Canonical Allele Identifier: CA377631979

Gene: LGI1

Linked Data

• gnomAD v4: 10-93758771-G-T
• MyVariant Identifiers: chr10:g.95518528G>T (hg19) ; chr10:g.93758771G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758771G>T , CM000672.2:g.93758771G>T	GRCh38
NC_000010.10:g.95518528G>T , CM000672.1:g.95518528G>T	GRCh37
NC_000010.9:g.95508518G>T	NCBI36
NG_011832.1:g.5963G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.227G>T MANE Select	ENSP00000360472.4:p.Arg76Ile
ENST00000635953.1:c.227G>T	ENSP00000490058.1:p.Arg76Ile
ENST00000636140.1:n.12G>T
ENST00000636155.1:c.227G>T	ENSP00000490355.1:p.Arg76Ile
ENST00000636232.1:c.*13G>T	ENSP00000490325.1:n.*13G>T
ENST00000636754.1:c.*17G>T	ENSP00000489781.1:n.*17G>T
ENST00000636946.1:c.227G>T	ENSP00000490654.1:p.Arg76Ile
ENST00000637037.1:c.227G>T	ENSP00000490860.1:p.Arg76Ile
ENST00000637347.1:n.148+83G>T
ENST00000637611.1:c.227G>T	ENSP00000489682.1:p.Arg76Ile
ENST00000637689.1:c.-1145G>T	ENSP00000490496.1:n.-1145G>T
ENST00000637925.1:c.227G>T	ENSP00000489763.1:p.Arg76Ile
ENST00000638049.1:c.144G>T	ENSP00000490597.1:p.Glu48Asp
ENST00000371413.4:c.227G>T	ENSP00000360467.3:p.Arg76Ile
ENST00000371418.8:c.227G>T	ENSP00000360472.4:p.Arg76Ile
ENST00000478763.2:c.227G>T	ENSP00000486517.1:p.Arg76Ile
ENST00000627420.2:c.*17G>T	ENSP00000487116.1:n.*17G>T
ENST00000627699.1:c.*17G>T	ENSP00000485868.1:n.*17G>T
ENST00000629035.2:c.215+412G>T	ENSP00000486908.1:n.215+412G>T
ENST00000630047.2:c.227G>T	ENSP00000485917.1:p.Arg76Ile
ENST00000630184.2:c.227G>T	ENSP00000486607.1:p.Arg76Ile
ENST00000630487.2:c.*17G>T	ENSP00000486859.1:n.*17G>T
NM_001308275.1:c.227G>T	NP_001295204.1:p.Arg76Ile
NM_001308276.1:c.227G>T	NP_001295205.1:p.Arg76Ile
NM_005097.2:c.227G>T	NP_005088.1:p.Arg76Ile
NM_005097.3:c.227G>T	NP_005088.1:p.Arg76Ile
NR_131777.1:n.572G>T
XM_017016911.2:c.227G>T	XP_016872400.1:p.Arg76Ile
XM_017016912.2:c.227G>T	XP_016872401.1:p.Arg76Ile
NM_005097.4:c.227G>T MANE Select	NP_005088.1:p.Arg76Ile
NM_001308275.2:c.227G>T	NP_001295204.1:p.Arg76Ile
NM_001308276.2:c.227G>T	NP_001295205.1:p.Arg76Ile
NR_131777.2:n.445G>T