Canonical Allele Identifier: CA377623885

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552945T>G (hg19) ; chr10:g.93793188T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793188T>G , CM000672.2:g.93793188T>G	GRCh38
NC_000010.10:g.95552945T>G , CM000672.1:g.95552945T>G	GRCh37
NC_000010.9:g.95542935T>G	NCBI36
NG_011832.1:g.40380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.676T>G MANE Select	ENSP00000360472.4:p.Phe226Val
ENST00000485458.3:n.4652T>G
ENST00000635953.1:c.676T>G	ENSP00000490058.1:p.Phe226Val
ENST00000636155.1:c.676T>G	ENSP00000490355.1:p.Phe226Val
ENST00000636232.1:c.*462T>G	ENSP00000490325.1:n.*462T>G
ENST00000636754.1:c.*518T>G	ENSP00000489781.1:n.*518T>G
ENST00000636946.1:c.*845T>G	ENSP00000490654.1:n.*845T>G
ENST00000637037.1:c.*266T>G	ENSP00000490860.1:n.*266T>G
ENST00000637347.1:n.537T>G
ENST00000637611.1:c.*232T>G	ENSP00000489682.1:n.*232T>G
ENST00000637689.1:c.-696T>G	ENSP00000490496.1:n.-696T>G
ENST00000637925.1:c.*271T>G	ENSP00000489763.1:n.*271T>G
ENST00000638049.1:c.*434T>G	ENSP00000490597.1:n.*434T>G
ENST00000676175.1:n.2415T>G
ENST00000371413.4:c.676T>G	ENSP00000360467.3:p.Phe226Val
ENST00000371418.8:c.676T>G	ENSP00000360472.4:p.Phe226Val
ENST00000626307.1:n.4591T>G
ENST00000626946.1:n.346T>G
ENST00000627420.2:c.*385T>G	ENSP00000487116.1:n.*385T>G
ENST00000629035.2:c.604T>G	ENSP00000486908.1:p.Phe202Val
ENST00000630047.2:c.532T>G	ENSP00000485917.1:p.Phe178Val
ENST00000630412.1:n.464T>G
ENST00000630487.2:c.*466T>G	ENSP00000486859.1:n.*466T>G
NM_001308275.1:c.676T>G	NP_001295204.1:p.Phe226Val
NM_001308276.1:c.532T>G	NP_001295205.1:p.Phe178Val
NM_005097.2:c.676T>G	NP_005088.1:p.Phe226Val
NM_005097.3:c.676T>G	NP_005088.1:p.Phe226Val
NR_131777.1:n.940T>G
XM_017016911.2:c.676T>G	XP_016872400.1:p.Phe226Val
XM_017016912.2:c.532T>G	XP_016872401.1:p.Phe178Val
NM_005097.4:c.676T>G MANE Select	NP_005088.1:p.Phe226Val
NM_001308275.2:c.676T>G	NP_001295204.1:p.Phe226Val
NM_001308276.2:c.532T>G	NP_001295205.1:p.Phe178Val
NR_131777.2:n.813T>G