Canonical Allele Identifier: CA470985300

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557056A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797299A>T , CM000672.2:g.93797299A>T	GRCh38
NC_000010.10:g.95557056A>T , CM000672.1:g.95557056A>T	GRCh37
NC_000010.9:g.95547046A>T	NCBI36
NG_011832.1:g.44491A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.1170A>T MANE Select	ENSP00000360472.4:p.Thr390=
ENST00000485458.3:n.5146A>T
ENST00000635804.1:n.604A>T
ENST00000635953.1:c.*592A>T	ENSP00000490058.1:n.*592A>T
ENST00000636155.1:c.838+3949A>T	ENSP00000490355.1:n.838+3949A>T
ENST00000636232.1:c.*956A>T	ENSP00000490325.1:n.*956A>T
ENST00000636754.1:c.*1012A>T	ENSP00000489781.1:n.*1012A>T
ENST00000636946.1:c.*1008-450A>T	ENSP00000490654.1:n.*1008-450A>T
ENST00000637037.1:c.*760A>T	ENSP00000490860.1:n.*760A>T
ENST00000637347.1:n.1031A>T
ENST00000637611.1:c.*726A>T	ENSP00000489682.1:n.*726A>T
ENST00000637689.1:c.-202A>T	ENSP00000490496.1:n.-202A>T
ENST00000637925.1:c.*765A>T	ENSP00000489763.1:n.*765A>T
ENST00000638049.1:c.*928A>T	ENSP00000490597.1:n.*928A>T
ENST00000676175.1:n.2909A>T
ENST00000371413.4:c.839-450A>T	ENSP00000360467.3:n.839-450A>T
ENST00000371418.8:c.1170A>T	ENSP00000360472.4:p.Thr390=
ENST00000626307.1:n.5085A>T
ENST00000627420.2:c.*879A>T	ENSP00000487116.1:n.*879A>T
ENST00000629035.2:c.1098A>T	ENSP00000486908.1:p.Thr366=
ENST00000630047.2:c.1026A>T	ENSP00000485917.1:p.Thr342=
NM_001308275.1:c.839-450A>T	NP_001295204.1:n.839-450A>T
NM_001308276.1:c.1026A>T	NP_001295205.1:p.Thr342=
NM_005097.2:c.1170A>T	NP_005088.1:p.Thr390=
NM_005097.3:c.1170A>T	NP_005088.1:p.Thr390=
NR_131777.1:n.1434A>T
XM_017016912.2:c.695-450A>T	XP_016872401.1:n.695-450A>T
NM_005097.4:c.1170A>T MANE Select	NP_005088.1:p.Thr390=
NM_001308275.2:c.839-450A>T	NP_001295204.1:n.839-450A>T
NM_001308276.2:c.1026A>T	NP_001295205.1:p.Thr342=
NR_131777.2:n.1307A>T