Canonical Allele Identifier: CA470985125

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556924T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797167T>C , CM000672.2:g.93797167T>C	GRCh38
NC_000010.10:g.95556924T>C , CM000672.1:g.95556924T>C	GRCh37
NC_000010.9:g.95546914T>C	NCBI36
NG_011832.1:g.44359T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1038T>C MANE Select	ENSP00000360472.4:p.Phe346=
ENST00000485458.3:n.5014T>C
ENST00000635804.1:n.472T>C
ENST00000635953.1:c.*460T>C	ENSP00000490058.1:n.*460T>C
ENST00000636155.1:c.838+3817T>C	ENSP00000490355.1:n.838+3817T>C
ENST00000636232.1:c.*824T>C	ENSP00000490325.1:n.*824T>C
ENST00000636754.1:c.*880T>C	ENSP00000489781.1:n.*880T>C
ENST00000636946.1:c.*1008-582T>C	ENSP00000490654.1:n.*1008-582T>C
ENST00000637037.1:c.*628T>C	ENSP00000490860.1:n.*628T>C
ENST00000637347.1:n.899T>C
ENST00000637611.1:c.*594T>C	ENSP00000489682.1:n.*594T>C
ENST00000637689.1:c.-334T>C	ENSP00000490496.1:n.-334T>C
ENST00000637925.1:c.*633T>C	ENSP00000489763.1:n.*633T>C
ENST00000638049.1:c.*796T>C	ENSP00000490597.1:n.*796T>C
ENST00000676175.1:n.2777T>C
ENST00000371413.4:c.839-582T>C	ENSP00000360467.3:n.839-582T>C
ENST00000371418.8:c.1038T>C	ENSP00000360472.4:p.Phe346=
ENST00000626307.1:n.4953T>C
ENST00000627420.2:c.*747T>C	ENSP00000487116.1:n.*747T>C
ENST00000629035.2:c.966T>C	ENSP00000486908.1:p.Phe322=
ENST00000630047.2:c.894T>C	ENSP00000485917.1:p.Phe298=
NM_001308275.1:c.839-582T>C	NP_001295204.1:n.839-582T>C
NM_001308276.1:c.894T>C	NP_001295205.1:p.Phe298=
NM_005097.2:c.1038T>C	NP_005088.1:p.Phe346=
NM_005097.3:c.1038T>C	NP_005088.1:p.Phe346=
NR_131777.1:n.1302T>C
XM_017016912.2:c.695-582T>C	XP_016872401.1:n.695-582T>C
NM_005097.4:c.1038T>C MANE Select	NP_005088.1:p.Phe346=
NM_001308275.2:c.839-582T>C	NP_001295204.1:n.839-582T>C
NM_001308276.2:c.894T>C	NP_001295205.1:p.Phe298=
NR_131777.2:n.1175T>C