Canonical Allele Identifier: CA470800119

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553034T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793277T>A , CM000672.2:g.93793277T>A	GRCh38
NC_000010.10:g.95553034T>A , CM000672.1:g.95553034T>A	GRCh37
NC_000010.9:g.95543024T>A	NCBI36
NG_011832.1:g.40469T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.765T>A MANE Select	ENSP00000360472.4:p.Pro255=
ENST00000485458.3:n.4741T>A
ENST00000635953.1:c.765T>A	ENSP00000490058.1:p.Pro255=
ENST00000636155.1:c.765T>A	ENSP00000490355.1:p.Pro255=
ENST00000636232.1:c.*551T>A	ENSP00000490325.1:n.*551T>A
ENST00000636754.1:c.*607T>A	ENSP00000489781.1:n.*607T>A
ENST00000636946.1:c.*934T>A	ENSP00000490654.1:n.*934T>A
ENST00000637037.1:c.*355T>A	ENSP00000490860.1:n.*355T>A
ENST00000637347.1:n.626T>A
ENST00000637611.1:c.*321T>A	ENSP00000489682.1:n.*321T>A
ENST00000637689.1:c.-607T>A	ENSP00000490496.1:n.-607T>A
ENST00000637925.1:c.*360T>A	ENSP00000489763.1:n.*360T>A
ENST00000638049.1:c.*523T>A	ENSP00000490597.1:n.*523T>A
ENST00000676175.1:n.2504T>A
ENST00000371413.4:c.765T>A	ENSP00000360467.3:p.Pro255=
ENST00000371418.8:c.765T>A	ENSP00000360472.4:p.Pro255=
ENST00000626307.1:n.4680T>A
ENST00000626946.1:n.435T>A
ENST00000627420.2:c.*474T>A	ENSP00000487116.1:n.*474T>A
ENST00000629035.2:c.693T>A	ENSP00000486908.1:p.Pro231=
ENST00000630047.2:c.621T>A	ENSP00000485917.1:p.Pro207=
ENST00000630487.2:c.*555T>A	ENSP00000486859.1:n.*555T>A
NM_001308275.1:c.765T>A	NP_001295204.1:p.Pro255=
NM_001308276.1:c.621T>A	NP_001295205.1:p.Pro207=
NM_005097.2:c.765T>A	NP_005088.1:p.Pro255=
NM_005097.3:c.765T>A	NP_005088.1:p.Pro255=
NR_131777.1:n.1029T>A
XM_017016911.2:c.765T>A	XP_016872400.1:p.Pro255=
XM_017016912.2:c.621T>A	XP_016872401.1:p.Pro207=
NM_005097.4:c.765T>A MANE Select	NP_005088.1:p.Pro255=
NM_001308275.2:c.765T>A	NP_001295204.1:p.Pro255=
NM_001308276.2:c.621T>A	NP_001295205.1:p.Pro207=
NR_131777.2:n.902T>A