Canonical Allele Identifier: CA470985131

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556927T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797170T>C , CM000672.2:g.93797170T>C	GRCh38
NC_000010.10:g.95556927T>C , CM000672.1:g.95556927T>C	GRCh37
NC_000010.9:g.95546917T>C	NCBI36
NG_011832.1:g.44362T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1041T>C MANE Select	ENSP00000360472.4:p.Val347=
ENST00000485458.3:n.5017T>C
ENST00000635804.1:n.475T>C
ENST00000635953.1:c.*463T>C	ENSP00000490058.1:n.*463T>C
ENST00000636155.1:c.838+3820T>C	ENSP00000490355.1:n.838+3820T>C
ENST00000636232.1:c.*827T>C	ENSP00000490325.1:n.*827T>C
ENST00000636754.1:c.*883T>C	ENSP00000489781.1:n.*883T>C
ENST00000636946.1:c.*1008-579T>C	ENSP00000490654.1:n.*1008-579T>C
ENST00000637037.1:c.*631T>C	ENSP00000490860.1:n.*631T>C
ENST00000637347.1:n.902T>C
ENST00000637611.1:c.*597T>C	ENSP00000489682.1:n.*597T>C
ENST00000637689.1:c.-331T>C	ENSP00000490496.1:n.-331T>C
ENST00000637925.1:c.*636T>C	ENSP00000489763.1:n.*636T>C
ENST00000638049.1:c.*799T>C	ENSP00000490597.1:n.*799T>C
ENST00000676175.1:n.2780T>C
ENST00000371413.4:c.839-579T>C	ENSP00000360467.3:n.839-579T>C
ENST00000371418.8:c.1041T>C	ENSP00000360472.4:p.Val347=
ENST00000626307.1:n.4956T>C
ENST00000627420.2:c.*750T>C	ENSP00000487116.1:n.*750T>C
ENST00000629035.2:c.969T>C	ENSP00000486908.1:p.Val323=
ENST00000630047.2:c.897T>C	ENSP00000485917.1:p.Val299=
NM_001308275.1:c.839-579T>C	NP_001295204.1:n.839-579T>C
NM_001308276.1:c.897T>C	NP_001295205.1:p.Val299=
NM_005097.2:c.1041T>C	NP_005088.1:p.Val347=
NM_005097.3:c.1041T>C	NP_005088.1:p.Val347=
NR_131777.1:n.1305T>C
XM_017016912.2:c.695-579T>C	XP_016872401.1:n.695-579T>C
NM_005097.4:c.1041T>C MANE Select	NP_005088.1:p.Val347=
NM_001308275.2:c.839-579T>C	NP_001295204.1:n.839-579T>C
NM_001308276.2:c.897T>C	NP_001295205.1:p.Val299=
NR_131777.2:n.1178T>C