Canonical Allele Identifier: CA377624255

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553032C>G (hg19) ; chr10:g.93793275C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793275C>G , CM000672.2:g.93793275C>G	GRCh38
NC_000010.10:g.95553032C>G , CM000672.1:g.95553032C>G	GRCh37
NC_000010.9:g.95543022C>G	NCBI36
NG_011832.1:g.40467C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.763C>G MANE Select	ENSP00000360472.4:p.Pro255Ala
ENST00000485458.3:n.4739C>G
ENST00000635953.1:c.763C>G	ENSP00000490058.1:p.Pro255Ala
ENST00000636155.1:c.763C>G	ENSP00000490355.1:p.Pro255Ala
ENST00000636232.1:c.*549C>G	ENSP00000490325.1:n.*549C>G
ENST00000636754.1:c.*605C>G	ENSP00000489781.1:n.*605C>G
ENST00000636946.1:c.*932C>G	ENSP00000490654.1:n.*932C>G
ENST00000637037.1:c.*353C>G	ENSP00000490860.1:n.*353C>G
ENST00000637347.1:n.624C>G
ENST00000637611.1:c.*319C>G	ENSP00000489682.1:n.*319C>G
ENST00000637689.1:c.-609C>G	ENSP00000490496.1:n.-609C>G
ENST00000637925.1:c.*358C>G	ENSP00000489763.1:n.*358C>G
ENST00000638049.1:c.*521C>G	ENSP00000490597.1:n.*521C>G
ENST00000676175.1:n.2502C>G
ENST00000371413.4:c.763C>G	ENSP00000360467.3:p.Pro255Ala
ENST00000371418.8:c.763C>G	ENSP00000360472.4:p.Pro255Ala
ENST00000626307.1:n.4678C>G
ENST00000626946.1:n.433C>G
ENST00000627420.2:c.*472C>G	ENSP00000487116.1:n.*472C>G
ENST00000629035.2:c.691C>G	ENSP00000486908.1:p.Pro231Ala
ENST00000630047.2:c.619C>G	ENSP00000485917.1:p.Pro207Ala
ENST00000630487.2:c.*553C>G	ENSP00000486859.1:n.*553C>G
NM_001308275.1:c.763C>G	NP_001295204.1:p.Pro255Ala
NM_001308276.1:c.619C>G	NP_001295205.1:p.Pro207Ala
NM_005097.2:c.763C>G	NP_005088.1:p.Pro255Ala
NM_005097.3:c.763C>G	NP_005088.1:p.Pro255Ala
NR_131777.1:n.1027C>G
XM_017016911.2:c.763C>G	XP_016872400.1:p.Pro255Ala
XM_017016912.2:c.619C>G	XP_016872401.1:p.Pro207Ala
NM_005097.4:c.763C>G MANE Select	NP_005088.1:p.Pro255Ala
NM_001308275.2:c.763C>G	NP_001295204.1:p.Pro255Ala
NM_001308276.2:c.619C>G	NP_001295205.1:p.Pro207Ala
NR_131777.2:n.900C>G