Canonical Allele Identifier: CA377623956

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552962C>G (hg19) ; chr10:g.93793205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793205C>G , CM000672.2:g.93793205C>G	GRCh38
NC_000010.10:g.95552962C>G , CM000672.1:g.95552962C>G	GRCh37
NC_000010.9:g.95542952C>G	NCBI36
NG_011832.1:g.40397C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.693C>G MANE Select	ENSP00000360472.4:p.Asp231Glu
ENST00000485458.3:n.4669C>G
ENST00000635953.1:c.693C>G	ENSP00000490058.1:p.Asp231Glu
ENST00000636155.1:c.693C>G	ENSP00000490355.1:p.Asp231Glu
ENST00000636232.1:c.*479C>G	ENSP00000490325.1:n.*479C>G
ENST00000636754.1:c.*535C>G	ENSP00000489781.1:n.*535C>G
ENST00000636946.1:c.*862C>G	ENSP00000490654.1:n.*862C>G
ENST00000637037.1:c.*283C>G	ENSP00000490860.1:n.*283C>G
ENST00000637347.1:n.554C>G
ENST00000637611.1:c.*249C>G	ENSP00000489682.1:n.*249C>G
ENST00000637689.1:c.-679C>G	ENSP00000490496.1:n.-679C>G
ENST00000637925.1:c.*288C>G	ENSP00000489763.1:n.*288C>G
ENST00000638049.1:c.*451C>G	ENSP00000490597.1:n.*451C>G
ENST00000676175.1:n.2432C>G
ENST00000371413.4:c.693C>G	ENSP00000360467.3:p.Asp231Glu
ENST00000371418.8:c.693C>G	ENSP00000360472.4:p.Asp231Glu
ENST00000626307.1:n.4608C>G
ENST00000626946.1:n.363C>G
ENST00000627420.2:c.*402C>G	ENSP00000487116.1:n.*402C>G
ENST00000629035.2:c.621C>G	ENSP00000486908.1:p.Asp207Glu
ENST00000630047.2:c.549C>G	ENSP00000485917.1:p.Asp183Glu
ENST00000630412.1:n.481C>G
ENST00000630487.2:c.*483C>G	ENSP00000486859.1:n.*483C>G
NM_001308275.1:c.693C>G	NP_001295204.1:p.Asp231Glu
NM_001308276.1:c.549C>G	NP_001295205.1:p.Asp183Glu
NM_005097.2:c.693C>G	NP_005088.1:p.Asp231Glu
NM_005097.3:c.693C>G	NP_005088.1:p.Asp231Glu
NR_131777.1:n.957C>G
XM_017016911.2:c.693C>G	XP_016872400.1:p.Asp231Glu
XM_017016912.2:c.549C>G	XP_016872401.1:p.Asp183Glu
NM_005097.4:c.693C>G MANE Select	NP_005088.1:p.Asp231Glu
NM_001308275.2:c.693C>G	NP_001295204.1:p.Asp231Glu
NM_001308276.2:c.549C>G	NP_001295205.1:p.Asp183Glu
NR_131777.2:n.830C>G