Canonical Allele Identifier: CA377623875

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552943A>T (hg19) ; chr10:g.93793186A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793186A>T , CM000672.2:g.93793186A>T	GRCh38
NC_000010.10:g.95552943A>T , CM000672.1:g.95552943A>T	GRCh37
NC_000010.9:g.95542933A>T	NCBI36
NG_011832.1:g.40378A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.674A>T MANE Select	ENSP00000360472.4:p.Glu225Val
ENST00000485458.3:n.4650A>T
ENST00000635953.1:c.674A>T	ENSP00000490058.1:p.Glu225Val
ENST00000636155.1:c.674A>T	ENSP00000490355.1:p.Glu225Val
ENST00000636232.1:c.*460A>T	ENSP00000490325.1:n.*460A>T
ENST00000636754.1:c.*516A>T	ENSP00000489781.1:n.*516A>T
ENST00000636946.1:c.*843A>T	ENSP00000490654.1:n.*843A>T
ENST00000637037.1:c.*264A>T	ENSP00000490860.1:n.*264A>T
ENST00000637347.1:n.535A>T
ENST00000637611.1:c.*230A>T	ENSP00000489682.1:n.*230A>T
ENST00000637689.1:c.-698A>T	ENSP00000490496.1:n.-698A>T
ENST00000637925.1:c.*269A>T	ENSP00000489763.1:n.*269A>T
ENST00000638049.1:c.*432A>T	ENSP00000490597.1:n.*432A>T
ENST00000676175.1:n.2413A>T
ENST00000371413.4:c.674A>T	ENSP00000360467.3:p.Glu225Val
ENST00000371418.8:c.674A>T	ENSP00000360472.4:p.Glu225Val
ENST00000626307.1:n.4589A>T
ENST00000626946.1:n.344A>T
ENST00000627420.2:c.*383A>T	ENSP00000487116.1:n.*383A>T
ENST00000629035.2:c.602A>T	ENSP00000486908.1:p.Glu201Val
ENST00000630047.2:c.530A>T	ENSP00000485917.1:p.Glu177Val
ENST00000630412.1:n.462A>T
ENST00000630487.2:c.*464A>T	ENSP00000486859.1:n.*464A>T
NM_001308275.1:c.674A>T	NP_001295204.1:p.Glu225Val
NM_001308276.1:c.530A>T	NP_001295205.1:p.Glu177Val
NM_005097.2:c.674A>T	NP_005088.1:p.Glu225Val
NM_005097.3:c.674A>T	NP_005088.1:p.Glu225Val
NR_131777.1:n.938A>T
XM_017016911.2:c.674A>T	XP_016872400.1:p.Glu225Val
XM_017016912.2:c.530A>T	XP_016872401.1:p.Glu177Val
NM_005097.4:c.674A>T MANE Select	NP_005088.1:p.Glu225Val
NM_001308275.2:c.674A>T	NP_001295204.1:p.Glu225Val
NM_001308276.2:c.530A>T	NP_001295205.1:p.Glu177Val
NR_131777.2:n.811A>T