Canonical Allele Identifier: CA377627204

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556919T>G (hg19) ; chr10:g.93797162T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797162T>G , CM000672.2:g.93797162T>G	GRCh38
NC_000010.10:g.95556919T>G , CM000672.1:g.95556919T>G	GRCh37
NC_000010.9:g.95546909T>G	NCBI36
NG_011832.1:g.44354T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1033T>G MANE Select	ENSP00000360472.4:p.Tyr345Asp
ENST00000485458.3:n.5009T>G
ENST00000635804.1:n.467T>G
ENST00000635953.1:c.*455T>G	ENSP00000490058.1:n.*455T>G
ENST00000636155.1:c.838+3812T>G	ENSP00000490355.1:n.838+3812T>G
ENST00000636232.1:c.*819T>G	ENSP00000490325.1:n.*819T>G
ENST00000636754.1:c.*875T>G	ENSP00000489781.1:n.*875T>G
ENST00000636946.1:c.*1008-587T>G	ENSP00000490654.1:n.*1008-587T>G
ENST00000637037.1:c.*623T>G	ENSP00000490860.1:n.*623T>G
ENST00000637347.1:n.894T>G
ENST00000637611.1:c.*589T>G	ENSP00000489682.1:n.*589T>G
ENST00000637689.1:c.-339T>G	ENSP00000490496.1:n.-339T>G
ENST00000637925.1:c.*628T>G	ENSP00000489763.1:n.*628T>G
ENST00000638049.1:c.*791T>G	ENSP00000490597.1:n.*791T>G
ENST00000676175.1:n.2772T>G
ENST00000371413.4:c.839-587T>G	ENSP00000360467.3:n.839-587T>G
ENST00000371418.8:c.1033T>G	ENSP00000360472.4:p.Tyr345Asp
ENST00000626307.1:n.4948T>G
ENST00000627420.2:c.*742T>G	ENSP00000487116.1:n.*742T>G
ENST00000629035.2:c.961T>G	ENSP00000486908.1:p.Tyr321Asp
ENST00000630047.2:c.889T>G	ENSP00000485917.1:p.Tyr297Asp
NM_001308275.1:c.839-587T>G	NP_001295204.1:n.839-587T>G
NM_001308276.1:c.889T>G	NP_001295205.1:p.Tyr297Asp
NM_005097.2:c.1033T>G	NP_005088.1:p.Tyr345Asp
NM_005097.3:c.1033T>G	NP_005088.1:p.Tyr345Asp
NR_131777.1:n.1297T>G
XM_017016912.2:c.695-587T>G	XP_016872401.1:n.695-587T>G
NM_005097.4:c.1033T>G MANE Select	NP_005088.1:p.Tyr345Asp
NM_001308275.2:c.839-587T>G	NP_001295204.1:n.839-587T>G
NM_001308276.2:c.889T>G	NP_001295205.1:p.Tyr297Asp
NR_131777.2:n.1170T>G