Canonical Allele Identifier: CA470800098

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552992T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793235T>C , CM000672.2:g.93793235T>C	GRCh38
NC_000010.10:g.95552992T>C , CM000672.1:g.95552992T>C	GRCh37
NC_000010.9:g.95542982T>C	NCBI36
NG_011832.1:g.40427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.723T>C MANE Select	ENSP00000360472.4:p.Thr241=
ENST00000485458.3:n.4699T>C
ENST00000635953.1:c.723T>C	ENSP00000490058.1:p.Thr241=
ENST00000636155.1:c.723T>C	ENSP00000490355.1:p.Thr241=
ENST00000636232.1:c.*509T>C	ENSP00000490325.1:n.*509T>C
ENST00000636754.1:c.*565T>C	ENSP00000489781.1:n.*565T>C
ENST00000636946.1:c.*892T>C	ENSP00000490654.1:n.*892T>C
ENST00000637037.1:c.*313T>C	ENSP00000490860.1:n.*313T>C
ENST00000637347.1:n.584T>C
ENST00000637611.1:c.*279T>C	ENSP00000489682.1:n.*279T>C
ENST00000637689.1:c.-649T>C	ENSP00000490496.1:n.-649T>C
ENST00000637925.1:c.*318T>C	ENSP00000489763.1:n.*318T>C
ENST00000638049.1:c.*481T>C	ENSP00000490597.1:n.*481T>C
ENST00000676175.1:n.2462T>C
ENST00000371413.4:c.723T>C	ENSP00000360467.3:p.Thr241=
ENST00000371418.8:c.723T>C	ENSP00000360472.4:p.Thr241=
ENST00000626307.1:n.4638T>C
ENST00000626946.1:n.393T>C
ENST00000627420.2:c.*432T>C	ENSP00000487116.1:n.*432T>C
ENST00000629035.2:c.651T>C	ENSP00000486908.1:p.Thr217=
ENST00000630047.2:c.579T>C	ENSP00000485917.1:p.Thr193=
ENST00000630412.1:n.511T>C
ENST00000630487.2:c.*513T>C	ENSP00000486859.1:n.*513T>C
NM_001308275.1:c.723T>C	NP_001295204.1:p.Thr241=
NM_001308276.1:c.579T>C	NP_001295205.1:p.Thr193=
NM_005097.2:c.723T>C	NP_005088.1:p.Thr241=
NM_005097.3:c.723T>C	NP_005088.1:p.Thr241=
NR_131777.1:n.987T>C
XM_017016911.2:c.723T>C	XP_016872400.1:p.Thr241=
XM_017016912.2:c.579T>C	XP_016872401.1:p.Thr193=
NM_005097.4:c.723T>C MANE Select	NP_005088.1:p.Thr241=
NM_001308275.2:c.723T>C	NP_001295204.1:p.Thr241=
NM_001308276.2:c.579T>C	NP_001295205.1:p.Thr193=
NR_131777.2:n.860T>C