Canonical Allele Identifier: CA377624405

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553064G>T (hg19) ; chr10:g.93793307G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793307G>T , CM000672.2:g.93793307G>T	GRCh38
NC_000010.10:g.95553064G>T , CM000672.1:g.95553064G>T	GRCh37
NC_000010.9:g.95543054G>T	NCBI36
NG_011832.1:g.40499G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.795G>T MANE Select	ENSP00000360472.4:p.Trp265Cys
ENST00000485458.3:n.4771G>T
ENST00000635953.1:c.795G>T	ENSP00000490058.1:p.Trp265Cys
ENST00000636155.1:c.795G>T	ENSP00000490355.1:p.Trp265Cys
ENST00000636232.1:c.*581G>T	ENSP00000490325.1:n.*581G>T
ENST00000636754.1:c.*637G>T	ENSP00000489781.1:n.*637G>T
ENST00000636946.1:c.*964G>T	ENSP00000490654.1:n.*964G>T
ENST00000637037.1:c.*385G>T	ENSP00000490860.1:n.*385G>T
ENST00000637347.1:n.656G>T
ENST00000637611.1:c.*351G>T	ENSP00000489682.1:n.*351G>T
ENST00000637689.1:c.-577G>T	ENSP00000490496.1:n.-577G>T
ENST00000637925.1:c.*390G>T	ENSP00000489763.1:n.*390G>T
ENST00000638049.1:c.*553G>T	ENSP00000490597.1:n.*553G>T
ENST00000676175.1:n.2534G>T
ENST00000371413.4:c.795G>T	ENSP00000360467.3:p.Trp265Cys
ENST00000371418.8:c.795G>T	ENSP00000360472.4:p.Trp265Cys
ENST00000626307.1:n.4710G>T
ENST00000626946.1:n.465G>T
ENST00000627420.2:c.*504G>T	ENSP00000487116.1:n.*504G>T
ENST00000629035.2:c.723G>T	ENSP00000486908.1:p.Trp241Cys
ENST00000630047.2:c.651G>T	ENSP00000485917.1:p.Trp217Cys
ENST00000630487.2:c.*585G>T	ENSP00000486859.1:n.*585G>T
NM_001308275.1:c.795G>T	NP_001295204.1:p.Trp265Cys
NM_001308276.1:c.651G>T	NP_001295205.1:p.Trp217Cys
NM_005097.2:c.795G>T	NP_005088.1:p.Trp265Cys
NM_005097.3:c.795G>T	NP_005088.1:p.Trp265Cys
NR_131777.1:n.1059G>T
XM_017016911.2:c.795G>T	XP_016872400.1:p.Trp265Cys
XM_017016912.2:c.651G>T	XP_016872401.1:p.Trp217Cys
NM_005097.4:c.795G>T MANE Select	NP_005088.1:p.Trp265Cys
NM_001308275.2:c.795G>T	NP_001295204.1:p.Trp265Cys
NM_001308276.2:c.651G>T	NP_001295205.1:p.Trp217Cys
NR_131777.2:n.932G>T