Canonical Allele Identifier: CA377628152

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557071A>T (hg19) ; chr10:g.93797314A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797314A>T , CM000672.2:g.93797314A>T	GRCh38
NC_000010.10:g.95557071A>T , CM000672.1:g.95557071A>T	GRCh37
NC_000010.9:g.95547061A>T	NCBI36
NG_011832.1:g.44506A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1185A>T MANE Select	ENSP00000360472.4:p.Arg395Ser
ENST00000485458.3:n.5161A>T
ENST00000635804.1:n.619A>T
ENST00000635953.1:c.*607A>T	ENSP00000490058.1:n.*607A>T
ENST00000636155.1:c.838+3964A>T	ENSP00000490355.1:n.838+3964A>T
ENST00000636232.1:c.*971A>T	ENSP00000490325.1:n.*971A>T
ENST00000636754.1:c.*1027A>T	ENSP00000489781.1:n.*1027A>T
ENST00000636946.1:c.*1008-435A>T	ENSP00000490654.1:n.*1008-435A>T
ENST00000637037.1:c.*775A>T	ENSP00000490860.1:n.*775A>T
ENST00000637347.1:n.1046A>T
ENST00000637611.1:c.*741A>T	ENSP00000489682.1:n.*741A>T
ENST00000637689.1:c.-187A>T	ENSP00000490496.1:n.-187A>T
ENST00000637925.1:c.*780A>T	ENSP00000489763.1:n.*780A>T
ENST00000638049.1:c.*943A>T	ENSP00000490597.1:n.*943A>T
ENST00000676175.1:n.2924A>T
ENST00000371413.4:c.839-435A>T	ENSP00000360467.3:n.839-435A>T
ENST00000371418.8:c.1185A>T	ENSP00000360472.4:p.Arg395Ser
ENST00000626307.1:n.5100A>T
ENST00000627420.2:c.*894A>T	ENSP00000487116.1:n.*894A>T
ENST00000629035.2:c.1113A>T	ENSP00000486908.1:p.Arg371Ser
ENST00000630047.2:c.1041A>T	ENSP00000485917.1:p.Arg347Ser
NM_001308275.1:c.839-435A>T	NP_001295204.1:n.839-435A>T
NM_001308276.1:c.1041A>T	NP_001295205.1:p.Arg347Ser
NM_005097.2:c.1185A>T	NP_005088.1:p.Arg395Ser
NM_005097.3:c.1185A>T	NP_005088.1:p.Arg395Ser
NR_131777.1:n.1449A>T
XM_017016912.2:c.695-435A>T	XP_016872401.1:n.695-435A>T
NM_005097.4:c.1185A>T MANE Select	NP_005088.1:p.Arg395Ser
NM_001308275.2:c.839-435A>T	NP_001295204.1:n.839-435A>T
NM_001308276.2:c.1041A>T	NP_001295205.1:p.Arg347Ser
NR_131777.2:n.1322A>T