ENSP00000360472.4:p.Ser236Ter
ENST00000626307.1:n.4622C>A
ENST00000626946.1:n.377C>A
ENST00000627420.2:c.*416C>A	ENSP00000487116.1:n.*416C>A
ENST00000629035.2:c.635C>A	ENSP00000486908.1:p.Ser212Ter
ENST00000630047.2:c.563C>A	ENSP00000485917.1:p.Ser188Ter
ENST00000630412.1:n.495C>A
ENST00000630487.2:c.*497C>A	ENSP00000486859.1:n.*497C>A
NM_001308275.1:c.707C>A	NP_001295204.1:p.Ser236Ter
NM_001308276.1:c.563C>A	NP_001295205.1:p.Ser188Ter
NM_005097.2:c.707C>A	NP_005088.1:p.Ser236Ter
NM_005097.3:c.707C>A	NP_005088.1:p.Ser236Ter
NR_131777.1:n.971C>A
XM_017016911.2:c.707C>A	XP_016872400.1:p.Ser236Ter
XM_017016912.2:c.563C>A	XP_016872401.1:p.Ser188Ter
NM_005097.4:c.707C>A MANE Select	NP_005088.1:p.Ser236Ter
NM_001308275.2:c.707C>A	NP_001295204.1:p.Ser236Ter
NM_001308276.2:c.563C>A	NP_001295205.1:p.Ser188Ter
NR_131777.2:n.844C>A