Canonical Allele Identifier: CA377623991

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552972C>A (hg19) ; chr10:g.93793215C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793215C>A , CM000672.2:g.93793215C>A	GRCh38
NC_000010.10:g.95552972C>A , CM000672.1:g.95552972C>A	GRCh37
NC_000010.9:g.95542962C>A	NCBI36
NG_011832.1:g.40407C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.703C>A MANE Select	ENSP00000360472.4:p.Gln235Lys
ENST00000485458.3:n.4679C>A
ENST00000635953.1:c.703C>A	ENSP00000490058.1:p.Gln235Lys
ENST00000636155.1:c.703C>A	ENSP00000490355.1:p.Gln235Lys
ENST00000636232.1:c.*489C>A	ENSP00000490325.1:n.*489C>A
ENST00000636754.1:c.*545C>A	ENSP00000489781.1:n.*545C>A
ENST00000636946.1:c.*872C>A	ENSP00000490654.1:n.*872C>A
ENST00000637037.1:c.*293C>A	ENSP00000490860.1:n.*293C>A
ENST00000637347.1:n.564C>A
ENST00000637611.1:c.*259C>A	ENSP00000489682.1:n.*259C>A
ENST00000637689.1:c.-669C>A	ENSP00000490496.1:n.-669C>A
ENST00000637925.1:c.*298C>A	ENSP00000489763.1:n.*298C>A
ENST00000638049.1:c.*461C>A	ENSP00000490597.1:n.*461C>A
ENST00000676175.1:n.2442C>A
ENST00000371413.4:c.703C>A	ENSP00000360467.3:p.Gln235Lys
ENST00000371418.8:c.703C>A	ENSP00000360472.4:p.Gln235Lys
ENST00000626307.1:n.4618C>A
ENST00000626946.1:n.373C>A
ENST00000627420.2:c.*412C>A	ENSP00000487116.1:n.*412C>A
ENST00000629035.2:c.631C>A	ENSP00000486908.1:p.Gln211Lys
ENST00000630047.2:c.559C>A	ENSP00000485917.1:p.Gln187Lys
ENST00000630412.1:n.491C>A
ENST00000630487.2:c.*493C>A	ENSP00000486859.1:n.*493C>A
NM_001308275.1:c.703C>A	NP_001295204.1:p.Gln235Lys
NM_001308276.1:c.559C>A	NP_001295205.1:p.Gln187Lys
NM_005097.2:c.703C>A	NP_005088.1:p.Gln235Lys
NM_005097.3:c.703C>A	NP_005088.1:p.Gln235Lys
NR_131777.1:n.967C>A
XM_017016911.2:c.703C>A	XP_016872400.1:p.Gln235Lys
XM_017016912.2:c.559C>A	XP_016872401.1:p.Gln187Lys
NM_005097.4:c.703C>A MANE Select	NP_005088.1:p.Gln235Lys
NM_001308275.2:c.703C>A	NP_001295204.1:p.Gln235Lys
NM_001308276.2:c.559C>A	NP_001295205.1:p.Gln187Lys
NR_131777.2:n.840C>A