Canonical Allele Identifier: CA470800395

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556741A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93796984A>G , CM000672.2:g.93796984A>G	GRCh38
NC_000010.10:g.95556741A>G , CM000672.1:g.95556741A>G	GRCh37
NC_000010.9:g.95546731A>G	NCBI36
NG_011832.1:g.44176A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.855A>G MANE Select	ENSP00000360472.4:p.Val285=
ENST00000485458.3:n.4831A>G
ENST00000635804.1:n.289A>G
ENST00000635953.1:c.*277A>G	ENSP00000490058.1:n.*277A>G
ENST00000636155.1:c.838+3634A>G	ENSP00000490355.1:n.838+3634A>G
ENST00000636232.1:c.*641A>G	ENSP00000490325.1:n.*641A>G
ENST00000636754.1:c.*697A>G	ENSP00000489781.1:n.*697A>G
ENST00000636946.1:c.*1008-765A>G	ENSP00000490654.1:n.*1008-765A>G
ENST00000637037.1:c.*445A>G	ENSP00000490860.1:n.*445A>G
ENST00000637347.1:n.716A>G
ENST00000637611.1:c.*411A>G	ENSP00000489682.1:n.*411A>G
ENST00000637689.1:c.-517A>G	ENSP00000490496.1:n.-517A>G
ENST00000637925.1:c.*450A>G	ENSP00000489763.1:n.*450A>G
ENST00000638049.1:c.*613A>G	ENSP00000490597.1:n.*613A>G
ENST00000676175.1:n.2594A>G
ENST00000371413.4:c.839-765A>G	ENSP00000360467.3:n.839-765A>G
ENST00000371418.8:c.855A>G	ENSP00000360472.4:p.Val285=
ENST00000626307.1:n.4770A>G
ENST00000626946.1:n.525A>G
ENST00000627420.2:c.*564A>G	ENSP00000487116.1:n.*564A>G
ENST00000629035.2:c.783A>G	ENSP00000486908.1:p.Val261=
ENST00000630047.2:c.711A>G	ENSP00000485917.1:p.Val237=
NM_001308275.1:c.839-765A>G	NP_001295204.1:n.839-765A>G
NM_001308276.1:c.711A>G	NP_001295205.1:p.Val237=
NM_005097.2:c.855A>G	NP_005088.1:p.Val285=
NM_005097.3:c.855A>G	NP_005088.1:p.Val285=
NR_131777.1:n.1119A>G
XM_017016912.2:c.695-765A>G	XP_016872401.1:n.695-765A>G
NM_005097.4:c.855A>G MANE Select	NP_005088.1:p.Val285=
NM_001308275.2:c.839-765A>G	NP_001295204.1:n.839-765A>G
NM_001308276.2:c.711A>G	NP_001295205.1:p.Val237=
NR_131777.2:n.992A>G