Canonical Allele Identifier: CA2789043553

Gene: LGI1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793048_93793049del , CM000672.2:g.93793048_93793049del	GRCh38
NC_000010.10:g.95552805_95552806del , CM000672.1:g.95552805_95552806del	GRCh37
NC_000010.9:g.95542795_95542796del	NCBI36
NG_011832.1:g.40240_40241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.673+136_674-137del MANE Select	ENSP00000360472.4:n.673+136_674-137del
ENST00000485458.3:n.4649+136_4650-137del
ENST00000635953.1:c.673+136_674-137del	ENSP00000490058.1:n.673+136_674-137del
ENST00000636155.1:c.673+136_674-137del	ENSP00000490355.1:n.673+136_674-137del
ENST00000636232.1:c.*459+136_*460-137del	ENSP00000490325.1:n.*459+136_*460-137del
ENST00000636754.1:c.*515+136_*516-137del	ENSP00000489781.1:n.*515+136_*516-137del
ENST00000636946.1:c.*842+136_*843-137del	ENSP00000490654.1:n.*842+136_*843-137del
ENST00000637037.1:c.*263+136_*264-137del	ENSP00000490860.1:n.*263+136_*264-137del
ENST00000637347.1:n.534+136_535-137del
ENST00000637611.1:c.*229+136_*230-137del	ENSP00000489682.1:n.*229+136_*230-137del
ENST00000637689.1:c.-699+136_-698-137del	ENSP00000490496.1:n.-699+136_-698-137del
ENST00000637925.1:c.*268+136_*269-137del	ENSP00000489763.1:n.*268+136_*269-137del
ENST00000638049.1:c.*431+136_*432-137del	ENSP00000490597.1:n.*431+136_*432-137del
ENST00000676175.1:n.2412+136_2413-137del
ENST00000371413.4:c.673+136_674-137del	ENSP00000360467.3:n.673+136_674-137del
ENST00000371418.8:c.673+136_674-137del	ENSP00000360472.4:n.673+136_674-137del
ENST00000626307.1:n.4588+136_4589-137del
ENST00000626946.1:n.206_207del
ENST00000627420.2:c.*382+136_*383-137del	ENSP00000487116.1:n.*382+136_*383-137del
ENST00000629035.2:c.601+136_602-137del	ENSP00000486908.1:n.601+136_602-137del
ENST00000630047.2:c.529+136_530-137del	ENSP00000485917.1:n.529+136_530-137del
ENST00000630412.1:n.461+136_462-137del
ENST00000630487.2:c.*463+136_*464-137del	ENSP00000486859.1:n.*463+136_*464-137del
NM_001308275.1:c.673+136_674-137del	NP_001295204.1:n.673+136_674-137del
NM_001308276.1:c.529+136_530-137del	NP_001295205.1:n.529+136_530-137del
NM_005097.2:c.673+136_674-137del	NP_005088.1:n.673+136_674-137del
NM_005097.3:c.673+136_674-137del	NP_005088.1:n.673+136_674-137del
NR_131777.1:n.937+136_938-137del
XM_017016911.2:c.673+136_674-137del	XP_016872400.1:n.673+136_674-137del
XM_017016912.2:c.529+136_530-137del	XP_016872401.1:n.529+136_530-137del
NM_005097.4:c.673+136_674-137del MANE Select	NP_005088.1:n.673+136_674-137del
NM_001308275.2:c.673+136_674-137del	NP_001295204.1:n.673+136_674-137del
NM_001308276.2:c.529+136_530-137del	NP_001295205.1:n.529+136_530-137del
NR_131777.2:n.810+136_811-137del