Canonical Allele Identifier: CA470800133

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553058T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793301T>G , CM000672.2:g.93793301T>G	GRCh38
NC_000010.10:g.95553058T>G , CM000672.1:g.95553058T>G	GRCh37
NC_000010.9:g.95543048T>G	NCBI36
NG_011832.1:g.40493T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.789T>G MANE Select	ENSP00000360472.4:p.Leu263=
ENST00000485458.3:n.4765T>G
ENST00000635953.1:c.789T>G	ENSP00000490058.1:p.Leu263=
ENST00000636155.1:c.789T>G	ENSP00000490355.1:p.Leu263=
ENST00000636232.1:c.*575T>G	ENSP00000490325.1:n.*575T>G
ENST00000636754.1:c.*631T>G	ENSP00000489781.1:n.*631T>G
ENST00000636946.1:c.*958T>G	ENSP00000490654.1:n.*958T>G
ENST00000637037.1:c.*379T>G	ENSP00000490860.1:n.*379T>G
ENST00000637347.1:n.650T>G
ENST00000637611.1:c.*345T>G	ENSP00000489682.1:n.*345T>G
ENST00000637689.1:c.-583T>G	ENSP00000490496.1:n.-583T>G
ENST00000637925.1:c.*384T>G	ENSP00000489763.1:n.*384T>G
ENST00000638049.1:c.*547T>G	ENSP00000490597.1:n.*547T>G
ENST00000676175.1:n.2528T>G
ENST00000371413.4:c.789T>G	ENSP00000360467.3:p.Leu263=
ENST00000371418.8:c.789T>G	ENSP00000360472.4:p.Leu263=
ENST00000626307.1:n.4704T>G
ENST00000626946.1:n.459T>G
ENST00000627420.2:c.*498T>G	ENSP00000487116.1:n.*498T>G
ENST00000629035.2:c.717T>G	ENSP00000486908.1:p.Leu239=
ENST00000630047.2:c.645T>G	ENSP00000485917.1:p.Leu215=
ENST00000630487.2:c.*579T>G	ENSP00000486859.1:n.*579T>G
NM_001308275.1:c.789T>G	NP_001295204.1:p.Leu263=
NM_001308276.1:c.645T>G	NP_001295205.1:p.Leu215=
NM_005097.2:c.789T>G	NP_005088.1:p.Leu263=
NM_005097.3:c.789T>G	NP_005088.1:p.Leu263=
NR_131777.1:n.1053T>G
XM_017016911.2:c.789T>G	XP_016872400.1:p.Leu263=
XM_017016912.2:c.645T>G	XP_016872401.1:p.Leu215=
NM_005097.4:c.789T>G MANE Select	NP_005088.1:p.Leu263=
NM_001308275.2:c.789T>G	NP_001295204.1:p.Leu263=
NM_001308276.2:c.645T>G	NP_001295205.1:p.Leu215=
NR_131777.2:n.926T>G