Canonical Allele Identifier: CA377627214

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556921C>A (hg19) ; chr10:g.93797164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797164C>A , CM000672.2:g.93797164C>A	GRCh38
NC_000010.10:g.95556921C>A , CM000672.1:g.95556921C>A	GRCh37
NC_000010.9:g.95546911C>A	NCBI36
NG_011832.1:g.44356C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1035C>A MANE Select	ENSP00000360472.4:p.Tyr345Ter
ENST00000485458.3:n.5011C>A
ENST00000635804.1:n.469C>A
ENST00000635953.1:c.*457C>A	ENSP00000490058.1:n.*457C>A
ENST00000636155.1:c.838+3814C>A	ENSP00000490355.1:n.838+3814C>A
ENST00000636232.1:c.*821C>A	ENSP00000490325.1:n.*821C>A
ENST00000636754.1:c.*877C>A	ENSP00000489781.1:n.*877C>A
ENST00000636946.1:c.*1008-585C>A	ENSP00000490654.1:n.*1008-585C>A
ENST00000637037.1:c.*625C>A	ENSP00000490860.1:n.*625C>A
ENST00000637347.1:n.896C>A
ENST00000637611.1:c.*591C>A	ENSP00000489682.1:n.*591C>A
ENST00000637689.1:c.-337C>A	ENSP00000490496.1:n.-337C>A
ENST00000637925.1:c.*630C>A	ENSP00000489763.1:n.*630C>A
ENST00000638049.1:c.*793C>A	ENSP00000490597.1:n.*793C>A
ENST00000676175.1:n.2774C>A
ENST00000371413.4:c.839-585C>A	ENSP00000360467.3:n.839-585C>A
ENST00000371418.8:c.1035C>A	ENSP00000360472.4:p.Tyr345Ter
ENST00000626307.1:n.4950C>A
ENST00000627420.2:c.*744C>A	ENSP00000487116.1:n.*744C>A
ENST00000629035.2:c.963C>A	ENSP00000486908.1:p.Tyr321Ter
ENST00000630047.2:c.891C>A	ENSP00000485917.1:p.Tyr297Ter
NM_001308275.1:c.839-585C>A	NP_001295204.1:n.839-585C>A
NM_001308276.1:c.891C>A	NP_001295205.1:p.Tyr297Ter
NM_005097.2:c.1035C>A	NP_005088.1:p.Tyr345Ter
NM_005097.3:c.1035C>A	NP_005088.1:p.Tyr345Ter
NR_131777.1:n.1299C>A
XM_017016912.2:c.695-585C>A	XP_016872401.1:n.695-585C>A
NM_005097.4:c.1035C>A MANE Select	NP_005088.1:p.Tyr345Ter
NM_001308275.2:c.839-585C>A	NP_001295204.1:n.839-585C>A
NM_001308276.2:c.891C>A	NP_001295205.1:p.Tyr297Ter
NR_131777.2:n.1172C>A