Canonical Allele Identifier: CA2610226547

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793092-TCTCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793093_93793097del , CM000672.2:g.93793093_93793097del	GRCh38
NC_000010.10:g.95552850_95552854del , CM000672.1:g.95552850_95552854del	GRCh37
NC_000010.9:g.95542840_95542844del	NCBI36
NG_011832.1:g.40285_40289del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.674-93_674-89del MANE Select	ENSP00000360472.4:n.674-93_674-89del
ENST00000485458.3:n.4650-93_4650-89del
ENST00000635953.1:c.674-93_674-89del	ENSP00000490058.1:n.674-93_674-89del
ENST00000636155.1:c.674-93_674-89del	ENSP00000490355.1:n.674-93_674-89del
ENST00000636232.1:c.*460-93_*460-89del	ENSP00000490325.1:n.*460-93_*460-89del
ENST00000636754.1:c.*516-93_*516-89del	ENSP00000489781.1:n.*516-93_*516-89del
ENST00000636946.1:c.*843-93_*843-89del	ENSP00000490654.1:n.*843-93_*843-89del
ENST00000637037.1:c.*264-93_*264-89del	ENSP00000490860.1:n.*264-93_*264-89del
ENST00000637347.1:n.535-93_535-89del
ENST00000637611.1:c.*230-93_*230-89del	ENSP00000489682.1:n.*230-93_*230-89del
ENST00000637689.1:c.-698-93_-698-89del	ENSP00000490496.1:n.-698-93_-698-89del
ENST00000637925.1:c.*269-93_*269-89del	ENSP00000489763.1:n.*269-93_*269-89del
ENST00000638049.1:c.*432-93_*432-89del	ENSP00000490597.1:n.*432-93_*432-89del
ENST00000676175.1:n.2413-93_2413-89del
ENST00000371413.4:c.674-93_674-89del	ENSP00000360467.3:n.674-93_674-89del
ENST00000371418.8:c.674-93_674-89del	ENSP00000360472.4:n.674-93_674-89del
ENST00000626307.1:n.4589-93_4589-89del
ENST00000626946.1:n.251_255del
ENST00000627420.2:c.*383-93_*383-89del	ENSP00000487116.1:n.*383-93_*383-89del
ENST00000629035.2:c.602-93_602-89del	ENSP00000486908.1:n.602-93_602-89del
ENST00000630047.2:c.530-93_530-89del	ENSP00000485917.1:n.530-93_530-89del
ENST00000630412.1:n.462-93_462-89del
ENST00000630487.2:c.*464-93_*464-89del	ENSP00000486859.1:n.*464-93_*464-89del
NM_001308275.1:c.674-93_674-89del	NP_001295204.1:n.674-93_674-89del
NM_001308276.1:c.530-93_530-89del	NP_001295205.1:n.530-93_530-89del
NM_005097.2:c.674-93_674-89del	NP_005088.1:n.674-93_674-89del
NM_005097.3:c.674-93_674-89del	NP_005088.1:n.674-93_674-89del
NR_131777.1:n.938-93_938-89del
XM_017016911.2:c.674-93_674-89del	XP_016872400.1:n.674-93_674-89del
XM_017016912.2:c.530-93_530-89del	XP_016872401.1:n.530-93_530-89del
NM_005097.4:c.674-93_674-89del MANE Select	NP_005088.1:n.674-93_674-89del
NM_001308275.2:c.674-93_674-89del	NP_001295204.1:n.674-93_674-89del
NM_001308276.2:c.530-93_530-89del	NP_001295205.1:n.530-93_530-89del
NR_131777.2:n.811-93_811-89del