Canonical Allele Identifier: CA470800146

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553088G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793331G>C , CM000672.2:g.93793331G>C	GRCh38
NC_000010.10:g.95553088G>C , CM000672.1:g.95553088G>C	GRCh37
NC_000010.9:g.95543078G>C	NCBI36
NG_011832.1:g.40523G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.819G>C MANE Select	ENSP00000360472.4:p.Arg273=
ENST00000485458.3:n.4795G>C
ENST00000635953.1:c.819G>C	ENSP00000490058.1:p.Arg273=
ENST00000636155.1:c.819G>C	ENSP00000490355.1:p.Arg273=
ENST00000636232.1:c.*605G>C	ENSP00000490325.1:n.*605G>C
ENST00000636754.1:c.*661G>C	ENSP00000489781.1:n.*661G>C
ENST00000636946.1:c.*988G>C	ENSP00000490654.1:n.*988G>C
ENST00000637037.1:c.*409G>C	ENSP00000490860.1:n.*409G>C
ENST00000637347.1:n.680G>C
ENST00000637611.1:c.*375G>C	ENSP00000489682.1:n.*375G>C
ENST00000637689.1:c.-553G>C	ENSP00000490496.1:n.-553G>C
ENST00000637925.1:c.*414G>C	ENSP00000489763.1:n.*414G>C
ENST00000638049.1:c.*577G>C	ENSP00000490597.1:n.*577G>C
ENST00000676175.1:n.2558G>C
ENST00000371413.4:c.819G>C	ENSP00000360467.3:p.Arg273=
ENST00000371418.8:c.819G>C	ENSP00000360472.4:p.Arg273=
ENST00000626307.1:n.4734G>C
ENST00000626946.1:n.489G>C
ENST00000627420.2:c.*528G>C	ENSP00000487116.1:n.*528G>C
ENST00000629035.2:c.747G>C	ENSP00000486908.1:p.Arg249=
ENST00000630047.2:c.675G>C	ENSP00000485917.1:p.Arg225=
ENST00000630487.2:c.*609G>C	ENSP00000486859.1:n.*609G>C
NM_001308275.1:c.819G>C	NP_001295204.1:p.Arg273=
NM_001308276.1:c.675G>C	NP_001295205.1:p.Arg225=
NM_005097.2:c.819G>C	NP_005088.1:p.Arg273=
NM_005097.3:c.819G>C	NP_005088.1:p.Arg273=
NR_131777.1:n.1083G>C
XM_017016911.2:c.819G>C	XP_016872400.1:p.Arg273=
XM_017016912.2:c.675G>C	XP_016872401.1:p.Arg225=
NM_005097.4:c.819G>C MANE Select	NP_005088.1:p.Arg273=
NM_001308275.2:c.819G>C	NP_001295204.1:p.Arg273=
NM_001308276.2:c.675G>C	NP_001295205.1:p.Arg225=
NR_131777.2:n.956G>C