Canonical Allele Identifier: CA377623998

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552973A>G (hg19) ; chr10:g.93793216A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793216A>G , CM000672.2:g.93793216A>G	GRCh38
NC_000010.10:g.95552973A>G , CM000672.1:g.95552973A>G	GRCh37
NC_000010.9:g.95542963A>G	NCBI36
NG_011832.1:g.40408A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.704A>G MANE Select	ENSP00000360472.4:p.Gln235Arg
ENST00000485458.3:n.4680A>G
ENST00000635953.1:c.704A>G	ENSP00000490058.1:p.Gln235Arg
ENST00000636155.1:c.704A>G	ENSP00000490355.1:p.Gln235Arg
ENST00000636232.1:c.*490A>G	ENSP00000490325.1:n.*490A>G
ENST00000636754.1:c.*546A>G	ENSP00000489781.1:n.*546A>G
ENST00000636946.1:c.*873A>G	ENSP00000490654.1:n.*873A>G
ENST00000637037.1:c.*294A>G	ENSP00000490860.1:n.*294A>G
ENST00000637347.1:n.565A>G
ENST00000637611.1:c.*260A>G	ENSP00000489682.1:n.*260A>G
ENST00000637689.1:c.-668A>G	ENSP00000490496.1:n.-668A>G
ENST00000637925.1:c.*299A>G	ENSP00000489763.1:n.*299A>G
ENST00000638049.1:c.*462A>G	ENSP00000490597.1:n.*462A>G
ENST00000676175.1:n.2443A>G
ENST00000371413.4:c.704A>G	ENSP00000360467.3:p.Gln235Arg
ENST00000371418.8:c.704A>G	ENSP00000360472.4:p.Gln235Arg
ENST00000626307.1:n.4619A>G
ENST00000626946.1:n.374A>G
ENST00000627420.2:c.*413A>G	ENSP00000487116.1:n.*413A>G
ENST00000629035.2:c.632A>G	ENSP00000486908.1:p.Gln211Arg
ENST00000630047.2:c.560A>G	ENSP00000485917.1:p.Gln187Arg
ENST00000630412.1:n.492A>G
ENST00000630487.2:c.*494A>G	ENSP00000486859.1:n.*494A>G
NM_001308275.1:c.704A>G	NP_001295204.1:p.Gln235Arg
NM_001308276.1:c.560A>G	NP_001295205.1:p.Gln187Arg
NM_005097.2:c.704A>G	NP_005088.1:p.Gln235Arg
NM_005097.3:c.704A>G	NP_005088.1:p.Gln235Arg
NR_131777.1:n.968A>G
XM_017016911.2:c.704A>G	XP_016872400.1:p.Gln235Arg
XM_017016912.2:c.560A>G	XP_016872401.1:p.Gln187Arg
NM_005097.4:c.704A>G MANE Select	NP_005088.1:p.Gln235Arg
NM_001308275.2:c.704A>G	NP_001295204.1:p.Gln235Arg
NM_001308276.2:c.560A>G	NP_001295205.1:p.Gln187Arg
NR_131777.2:n.841A>G