Canonical Allele Identifier: CA377624158

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553010T>A (hg19) ; chr10:g.93793253T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793253T>A , CM000672.2:g.93793253T>A	GRCh38
NC_000010.10:g.95553010T>A , CM000672.1:g.95553010T>A	GRCh37
NC_000010.9:g.95543000T>A	NCBI36
NG_011832.1:g.40445T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.741T>A MANE Select	ENSP00000360472.4:p.Asp247Glu
ENST00000485458.3:n.4717T>A
ENST00000635953.1:c.741T>A	ENSP00000490058.1:p.Asp247Glu
ENST00000636155.1:c.741T>A	ENSP00000490355.1:p.Asp247Glu
ENST00000636232.1:c.*527T>A	ENSP00000490325.1:n.*527T>A
ENST00000636754.1:c.*583T>A	ENSP00000489781.1:n.*583T>A
ENST00000636946.1:c.*910T>A	ENSP00000490654.1:n.*910T>A
ENST00000637037.1:c.*331T>A	ENSP00000490860.1:n.*331T>A
ENST00000637347.1:n.602T>A
ENST00000637611.1:c.*297T>A	ENSP00000489682.1:n.*297T>A
ENST00000637689.1:c.-631T>A	ENSP00000490496.1:n.-631T>A
ENST00000637925.1:c.*336T>A	ENSP00000489763.1:n.*336T>A
ENST00000638049.1:c.*499T>A	ENSP00000490597.1:n.*499T>A
ENST00000676175.1:n.2480T>A
ENST00000371413.4:c.741T>A	ENSP00000360467.3:p.Asp247Glu
ENST00000371418.8:c.741T>A	ENSP00000360472.4:p.Asp247Glu
ENST00000626307.1:n.4656T>A
ENST00000626946.1:n.411T>A
ENST00000627420.2:c.*450T>A	ENSP00000487116.1:n.*450T>A
ENST00000629035.2:c.669T>A	ENSP00000486908.1:p.Asp223Glu
ENST00000630047.2:c.597T>A	ENSP00000485917.1:p.Asp199Glu
ENST00000630412.1:n.529T>A
ENST00000630487.2:c.*531T>A	ENSP00000486859.1:n.*531T>A
NM_001308275.1:c.741T>A	NP_001295204.1:p.Asp247Glu
NM_001308276.1:c.597T>A	NP_001295205.1:p.Asp199Glu
NM_005097.2:c.741T>A	NP_005088.1:p.Asp247Glu
NM_005097.3:c.741T>A	NP_005088.1:p.Asp247Glu
NR_131777.1:n.1005T>A
XM_017016911.2:c.741T>A	XP_016872400.1:p.Asp247Glu
XM_017016912.2:c.597T>A	XP_016872401.1:p.Asp199Glu
NM_005097.4:c.741T>A MANE Select	NP_005088.1:p.Asp247Glu
NM_001308275.2:c.741T>A	NP_001295204.1:p.Asp247Glu
NM_001308276.2:c.597T>A	NP_001295205.1:p.Asp199Glu
NR_131777.2:n.878T>A