Canonical Allele Identifier: CA377627854

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557017C>A (hg19) ; chr10:g.93797260C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797260C>A , CM000672.2:g.93797260C>A	GRCh38
NC_000010.10:g.95557017C>A , CM000672.1:g.95557017C>A	GRCh37
NC_000010.9:g.95547007C>A	NCBI36
NG_011832.1:g.44452C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1131C>A MANE Select	ENSP00000360472.4:p.Tyr377Ter
ENST00000485458.3:n.5107C>A
ENST00000635804.1:n.565C>A
ENST00000635953.1:c.*553C>A	ENSP00000490058.1:n.*553C>A
ENST00000636155.1:c.838+3910C>A	ENSP00000490355.1:n.838+3910C>A
ENST00000636232.1:c.*917C>A	ENSP00000490325.1:n.*917C>A
ENST00000636754.1:c.*973C>A	ENSP00000489781.1:n.*973C>A
ENST00000636946.1:c.*1008-489C>A	ENSP00000490654.1:n.*1008-489C>A
ENST00000637037.1:c.*721C>A	ENSP00000490860.1:n.*721C>A
ENST00000637347.1:n.992C>A
ENST00000637611.1:c.*687C>A	ENSP00000489682.1:n.*687C>A
ENST00000637689.1:c.-241C>A	ENSP00000490496.1:n.-241C>A
ENST00000637925.1:c.*726C>A	ENSP00000489763.1:n.*726C>A
ENST00000638049.1:c.*889C>A	ENSP00000490597.1:n.*889C>A
ENST00000676175.1:n.2870C>A
ENST00000371413.4:c.839-489C>A	ENSP00000360467.3:n.839-489C>A
ENST00000371418.8:c.1131C>A	ENSP00000360472.4:p.Tyr377Ter
ENST00000626307.1:n.5046C>A
ENST00000627420.2:c.*840C>A	ENSP00000487116.1:n.*840C>A
ENST00000629035.2:c.1059C>A	ENSP00000486908.1:p.Tyr353Ter
ENST00000630047.2:c.987C>A	ENSP00000485917.1:p.Tyr329Ter
NM_001308275.1:c.839-489C>A	NP_001295204.1:n.839-489C>A
NM_001308276.1:c.987C>A	NP_001295205.1:p.Tyr329Ter
NM_005097.2:c.1131C>A	NP_005088.1:p.Tyr377Ter
NM_005097.3:c.1131C>A	NP_005088.1:p.Tyr377Ter
NR_131777.1:n.1395C>A
XM_017016912.2:c.695-489C>A	XP_016872401.1:n.695-489C>A
NM_005097.4:c.1131C>A MANE Select	NP_005088.1:p.Tyr377Ter
NM_001308275.2:c.839-489C>A	NP_001295204.1:n.839-489C>A
NM_001308276.2:c.987C>A	NP_001295205.1:p.Tyr329Ter
NR_131777.2:n.1268C>A