Canonical Allele Identifier: CA377627842

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557015T>G (hg19) ; chr10:g.93797258T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797258T>G , CM000672.2:g.93797258T>G	GRCh38
NC_000010.10:g.95557015T>G , CM000672.1:g.95557015T>G	GRCh37
NC_000010.9:g.95547005T>G	NCBI36
NG_011832.1:g.44450T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1129T>G MANE Select	ENSP00000360472.4:p.Tyr377Asp
ENST00000485458.3:n.5105T>G
ENST00000635804.1:n.563T>G
ENST00000635953.1:c.*551T>G	ENSP00000490058.1:n.*551T>G
ENST00000636155.1:c.838+3908T>G	ENSP00000490355.1:n.838+3908T>G
ENST00000636232.1:c.*915T>G	ENSP00000490325.1:n.*915T>G
ENST00000636754.1:c.*971T>G	ENSP00000489781.1:n.*971T>G
ENST00000636946.1:c.*1008-491T>G	ENSP00000490654.1:n.*1008-491T>G
ENST00000637037.1:c.*719T>G	ENSP00000490860.1:n.*719T>G
ENST00000637347.1:n.990T>G
ENST00000637611.1:c.*685T>G	ENSP00000489682.1:n.*685T>G
ENST00000637689.1:c.-243T>G	ENSP00000490496.1:n.-243T>G
ENST00000637925.1:c.*724T>G	ENSP00000489763.1:n.*724T>G
ENST00000638049.1:c.*887T>G	ENSP00000490597.1:n.*887T>G
ENST00000676175.1:n.2868T>G
ENST00000371413.4:c.839-491T>G	ENSP00000360467.3:n.839-491T>G
ENST00000371418.8:c.1129T>G	ENSP00000360472.4:p.Tyr377Asp
ENST00000626307.1:n.5044T>G
ENST00000627420.2:c.*838T>G	ENSP00000487116.1:n.*838T>G
ENST00000629035.2:c.1057T>G	ENSP00000486908.1:p.Tyr353Asp
ENST00000630047.2:c.985T>G	ENSP00000485917.1:p.Tyr329Asp
NM_001308275.1:c.839-491T>G	NP_001295204.1:n.839-491T>G
NM_001308276.1:c.985T>G	NP_001295205.1:p.Tyr329Asp
NM_005097.2:c.1129T>G	NP_005088.1:p.Tyr377Asp
NM_005097.3:c.1129T>G	NP_005088.1:p.Tyr377Asp
NR_131777.1:n.1393T>G
XM_017016912.2:c.695-491T>G	XP_016872401.1:n.695-491T>G
NM_005097.4:c.1129T>G MANE Select	NP_005088.1:p.Tyr377Asp
NM_001308275.2:c.839-491T>G	NP_001295204.1:n.839-491T>G
NM_001308276.2:c.985T>G	NP_001295205.1:p.Tyr329Asp
NR_131777.2:n.1266T>G