Canonical Allele Identifier: CA470800723

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556840C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797083C>T , CM000672.2:g.93797083C>T	GRCh38
NC_000010.10:g.95556840C>T , CM000672.1:g.95556840C>T	GRCh37
NC_000010.9:g.95546830C>T	NCBI36
NG_011832.1:g.44275C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.954C>T MANE Select	ENSP00000360472.4:p.Phe318=
ENST00000485458.3:n.4930C>T
ENST00000635804.1:n.388C>T
ENST00000635953.1:c.*376C>T	ENSP00000490058.1:n.*376C>T
ENST00000636155.1:c.838+3733C>T	ENSP00000490355.1:n.838+3733C>T
ENST00000636232.1:c.*740C>T	ENSP00000490325.1:n.*740C>T
ENST00000636754.1:c.*796C>T	ENSP00000489781.1:n.*796C>T
ENST00000636946.1:c.*1008-666C>T	ENSP00000490654.1:n.*1008-666C>T
ENST00000637037.1:c.*544C>T	ENSP00000490860.1:n.*544C>T
ENST00000637347.1:n.815C>T
ENST00000637611.1:c.*510C>T	ENSP00000489682.1:n.*510C>T
ENST00000637689.1:c.-418C>T	ENSP00000490496.1:n.-418C>T
ENST00000637925.1:c.*549C>T	ENSP00000489763.1:n.*549C>T
ENST00000638049.1:c.*712C>T	ENSP00000490597.1:n.*712C>T
ENST00000676175.1:n.2693C>T
ENST00000371413.4:c.839-666C>T	ENSP00000360467.3:n.839-666C>T
ENST00000371418.8:c.954C>T	ENSP00000360472.4:p.Phe318=
ENST00000626307.1:n.4869C>T
ENST00000627420.2:c.*663C>T	ENSP00000487116.1:n.*663C>T
ENST00000629035.2:c.882C>T	ENSP00000486908.1:p.Phe294=
ENST00000630047.2:c.810C>T	ENSP00000485917.1:p.Phe270=
NM_001308275.1:c.839-666C>T	NP_001295204.1:n.839-666C>T
NM_001308276.1:c.810C>T	NP_001295205.1:p.Phe270=
NM_005097.2:c.954C>T	NP_005088.1:p.Phe318=
NM_005097.3:c.954C>T	NP_005088.1:p.Phe318=
NR_131777.1:n.1218C>T
XM_017016912.2:c.695-666C>T	XP_016872401.1:n.695-666C>T
NM_005097.4:c.954C>T MANE Select	NP_005088.1:p.Phe318=
NM_001308275.2:c.839-666C>T	NP_001295204.1:n.839-666C>T
NM_001308276.2:c.810C>T	NP_001295205.1:p.Phe270=
NR_131777.2:n.1091C>T