Canonical Allele Identifier: CA377627236

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556925G>T (hg19) ; chr10:g.93797168G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797168G>T , CM000672.2:g.93797168G>T	GRCh38
NC_000010.10:g.95556925G>T , CM000672.1:g.95556925G>T	GRCh37
NC_000010.9:g.95546915G>T	NCBI36
NG_011832.1:g.44360G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1039G>T MANE Select	ENSP00000360472.4:p.Val347Phe
ENST00000485458.3:n.5015G>T
ENST00000635804.1:n.473G>T
ENST00000635953.1:c.*461G>T	ENSP00000490058.1:n.*461G>T
ENST00000636155.1:c.838+3818G>T	ENSP00000490355.1:n.838+3818G>T
ENST00000636232.1:c.*825G>T	ENSP00000490325.1:n.*825G>T
ENST00000636754.1:c.*881G>T	ENSP00000489781.1:n.*881G>T
ENST00000636946.1:c.*1008-581G>T	ENSP00000490654.1:n.*1008-581G>T
ENST00000637037.1:c.*629G>T	ENSP00000490860.1:n.*629G>T
ENST00000637347.1:n.900G>T
ENST00000637611.1:c.*595G>T	ENSP00000489682.1:n.*595G>T
ENST00000637689.1:c.-333G>T	ENSP00000490496.1:n.-333G>T
ENST00000637925.1:c.*634G>T	ENSP00000489763.1:n.*634G>T
ENST00000638049.1:c.*797G>T	ENSP00000490597.1:n.*797G>T
ENST00000676175.1:n.2778G>T
ENST00000371413.4:c.839-581G>T	ENSP00000360467.3:n.839-581G>T
ENST00000371418.8:c.1039G>T	ENSP00000360472.4:p.Val347Phe
ENST00000626307.1:n.4954G>T
ENST00000627420.2:c.*748G>T	ENSP00000487116.1:n.*748G>T
ENST00000629035.2:c.967G>T	ENSP00000486908.1:p.Val323Phe
ENST00000630047.2:c.895G>T	ENSP00000485917.1:p.Val299Phe
NM_001308275.1:c.839-581G>T	NP_001295204.1:n.839-581G>T
NM_001308276.1:c.895G>T	NP_001295205.1:p.Val299Phe
NM_005097.2:c.1039G>T	NP_005088.1:p.Val347Phe
NM_005097.3:c.1039G>T	NP_005088.1:p.Val347Phe
NR_131777.1:n.1303G>T
XM_017016912.2:c.695-581G>T	XP_016872401.1:n.695-581G>T
NM_005097.4:c.1039G>T MANE Select	NP_005088.1:p.Val347Phe
NM_001308275.2:c.839-581G>T	NP_001295204.1:n.839-581G>T
NM_001308276.2:c.895G>T	NP_001295205.1:p.Val299Phe
NR_131777.2:n.1176G>T