Canonical Allele Identifier: CA377624014

Gene: LGI1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.707C>T MANE Select	ENSP00000360472.4:p.Ser236Leu
ENST00000485458.3:n.4683C>T
ENST00000635953.1:c.707C>T	ENSP00000490058.1:p.Ser236Leu
ENST00000636155.1:c.707C>T	ENSP00000490355.1:p.Ser236Leu
ENST00000636232.1:c.*493C>T	ENSP00000490325.1:n.*493C>T
ENST00000636754.1:c.*549C>T	ENSP00000489781.1:n.*549C>T
ENST00000636946.1:c.*876C>T	ENSP00000490654.1:n.*876C>T
ENST00000637037.1:c.*297C>T	ENSP00000490860.1:n.*297C>T
ENST00000637347.1:n.568C>T
ENST00000637611.1:c.*263C>T	ENSP00000489682.1:n.*263C>T
ENST00000637689.1:c.-665C>T	ENSP00000490496.1:n.-665C>T
ENST00000637925.1:c.*302C>T	ENSP00000489763.1:n.*302C>T
ENST00000638049.1:c.*465C>T	ENSP00000490597.1:n.*465C>T
ENST00000676175.1:n.2446C>T
ENST00000371413.4:c.707C>T	ENSP00000360467.3:p.Ser236Leu
ENST00000371418.8:c.707C>T	ENSP00000360472.4:p.Ser236Leu
ENST00000626307.1:n.4622C>T
ENST00000626946.1:n.377C>T
ENST00000627420.2:c.*416C>T	ENSP00000487116.1:n.*416C>T
ENST00000629035.2:c.635C>T	ENSP00000486908.1:p.Ser212Leu
ENST00000630047.2:c.563C>T	ENSP00000485917.1:p.Ser188Leu
ENST00000630412.1:n.495C>T
ENST00000630487.2:c.*497C>T	ENSP00000486859.1:n.*497C>T
NM_001308275.1:c.707C>T	NP_001295204.1:p.Ser236Leu
NM_001308276.1:c.563C>T	NP_001295205.1:p.Ser188Leu
NM_005097.2:c.707C>T	NP_005088.1:p.Ser236Leu
NM_005097.3:c.707C>T	NP_005088.1:p.Ser236Leu
NR_131777.1:n.971C>T
XM_017016911.2:c.707C>T	XP_016872400.1:p.Ser236Leu
XM_017016912.2:c.563C>T	XP_016872401.1:p.Ser188Leu
NM_005097.4:c.707C>T MANE Select	NP_005088.1:p.Ser236Leu
NM_001308275.2:c.707C>T	NP_001295204.1:p.Ser236Leu
NM_001308276.2:c.563C>T	NP_001295205.1:p.Ser188Leu
NR_131777.2:n.844C>T