Canonical Allele Identifier: CA377623951

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552961A>T (hg19) ; chr10:g.93793204A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793204A>T , CM000672.2:g.93793204A>T	GRCh38
NC_000010.10:g.95552961A>T , CM000672.1:g.95552961A>T	GRCh37
NC_000010.9:g.95542951A>T	NCBI36
NG_011832.1:g.40396A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.692A>T MANE Select	ENSP00000360472.4:p.Asp231Val
ENST00000485458.3:n.4668A>T
ENST00000635953.1:c.692A>T	ENSP00000490058.1:p.Asp231Val
ENST00000636155.1:c.692A>T	ENSP00000490355.1:p.Asp231Val
ENST00000636232.1:c.*478A>T	ENSP00000490325.1:n.*478A>T
ENST00000636754.1:c.*534A>T	ENSP00000489781.1:n.*534A>T
ENST00000636946.1:c.*861A>T	ENSP00000490654.1:n.*861A>T
ENST00000637037.1:c.*282A>T	ENSP00000490860.1:n.*282A>T
ENST00000637347.1:n.553A>T
ENST00000637611.1:c.*248A>T	ENSP00000489682.1:n.*248A>T
ENST00000637689.1:c.-680A>T	ENSP00000490496.1:n.-680A>T
ENST00000637925.1:c.*287A>T	ENSP00000489763.1:n.*287A>T
ENST00000638049.1:c.*450A>T	ENSP00000490597.1:n.*450A>T
ENST00000676175.1:n.2431A>T
ENST00000371413.4:c.692A>T	ENSP00000360467.3:p.Asp231Val
ENST00000371418.8:c.692A>T	ENSP00000360472.4:p.Asp231Val
ENST00000626307.1:n.4607A>T
ENST00000626946.1:n.362A>T
ENST00000627420.2:c.*401A>T	ENSP00000487116.1:n.*401A>T
ENST00000629035.2:c.620A>T	ENSP00000486908.1:p.Asp207Val
ENST00000630047.2:c.548A>T	ENSP00000485917.1:p.Asp183Val
ENST00000630412.1:n.480A>T
ENST00000630487.2:c.*482A>T	ENSP00000486859.1:n.*482A>T
NM_001308275.1:c.692A>T	NP_001295204.1:p.Asp231Val
NM_001308276.1:c.548A>T	NP_001295205.1:p.Asp183Val
NM_005097.2:c.692A>T	NP_005088.1:p.Asp231Val
NM_005097.3:c.692A>T	NP_005088.1:p.Asp231Val
NR_131777.1:n.956A>T
XM_017016911.2:c.692A>T	XP_016872400.1:p.Asp231Val
XM_017016912.2:c.548A>T	XP_016872401.1:p.Asp183Val
NM_005097.4:c.692A>T MANE Select	NP_005088.1:p.Asp231Val
NM_001308275.2:c.692A>T	NP_001295204.1:p.Asp231Val
NM_001308276.2:c.548A>T	NP_001295205.1:p.Asp183Val
NR_131777.2:n.829A>T