Canonical Allele Identifier: CA2574616799

Gene: LGI1

Linked Data

• gnomAD v4: 10-93758893-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758893T>A , CM000672.2:g.93758893T>A	GRCh38
NC_000010.10:g.95518650T>A , CM000672.1:g.95518650T>A	GRCh37
NC_000010.9:g.95508640T>A	NCBI36
NG_011832.1:g.6085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+62T>A MANE Select	ENSP00000360472.4:n.287+62T>A
ENST00000635953.1:c.287+62T>A	ENSP00000490058.1:n.287+62T>A
ENST00000636140.1:n.72+62T>A
ENST00000636155.1:c.287+62T>A	ENSP00000490355.1:n.287+62T>A
ENST00000636232.1:c.*73+62T>A	ENSP00000490325.1:n.*73+62T>A
ENST00000636683.1:n.42+62T>A
ENST00000636754.1:c.*77+62T>A	ENSP00000489781.1:n.*77+62T>A
ENST00000636946.1:c.*58T>A	ENSP00000490654.1:n.*58T>A
ENST00000637037.1:c.287+62T>A	ENSP00000490860.1:n.287+62T>A
ENST00000637347.1:n.148+205T>A
ENST00000637611.1:c.287+62T>A	ENSP00000489682.1:n.287+62T>A
ENST00000637689.1:c.-1085+62T>A	ENSP00000490496.1:n.-1085+62T>A
ENST00000637925.1:c.287+62T>A	ENSP00000489763.1:n.287+62T>A
ENST00000638049.1:c.*45+62T>A	ENSP00000490597.1:n.*45+62T>A
ENST00000371413.4:c.287+62T>A	ENSP00000360467.3:n.287+62T>A
ENST00000371418.8:c.287+62T>A	ENSP00000360472.4:n.287+62T>A
ENST00000478763.2:c.*58T>A	ENSP00000486517.1:n.*58T>A
ENST00000627420.2:c.*77+62T>A	ENSP00000487116.1:n.*77+62T>A
ENST00000627699.1:c.*139T>A	ENSP00000485868.1:n.*139T>A
ENST00000629035.2:c.215+534T>A	ENSP00000486908.1:n.215+534T>A
ENST00000630047.2:c.287+62T>A	ENSP00000485917.1:n.287+62T>A
ENST00000630184.2:c.287+62T>A	ENSP00000486607.1:n.287+62T>A
ENST00000630487.2:c.*77+62T>A	ENSP00000486859.1:n.*77+62T>A
NM_001308275.1:c.287+62T>A	NP_001295204.1:n.287+62T>A
NM_001308276.1:c.287+62T>A	NP_001295205.1:n.287+62T>A
NM_005097.2:c.287+62T>A	NP_005088.1:n.287+62T>A
NM_005097.3:c.287+62T>A	NP_005088.1:n.287+62T>A
NR_131777.1:n.632+62T>A
XM_017016911.2:c.287+62T>A	XP_016872400.1:n.287+62T>A
XM_017016912.2:c.287+62T>A	XP_016872401.1:n.287+62T>A
XR_001747552.1:n.4982A>T
XR_002957095.1:n.7110A>T
XR_002957096.1:n.8322A>T
NM_005097.4:c.287+62T>A MANE Select	NP_005088.1:n.287+62T>A
NM_001308275.2:c.287+62T>A	NP_001295204.1:n.287+62T>A
NM_001308276.2:c.287+62T>A	NP_001295205.1:n.287+62T>A
NR_131777.2:n.505+62T>A