Canonical Allele Identifier: CA470800083

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793211T>A , CM000672.2:g.93793211T>A	GRCh38
NC_000010.10:g.95552968T>A , CM000672.1:g.95552968T>A	GRCh37
NC_000010.9:g.95542958T>A	NCBI36
NG_011832.1:g.40403T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.699T>A MANE Select	ENSP00000360472.4:p.Pro233=
ENST00000485458.3:n.4675T>A
ENST00000635953.1:c.699T>A	ENSP00000490058.1:p.Pro233=
ENST00000636155.1:c.699T>A	ENSP00000490355.1:p.Pro233=
ENST00000636232.1:c.*485T>A	ENSP00000490325.1:n.*485T>A
ENST00000636754.1:c.*541T>A	ENSP00000489781.1:n.*541T>A
ENST00000636946.1:c.*868T>A	ENSP00000490654.1:n.*868T>A
ENST00000637037.1:c.*289T>A	ENSP00000490860.1:n.*289T>A
ENST00000637347.1:n.560T>A
ENST00000637611.1:c.*255T>A	ENSP00000489682.1:n.*255T>A
ENST00000637689.1:c.-673T>A	ENSP00000490496.1:n.-673T>A
ENST00000637925.1:c.*294T>A	ENSP00000489763.1:n.*294T>A
ENST00000638049.1:c.*457T>A	ENSP00000490597.1:n.*457T>A
ENST00000676175.1:n.2438T>A
ENST00000371413.4:c.699T>A	ENSP00000360467.3:p.Pro233=
ENST00000371418.8:c.699T>A	ENSP00000360472.4:p.Pro233=
ENST00000626307.1:n.4614T>A
ENST00000626946.1:n.369T>A
ENST00000627420.2:c.*408T>A	ENSP00000487116.1:n.*408T>A
ENST00000629035.2:c.627T>A	ENSP00000486908.1:p.Pro209=
ENST00000630047.2:c.555T>A	ENSP00000485917.1:p.Pro185=
ENST00000630412.1:n.487T>A
ENST00000630487.2:c.*489T>A	ENSP00000486859.1:n.*489T>A
NM_001308275.1:c.699T>A	NP_001295204.1:p.Pro233=
NM_001308276.1:c.555T>A	NP_001295205.1:p.Pro185=
NM_005097.2:c.699T>A	NP_005088.1:p.Pro233=
NM_005097.3:c.699T>A	NP_005088.1:p.Pro233=
NR_131777.1:n.963T>A
XM_017016911.2:c.699T>A	XP_016872400.1:p.Pro233=
XM_017016912.2:c.555T>A	XP_016872401.1:p.Pro185=
NM_005097.4:c.699T>A MANE Select	NP_005088.1:p.Pro233=
NM_001308275.2:c.699T>A	NP_001295204.1:p.Pro233=
NM_001308276.2:c.555T>A	NP_001295205.1:p.Pro185=
NR_131777.2:n.836T>A