Canonical Allele Identifier: CA377626751

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556852G>T (hg19) ; chr10:g.93797095G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797095G>T , CM000672.2:g.93797095G>T	GRCh38
NC_000010.10:g.95556852G>T , CM000672.1:g.95556852G>T	GRCh37
NC_000010.9:g.95546842G>T	NCBI36
NG_011832.1:g.44287G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.966G>T MANE Select	ENSP00000360472.4:p.Gln322His
ENST00000485458.3:n.4942G>T
ENST00000635804.1:n.400G>T
ENST00000635953.1:c.*388G>T	ENSP00000490058.1:n.*388G>T
ENST00000636155.1:c.838+3745G>T	ENSP00000490355.1:n.838+3745G>T
ENST00000636232.1:c.*752G>T	ENSP00000490325.1:n.*752G>T
ENST00000636754.1:c.*808G>T	ENSP00000489781.1:n.*808G>T
ENST00000636946.1:c.*1008-654G>T	ENSP00000490654.1:n.*1008-654G>T
ENST00000637037.1:c.*556G>T	ENSP00000490860.1:n.*556G>T
ENST00000637347.1:n.827G>T
ENST00000637611.1:c.*522G>T	ENSP00000489682.1:n.*522G>T
ENST00000637689.1:c.-406G>T	ENSP00000490496.1:n.-406G>T
ENST00000637925.1:c.*561G>T	ENSP00000489763.1:n.*561G>T
ENST00000638049.1:c.*724G>T	ENSP00000490597.1:n.*724G>T
ENST00000676175.1:n.2705G>T
ENST00000371413.4:c.839-654G>T	ENSP00000360467.3:n.839-654G>T
ENST00000371418.8:c.966G>T	ENSP00000360472.4:p.Gln322His
ENST00000626307.1:n.4881G>T
ENST00000627420.2:c.*675G>T	ENSP00000487116.1:n.*675G>T
ENST00000629035.2:c.894G>T	ENSP00000486908.1:p.Gln298His
ENST00000630047.2:c.822G>T	ENSP00000485917.1:p.Gln274His
NM_001308275.1:c.839-654G>T	NP_001295204.1:n.839-654G>T
NM_001308276.1:c.822G>T	NP_001295205.1:p.Gln274His
NM_005097.2:c.966G>T	NP_005088.1:p.Gln322His
NM_005097.3:c.966G>T	NP_005088.1:p.Gln322His
NR_131777.1:n.1230G>T
XM_017016912.2:c.695-654G>T	XP_016872401.1:n.695-654G>T
NM_005097.4:c.966G>T MANE Select	NP_005088.1:p.Gln322His
NM_001308275.2:c.839-654G>T	NP_001295204.1:n.839-654G>T
NM_001308276.2:c.822G>T	NP_001295205.1:p.Gln274His
NR_131777.2:n.1103G>T