Canonical Allele Identifier: CA377627988

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557040T>A (hg19) ; chr10:g.93797283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797283T>A , CM000672.2:g.93797283T>A	GRCh38
NC_000010.10:g.95557040T>A , CM000672.1:g.95557040T>A	GRCh37
NC_000010.9:g.95547030T>A	NCBI36
NG_011832.1:g.44475T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1154T>A MANE Select	ENSP00000360472.4:p.Leu385Gln
ENST00000485458.3:n.5130T>A
ENST00000635804.1:n.588T>A
ENST00000635953.1:c.*576T>A	ENSP00000490058.1:n.*576T>A
ENST00000636155.1:c.838+3933T>A	ENSP00000490355.1:n.838+3933T>A
ENST00000636232.1:c.*940T>A	ENSP00000490325.1:n.*940T>A
ENST00000636754.1:c.*996T>A	ENSP00000489781.1:n.*996T>A
ENST00000636946.1:c.*1008-466T>A	ENSP00000490654.1:n.*1008-466T>A
ENST00000637037.1:c.*744T>A	ENSP00000490860.1:n.*744T>A
ENST00000637347.1:n.1015T>A
ENST00000637611.1:c.*710T>A	ENSP00000489682.1:n.*710T>A
ENST00000637689.1:c.-218T>A	ENSP00000490496.1:n.-218T>A
ENST00000637925.1:c.*749T>A	ENSP00000489763.1:n.*749T>A
ENST00000638049.1:c.*912T>A	ENSP00000490597.1:n.*912T>A
ENST00000676175.1:n.2893T>A
ENST00000371413.4:c.839-466T>A	ENSP00000360467.3:n.839-466T>A
ENST00000371418.8:c.1154T>A	ENSP00000360472.4:p.Leu385Gln
ENST00000626307.1:n.5069T>A
ENST00000627420.2:c.*863T>A	ENSP00000487116.1:n.*863T>A
ENST00000629035.2:c.1082T>A	ENSP00000486908.1:p.Leu361Gln
ENST00000630047.2:c.1010T>A	ENSP00000485917.1:p.Leu337Gln
NM_001308275.1:c.839-466T>A	NP_001295204.1:n.839-466T>A
NM_001308276.1:c.1010T>A	NP_001295205.1:p.Leu337Gln
NM_005097.2:c.1154T>A	NP_005088.1:p.Leu385Gln
NM_005097.3:c.1154T>A	NP_005088.1:p.Leu385Gln
NR_131777.1:n.1418T>A
XM_017016912.2:c.695-466T>A	XP_016872401.1:n.695-466T>A
NM_005097.4:c.1154T>A MANE Select	NP_005088.1:p.Leu385Gln
NM_001308275.2:c.839-466T>A	NP_001295204.1:n.839-466T>A
NM_001308276.2:c.1010T>A	NP_001295205.1:p.Leu337Gln
NR_131777.2:n.1291T>A