Canonical Allele Identifier: CA377624090

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552990A>T (hg19) ; chr10:g.93793233A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793233A>T , CM000672.2:g.93793233A>T	GRCh38
NC_000010.10:g.95552990A>T , CM000672.1:g.95552990A>T	GRCh37
NC_000010.9:g.95542980A>T	NCBI36
NG_011832.1:g.40425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.721A>T MANE Select	ENSP00000360472.4:p.Thr241Ser
ENST00000485458.3:n.4697A>T
ENST00000635953.1:c.721A>T	ENSP00000490058.1:p.Thr241Ser
ENST00000636155.1:c.721A>T	ENSP00000490355.1:p.Thr241Ser
ENST00000636232.1:c.*507A>T	ENSP00000490325.1:n.*507A>T
ENST00000636754.1:c.*563A>T	ENSP00000489781.1:n.*563A>T
ENST00000636946.1:c.*890A>T	ENSP00000490654.1:n.*890A>T
ENST00000637037.1:c.*311A>T	ENSP00000490860.1:n.*311A>T
ENST00000637347.1:n.582A>T
ENST00000637611.1:c.*277A>T	ENSP00000489682.1:n.*277A>T
ENST00000637689.1:c.-651A>T	ENSP00000490496.1:n.-651A>T
ENST00000637925.1:c.*316A>T	ENSP00000489763.1:n.*316A>T
ENST00000638049.1:c.*479A>T	ENSP00000490597.1:n.*479A>T
ENST00000676175.1:n.2460A>T
ENST00000371413.4:c.721A>T	ENSP00000360467.3:p.Thr241Ser
ENST00000371418.8:c.721A>T	ENSP00000360472.4:p.Thr241Ser
ENST00000626307.1:n.4636A>T
ENST00000626946.1:n.391A>T
ENST00000627420.2:c.*430A>T	ENSP00000487116.1:n.*430A>T
ENST00000629035.2:c.649A>T	ENSP00000486908.1:p.Thr217Ser
ENST00000630047.2:c.577A>T	ENSP00000485917.1:p.Thr193Ser
ENST00000630412.1:n.509A>T
ENST00000630487.2:c.*511A>T	ENSP00000486859.1:n.*511A>T
NM_001308275.1:c.721A>T	NP_001295204.1:p.Thr241Ser
NM_001308276.1:c.577A>T	NP_001295205.1:p.Thr193Ser
NM_005097.2:c.721A>T	NP_005088.1:p.Thr241Ser
NM_005097.3:c.721A>T	NP_005088.1:p.Thr241Ser
NR_131777.1:n.985A>T
XM_017016911.2:c.721A>T	XP_016872400.1:p.Thr241Ser
XM_017016912.2:c.577A>T	XP_016872401.1:p.Thr193Ser
NM_005097.4:c.721A>T MANE Select	NP_005088.1:p.Thr241Ser
NM_001308275.2:c.721A>T	NP_001295204.1:p.Thr241Ser
NM_001308276.2:c.577A>T	NP_001295205.1:p.Thr193Ser
NR_131777.2:n.858A>T