Canonical Allele Identifier: CA2610226349

Gene: LGI1

Linked Data

• gnomAD v4: 10-93792944-AATTAAAATAAGGGCTACCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93792945_93792963del , CM000672.2:g.93792945_93792963del	GRCh38
NC_000010.10:g.95552702_95552720del , CM000672.1:g.95552702_95552720del	GRCh37
NC_000010.9:g.95542692_95542710del	NCBI36
NG_011832.1:g.40137_40155del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.673+33_673+51del MANE Select	ENSP00000360472.4:n.673+33_673+51del
ENST00000485458.3:n.4649+33_4649+51del
ENST00000635953.1:c.673+33_673+51del	ENSP00000490058.1:n.673+33_673+51del
ENST00000636155.1:c.673+33_673+51del	ENSP00000490355.1:n.673+33_673+51del
ENST00000636232.1:c.*459+33_*459+51del	ENSP00000490325.1:n.*459+33_*459+51del
ENST00000636754.1:c.*515+33_*515+51del	ENSP00000489781.1:n.*515+33_*515+51del
ENST00000636946.1:c.*842+33_*842+51del	ENSP00000490654.1:n.*842+33_*842+51del
ENST00000637037.1:c.*263+33_*263+51del	ENSP00000490860.1:n.*263+33_*263+51del
ENST00000637347.1:n.534+33_534+51del
ENST00000637611.1:c.*229+33_*229+51del	ENSP00000489682.1:n.*229+33_*229+51del
ENST00000637689.1:c.-699+33_-699+51del	ENSP00000490496.1:n.-699+33_-699+51del
ENST00000637925.1:c.*268+33_*268+51del	ENSP00000489763.1:n.*268+33_*268+51del
ENST00000638049.1:c.*431+33_*431+51del	ENSP00000490597.1:n.*431+33_*431+51del
ENST00000676175.1:n.2412+33_2412+51del
ENST00000371413.4:c.673+33_673+51del	ENSP00000360467.3:n.673+33_673+51del
ENST00000371418.8:c.673+33_673+51del	ENSP00000360472.4:n.673+33_673+51del
ENST00000626307.1:n.4588+33_4588+51del
ENST00000626946.1:n.103_121del
ENST00000627420.2:c.*382+33_*382+51del	ENSP00000487116.1:n.*382+33_*382+51del
ENST00000629035.2:c.601+33_601+51del	ENSP00000486908.1:n.601+33_601+51del
ENST00000630047.2:c.529+33_529+51del	ENSP00000485917.1:n.529+33_529+51del
ENST00000630412.1:n.461+33_461+51del
ENST00000630487.2:c.*463+33_*463+51del	ENSP00000486859.1:n.*463+33_*463+51del
NM_001308275.1:c.673+33_673+51del	NP_001295204.1:n.673+33_673+51del
NM_001308276.1:c.529+33_529+51del	NP_001295205.1:n.529+33_529+51del
NM_005097.2:c.673+33_673+51del	NP_005088.1:n.673+33_673+51del
NM_005097.3:c.673+33_673+51del	NP_005088.1:n.673+33_673+51del
NR_131777.1:n.937+33_937+51del
XM_017016911.2:c.673+33_673+51del	XP_016872400.1:n.673+33_673+51del
XM_017016912.2:c.529+33_529+51del	XP_016872401.1:n.529+33_529+51del
NM_005097.4:c.673+33_673+51del MANE Select	NP_005088.1:n.673+33_673+51del
NM_001308275.2:c.673+33_673+51del	NP_001295204.1:n.673+33_673+51del
NM_001308276.2:c.529+33_529+51del	NP_001295205.1:n.529+33_529+51del
NR_131777.2:n.810+33_810+51del