Canonical Allele Identifier: CA1928787498

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793144_93793145delinsAG , CM000672.2:g.93793144_93793145delinsAG	GRCh38
NC_000010.10:g.95552901_95552902delinsAG , CM000672.1:g.95552901_95552902delinsAG	GRCh37
NC_000010.9:g.95542891_95542892delinsAG	NCBI36
NG_011832.1:g.40336_40337delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.674-42_674-41delinsAG MANE Select	ENSP00000360472.4:n.674-42_674-41delinsAG
ENST00000485458.3:n.4650-42_4650-41delinsAG
ENST00000635953.1:c.674-42_674-41delinsAG	ENSP00000490058.1:n.674-42_674-41delinsAG
ENST00000636155.1:c.674-42_674-41delinsAG	ENSP00000490355.1:n.674-42_674-41delinsAG
ENST00000636232.1:c.*460-42_*460-41delinsAG	ENSP00000490325.1:n.*460-42_*460-41delinsAG
ENST00000636754.1:c.*516-42_*516-41delinsAG	ENSP00000489781.1:n.*516-42_*516-41delinsAG
ENST00000636946.1:c.*843-42_*843-41delinsAG	ENSP00000490654.1:n.*843-42_*843-41delinsAG
ENST00000637037.1:c.*264-42_*264-41delinsAG	ENSP00000490860.1:n.*264-42_*264-41delinsAG
ENST00000637347.1:n.535-42_535-41delinsAG
ENST00000637611.1:c.*230-42_*230-41delinsAG	ENSP00000489682.1:n.*230-42_*230-41delinsAG
ENST00000637689.1:c.-698-42_-698-41delinsAG	ENSP00000490496.1:n.-698-42_-698-41delinsAG
ENST00000637925.1:c.*269-42_*269-41delinsAG	ENSP00000489763.1:n.*269-42_*269-41delinsAG
ENST00000638049.1:c.*432-42_*432-41delinsAG	ENSP00000490597.1:n.*432-42_*432-41delinsAG
ENST00000676175.1:n.2413-42_2413-41delinsAG
ENST00000371413.4:c.674-42_674-41delinsAG	ENSP00000360467.3:n.674-42_674-41delinsAG
ENST00000371418.8:c.674-42_674-41delinsAG	ENSP00000360472.4:n.674-42_674-41delinsAG
ENST00000626307.1:n.4589-42_4589-41delinsAG
ENST00000626946.1:n.302_303delinsAG
ENST00000627420.2:c.*383-42_*383-41delinsAG	ENSP00000487116.1:n.*383-42_*383-41delinsAG
ENST00000629035.2:c.602-42_602-41delinsAG	ENSP00000486908.1:n.602-42_602-41delinsAG
ENST00000630047.2:c.530-42_530-41delinsAG	ENSP00000485917.1:n.530-42_530-41delinsAG
ENST00000630412.1:n.462-42_462-41delinsAG
ENST00000630487.2:c.*464-42_*464-41delinsAG	ENSP00000486859.1:n.*464-42_*464-41delinsAG
NM_001308275.1:c.674-42_674-41delinsAG	NP_001295204.1:n.674-42_674-41delinsAG
NM_001308276.1:c.530-42_530-41delinsAG	NP_001295205.1:n.530-42_530-41delinsAG
NM_005097.2:c.674-42_674-41delinsAG	NP_005088.1:n.674-42_674-41delinsAG
NM_005097.3:c.674-42_674-41delinsAG	NP_005088.1:n.674-42_674-41delinsAG
NR_131777.1:n.938-42_938-41delinsAG
XM_017016911.2:c.674-42_674-41delinsAG	XP_016872400.1:n.674-42_674-41delinsAG
XM_017016912.2:c.530-42_530-41delinsAG	XP_016872401.1:n.530-42_530-41delinsAG
NM_005097.4:c.674-42_674-41delinsAG MANE Select	NP_005088.1:n.674-42_674-41delinsAG
NM_001308275.2:c.674-42_674-41delinsAG	NP_001295204.1:n.674-42_674-41delinsAG
NM_001308276.2:c.530-42_530-41delinsAG	NP_001295205.1:n.530-42_530-41delinsAG
NR_131777.2:n.811-42_811-41delinsAG