Canonical Allele Identifier: CA377623962

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552964T>A (hg19) ; chr10:g.93793207T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793207T>A , CM000672.2:g.93793207T>A	GRCh38
NC_000010.10:g.95552964T>A , CM000672.1:g.95552964T>A	GRCh37
NC_000010.9:g.95542954T>A	NCBI36
NG_011832.1:g.40399T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.695T>A MANE Select	ENSP00000360472.4:p.Leu232Gln
ENST00000485458.3:n.4671T>A
ENST00000635953.1:c.695T>A	ENSP00000490058.1:p.Leu232Gln
ENST00000636155.1:c.695T>A	ENSP00000490355.1:p.Leu232Gln
ENST00000636232.1:c.*481T>A	ENSP00000490325.1:n.*481T>A
ENST00000636754.1:c.*537T>A	ENSP00000489781.1:n.*537T>A
ENST00000636946.1:c.*864T>A	ENSP00000490654.1:n.*864T>A
ENST00000637037.1:c.*285T>A	ENSP00000490860.1:n.*285T>A
ENST00000637347.1:n.556T>A
ENST00000637611.1:c.*251T>A	ENSP00000489682.1:n.*251T>A
ENST00000637689.1:c.-677T>A	ENSP00000490496.1:n.-677T>A
ENST00000637925.1:c.*290T>A	ENSP00000489763.1:n.*290T>A
ENST00000638049.1:c.*453T>A	ENSP00000490597.1:n.*453T>A
ENST00000676175.1:n.2434T>A
ENST00000371413.4:c.695T>A	ENSP00000360467.3:p.Leu232Gln
ENST00000371418.8:c.695T>A	ENSP00000360472.4:p.Leu232Gln
ENST00000626307.1:n.4610T>A
ENST00000626946.1:n.365T>A
ENST00000627420.2:c.*404T>A	ENSP00000487116.1:n.*404T>A
ENST00000629035.2:c.623T>A	ENSP00000486908.1:p.Leu208Gln
ENST00000630047.2:c.551T>A	ENSP00000485917.1:p.Leu184Gln
ENST00000630412.1:n.483T>A
ENST00000630487.2:c.*485T>A	ENSP00000486859.1:n.*485T>A
NM_001308275.1:c.695T>A	NP_001295204.1:p.Leu232Gln
NM_001308276.1:c.551T>A	NP_001295205.1:p.Leu184Gln
NM_005097.2:c.695T>A	NP_005088.1:p.Leu232Gln
NM_005097.3:c.695T>A	NP_005088.1:p.Leu232Gln
NR_131777.1:n.959T>A
XM_017016911.2:c.695T>A	XP_016872400.1:p.Leu232Gln
XM_017016912.2:c.551T>A	XP_016872401.1:p.Leu184Gln
NM_005097.4:c.695T>A MANE Select	NP_005088.1:p.Leu232Gln
NM_001308275.2:c.695T>A	NP_001295204.1:p.Leu232Gln
NM_001308276.2:c.551T>A	NP_001295205.1:p.Leu184Gln
NR_131777.2:n.832T>A