Canonical Allele Identifier: CA2610226459

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793024-ATTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793025_93793028del , CM000672.2:g.93793025_93793028del	GRCh38
NC_000010.10:g.95552782_95552785del , CM000672.1:g.95552782_95552785del	GRCh37
NC_000010.9:g.95542772_95542775del	NCBI36
NG_011832.1:g.40217_40220del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.673+113_673+116del MANE Select	ENSP00000360472.4:n.673+113_673+116del
ENST00000485458.3:n.4649+113_4649+116del
ENST00000635953.1:c.673+113_673+116del	ENSP00000490058.1:n.673+113_673+116del
ENST00000636155.1:c.673+113_673+116del	ENSP00000490355.1:n.673+113_673+116del
ENST00000636232.1:c.*459+113_*459+116del	ENSP00000490325.1:n.*459+113_*459+116del
ENST00000636754.1:c.*515+113_*515+116del	ENSP00000489781.1:n.*515+113_*515+116del
ENST00000636946.1:c.*842+113_*842+116del	ENSP00000490654.1:n.*842+113_*842+116del
ENST00000637037.1:c.*263+113_*263+116del	ENSP00000490860.1:n.*263+113_*263+116del
ENST00000637347.1:n.534+113_534+116del
ENST00000637611.1:c.*229+113_*229+116del	ENSP00000489682.1:n.*229+113_*229+116del
ENST00000637689.1:c.-699+113_-699+116del	ENSP00000490496.1:n.-699+113_-699+116del
ENST00000637925.1:c.*268+113_*268+116del	ENSP00000489763.1:n.*268+113_*268+116del
ENST00000638049.1:c.*431+113_*431+116del	ENSP00000490597.1:n.*431+113_*431+116del
ENST00000676175.1:n.2412+113_2412+116del
ENST00000371413.4:c.673+113_673+116del	ENSP00000360467.3:n.673+113_673+116del
ENST00000371418.8:c.673+113_673+116del	ENSP00000360472.4:n.673+113_673+116del
ENST00000626307.1:n.4588+113_4588+116del
ENST00000626946.1:n.183_186del
ENST00000627420.2:c.*382+113_*382+116del	ENSP00000487116.1:n.*382+113_*382+116del
ENST00000629035.2:c.601+113_601+116del	ENSP00000486908.1:n.601+113_601+116del
ENST00000630047.2:c.529+113_529+116del	ENSP00000485917.1:n.529+113_529+116del
ENST00000630412.1:n.461+113_461+116del
ENST00000630487.2:c.*463+113_*463+116del	ENSP00000486859.1:n.*463+113_*463+116del
NM_001308275.1:c.673+113_673+116del	NP_001295204.1:n.673+113_673+116del
NM_001308276.1:c.529+113_529+116del	NP_001295205.1:n.529+113_529+116del
NM_005097.2:c.673+113_673+116del	NP_005088.1:n.673+113_673+116del
NM_005097.3:c.673+113_673+116del	NP_005088.1:n.673+113_673+116del
NR_131777.1:n.937+113_937+116del
XM_017016911.2:c.673+113_673+116del	XP_016872400.1:n.673+113_673+116del
XM_017016912.2:c.529+113_529+116del	XP_016872401.1:n.529+113_529+116del
NM_005097.4:c.673+113_673+116del MANE Select	NP_005088.1:n.673+113_673+116del
NM_001308275.2:c.673+113_673+116del	NP_001295204.1:n.673+113_673+116del
NM_001308276.2:c.529+113_529+116del	NP_001295205.1:n.529+113_529+116del
NR_131777.2:n.810+113_810+116del