Canonical Allele Identifier: CA377624458

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553071G>T (hg19) ; chr10:g.93793314G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793314G>T , CM000672.2:g.93793314G>T	GRCh38
NC_000010.10:g.95553071G>T , CM000672.1:g.95553071G>T	GRCh37
NC_000010.9:g.95543061G>T	NCBI36
NG_011832.1:g.40506G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.802G>T MANE Select	ENSP00000360472.4:p.Val268Leu
ENST00000485458.3:n.4778G>T
ENST00000635953.1:c.802G>T	ENSP00000490058.1:p.Val268Leu
ENST00000636155.1:c.802G>T	ENSP00000490355.1:p.Val268Leu
ENST00000636232.1:c.*588G>T	ENSP00000490325.1:n.*588G>T
ENST00000636754.1:c.*644G>T	ENSP00000489781.1:n.*644G>T
ENST00000636946.1:c.*971G>T	ENSP00000490654.1:n.*971G>T
ENST00000637037.1:c.*392G>T	ENSP00000490860.1:n.*392G>T
ENST00000637347.1:n.663G>T
ENST00000637611.1:c.*358G>T	ENSP00000489682.1:n.*358G>T
ENST00000637689.1:c.-570G>T	ENSP00000490496.1:n.-570G>T
ENST00000637925.1:c.*397G>T	ENSP00000489763.1:n.*397G>T
ENST00000638049.1:c.*560G>T	ENSP00000490597.1:n.*560G>T
ENST00000676175.1:n.2541G>T
ENST00000371413.4:c.802G>T	ENSP00000360467.3:p.Val268Leu
ENST00000371418.8:c.802G>T	ENSP00000360472.4:p.Val268Leu
ENST00000626307.1:n.4717G>T
ENST00000626946.1:n.472G>T
ENST00000627420.2:c.*511G>T	ENSP00000487116.1:n.*511G>T
ENST00000629035.2:c.730G>T	ENSP00000486908.1:p.Val244Leu
ENST00000630047.2:c.658G>T	ENSP00000485917.1:p.Val220Leu
ENST00000630487.2:c.*592G>T	ENSP00000486859.1:n.*592G>T
NM_001308275.1:c.802G>T	NP_001295204.1:p.Val268Leu
NM_001308276.1:c.658G>T	NP_001295205.1:p.Val220Leu
NM_005097.2:c.802G>T	NP_005088.1:p.Val268Leu
NM_005097.3:c.802G>T	NP_005088.1:p.Val268Leu
NR_131777.1:n.1066G>T
XM_017016911.2:c.802G>T	XP_016872400.1:p.Val268Leu
XM_017016912.2:c.658G>T	XP_016872401.1:p.Val220Leu
NM_005097.4:c.802G>T MANE Select	NP_005088.1:p.Val268Leu
NM_001308275.2:c.802G>T	NP_001295204.1:p.Val268Leu
NM_001308276.2:c.658G>T	NP_001295205.1:p.Val220Leu
NR_131777.2:n.939G>T