Canonical Allele Identifier: CA1928787494

Gene: LGI1

Linked Data

• dbSNP Id: rs2059950443
• gnomAD v4: 10-93793134-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793134C>T , CM000672.2:g.93793134C>T	GRCh38
NC_000010.10:g.95552891C>T , CM000672.1:g.95552891C>T	GRCh37
NC_000010.9:g.95542881C>T	NCBI36
NG_011832.1:g.40326C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.674-52C>T MANE Select	ENSP00000360472.4:n.674-52C>T
ENST00000485458.3:n.4650-52C>T
ENST00000635953.1:c.674-52C>T	ENSP00000490058.1:n.674-52C>T
ENST00000636155.1:c.674-52C>T	ENSP00000490355.1:n.674-52C>T
ENST00000636232.1:c.*460-52C>T	ENSP00000490325.1:n.*460-52C>T
ENST00000636754.1:c.*516-52C>T	ENSP00000489781.1:n.*516-52C>T
ENST00000636946.1:c.*843-52C>T	ENSP00000490654.1:n.*843-52C>T
ENST00000637037.1:c.*264-52C>T	ENSP00000490860.1:n.*264-52C>T
ENST00000637347.1:n.535-52C>T
ENST00000637611.1:c.*230-52C>T	ENSP00000489682.1:n.*230-52C>T
ENST00000637689.1:c.-698-52C>T	ENSP00000490496.1:n.-698-52C>T
ENST00000637925.1:c.*269-52C>T	ENSP00000489763.1:n.*269-52C>T
ENST00000638049.1:c.*432-52C>T	ENSP00000490597.1:n.*432-52C>T
ENST00000676175.1:n.2413-52C>T
ENST00000371413.4:c.674-52C>T	ENSP00000360467.3:n.674-52C>T
ENST00000371418.8:c.674-52C>T	ENSP00000360472.4:n.674-52C>T
ENST00000626307.1:n.4589-52C>T
ENST00000626946.1:n.292C>T
ENST00000627420.2:c.*383-52C>T	ENSP00000487116.1:n.*383-52C>T
ENST00000629035.2:c.602-52C>T	ENSP00000486908.1:n.602-52C>T
ENST00000630047.2:c.530-52C>T	ENSP00000485917.1:n.530-52C>T
ENST00000630412.1:n.462-52C>T
ENST00000630487.2:c.*464-52C>T	ENSP00000486859.1:n.*464-52C>T
NM_001308275.1:c.674-52C>T	NP_001295204.1:n.674-52C>T
NM_001308276.1:c.530-52C>T	NP_001295205.1:n.530-52C>T
NM_005097.2:c.674-52C>T	NP_005088.1:n.674-52C>T
NM_005097.3:c.674-52C>T	NP_005088.1:n.674-52C>T
NR_131777.1:n.938-52C>T
XM_017016911.2:c.674-52C>T	XP_016872400.1:n.674-52C>T
XM_017016912.2:c.530-52C>T	XP_016872401.1:n.530-52C>T
NM_005097.4:c.674-52C>T MANE Select	NP_005088.1:n.674-52C>T
NM_001308275.2:c.674-52C>T	NP_001295204.1:n.674-52C>T
NM_001308276.2:c.530-52C>T	NP_001295205.1:n.530-52C>T
NR_131777.2:n.811-52C>T