Canonical Allele Identifier: CA377627155

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556914A>T (hg19) ; chr10:g.93797157A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797157A>T , CM000672.2:g.93797157A>T	GRCh38
NC_000010.10:g.95556914A>T , CM000672.1:g.95556914A>T	GRCh37
NC_000010.9:g.95546904A>T	NCBI36
NG_011832.1:g.44349A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1028A>T MANE Select	ENSP00000360472.4:p.Asn343Ile
ENST00000485458.3:n.5004A>T
ENST00000635804.1:n.462A>T
ENST00000635953.1:c.*450A>T	ENSP00000490058.1:n.*450A>T
ENST00000636155.1:c.838+3807A>T	ENSP00000490355.1:n.838+3807A>T
ENST00000636232.1:c.*814A>T	ENSP00000490325.1:n.*814A>T
ENST00000636754.1:c.*870A>T	ENSP00000489781.1:n.*870A>T
ENST00000636946.1:c.*1008-592A>T	ENSP00000490654.1:n.*1008-592A>T
ENST00000637037.1:c.*618A>T	ENSP00000490860.1:n.*618A>T
ENST00000637347.1:n.889A>T
ENST00000637611.1:c.*584A>T	ENSP00000489682.1:n.*584A>T
ENST00000637689.1:c.-344A>T	ENSP00000490496.1:n.-344A>T
ENST00000637925.1:c.*623A>T	ENSP00000489763.1:n.*623A>T
ENST00000638049.1:c.*786A>T	ENSP00000490597.1:n.*786A>T
ENST00000676175.1:n.2767A>T
ENST00000371413.4:c.839-592A>T	ENSP00000360467.3:n.839-592A>T
ENST00000371418.8:c.1028A>T	ENSP00000360472.4:p.Asn343Ile
ENST00000626307.1:n.4943A>T
ENST00000627420.2:c.*737A>T	ENSP00000487116.1:n.*737A>T
ENST00000629035.2:c.956A>T	ENSP00000486908.1:p.Asn319Ile
ENST00000630047.2:c.884A>T	ENSP00000485917.1:p.Asn295Ile
NM_001308275.1:c.839-592A>T	NP_001295204.1:n.839-592A>T
NM_001308276.1:c.884A>T	NP_001295205.1:p.Asn295Ile
NM_005097.2:c.1028A>T	NP_005088.1:p.Asn343Ile
NM_005097.3:c.1028A>T	NP_005088.1:p.Asn343Ile
NR_131777.1:n.1292A>T
XM_017016912.2:c.695-592A>T	XP_016872401.1:n.695-592A>T
NM_005097.4:c.1028A>T MANE Select	NP_005088.1:p.Asn343Ile
NM_001308275.2:c.839-592A>T	NP_001295204.1:n.839-592A>T
NM_001308276.2:c.884A>T	NP_001295205.1:p.Asn295Ile
NR_131777.2:n.1165A>T