Canonical Allele Identifier: CA377626660

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556839T>A (hg19) ; chr10:g.93797082T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797082T>A , CM000672.2:g.93797082T>A	GRCh38
NC_000010.10:g.95556839T>A , CM000672.1:g.95556839T>A	GRCh37
NC_000010.9:g.95546829T>A	NCBI36
NG_011832.1:g.44274T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.953T>A MANE Select	ENSP00000360472.4:p.Phe318Tyr
ENST00000485458.3:n.4929T>A
ENST00000635804.1:n.387T>A
ENST00000635953.1:c.*375T>A	ENSP00000490058.1:n.*375T>A
ENST00000636155.1:c.838+3732T>A	ENSP00000490355.1:n.838+3732T>A
ENST00000636232.1:c.*739T>A	ENSP00000490325.1:n.*739T>A
ENST00000636754.1:c.*795T>A	ENSP00000489781.1:n.*795T>A
ENST00000636946.1:c.*1008-667T>A	ENSP00000490654.1:n.*1008-667T>A
ENST00000637037.1:c.*543T>A	ENSP00000490860.1:n.*543T>A
ENST00000637347.1:n.814T>A
ENST00000637611.1:c.*509T>A	ENSP00000489682.1:n.*509T>A
ENST00000637689.1:c.-419T>A	ENSP00000490496.1:n.-419T>A
ENST00000637925.1:c.*548T>A	ENSP00000489763.1:n.*548T>A
ENST00000638049.1:c.*711T>A	ENSP00000490597.1:n.*711T>A
ENST00000676175.1:n.2692T>A
ENST00000371413.4:c.839-667T>A	ENSP00000360467.3:n.839-667T>A
ENST00000371418.8:c.953T>A	ENSP00000360472.4:p.Phe318Tyr
ENST00000626307.1:n.4868T>A
ENST00000627420.2:c.*662T>A	ENSP00000487116.1:n.*662T>A
ENST00000629035.2:c.881T>A	ENSP00000486908.1:p.Phe294Tyr
ENST00000630047.2:c.809T>A	ENSP00000485917.1:p.Phe270Tyr
NM_001308275.1:c.839-667T>A	NP_001295204.1:n.839-667T>A
NM_001308276.1:c.809T>A	NP_001295205.1:p.Phe270Tyr
NM_005097.2:c.953T>A	NP_005088.1:p.Phe318Tyr
NM_005097.3:c.953T>A	NP_005088.1:p.Phe318Tyr
NR_131777.1:n.1217T>A
XM_017016912.2:c.695-667T>A	XP_016872401.1:n.695-667T>A
NM_005097.4:c.953T>A MANE Select	NP_005088.1:p.Phe318Tyr
NM_001308275.2:c.839-667T>A	NP_001295204.1:n.839-667T>A
NM_001308276.2:c.809T>A	NP_001295205.1:p.Phe270Tyr
NR_131777.2:n.1090T>A