Canonical Allele Identifier: CA377624178

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553014T>C (hg19) ; chr10:g.93793257T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793257T>C , CM000672.2:g.93793257T>C	GRCh38
NC_000010.10:g.95553014T>C , CM000672.1:g.95553014T>C	GRCh37
NC_000010.9:g.95543004T>C	NCBI36
NG_011832.1:g.40449T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.745T>C MANE Select	ENSP00000360472.4:p.Tyr249His
ENST00000485458.3:n.4721T>C
ENST00000635953.1:c.745T>C	ENSP00000490058.1:p.Tyr249His
ENST00000636155.1:c.745T>C	ENSP00000490355.1:p.Tyr249His
ENST00000636232.1:c.*531T>C	ENSP00000490325.1:n.*531T>C
ENST00000636754.1:c.*587T>C	ENSP00000489781.1:n.*587T>C
ENST00000636946.1:c.*914T>C	ENSP00000490654.1:n.*914T>C
ENST00000637037.1:c.*335T>C	ENSP00000490860.1:n.*335T>C
ENST00000637347.1:n.606T>C
ENST00000637611.1:c.*301T>C	ENSP00000489682.1:n.*301T>C
ENST00000637689.1:c.-627T>C	ENSP00000490496.1:n.-627T>C
ENST00000637925.1:c.*340T>C	ENSP00000489763.1:n.*340T>C
ENST00000638049.1:c.*503T>C	ENSP00000490597.1:n.*503T>C
ENST00000676175.1:n.2484T>C
ENST00000371413.4:c.745T>C	ENSP00000360467.3:p.Tyr249His
ENST00000371418.8:c.745T>C	ENSP00000360472.4:p.Tyr249His
ENST00000626307.1:n.4660T>C
ENST00000626946.1:n.415T>C
ENST00000627420.2:c.*454T>C	ENSP00000487116.1:n.*454T>C
ENST00000629035.2:c.673T>C	ENSP00000486908.1:p.Tyr225His
ENST00000630047.2:c.601T>C	ENSP00000485917.1:p.Tyr201His
ENST00000630412.1:n.533T>C
ENST00000630487.2:c.*535T>C	ENSP00000486859.1:n.*535T>C
NM_001308275.1:c.745T>C	NP_001295204.1:p.Tyr249His
NM_001308276.1:c.601T>C	NP_001295205.1:p.Tyr201His
NM_005097.2:c.745T>C	NP_005088.1:p.Tyr249His
NM_005097.3:c.745T>C	NP_005088.1:p.Tyr249His
NR_131777.1:n.1009T>C
XM_017016911.2:c.745T>C	XP_016872400.1:p.Tyr249His
XM_017016912.2:c.601T>C	XP_016872401.1:p.Tyr201His
NM_005097.4:c.745T>C MANE Select	NP_005088.1:p.Tyr249His
NM_001308275.2:c.745T>C	NP_001295204.1:p.Tyr249His
NM_001308276.2:c.601T>C	NP_001295205.1:p.Tyr201His
NR_131777.2:n.882T>C