Canonical Allele Identifier: CA377627223

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556922T>G (hg19) ; chr10:g.93797165T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797165T>G , CM000672.2:g.93797165T>G	GRCh38
NC_000010.10:g.95556922T>G , CM000672.1:g.95556922T>G	GRCh37
NC_000010.9:g.95546912T>G	NCBI36
NG_011832.1:g.44357T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1036T>G MANE Select	ENSP00000360472.4:p.Phe346Val
ENST00000485458.3:n.5012T>G
ENST00000635804.1:n.470T>G
ENST00000635953.1:c.*458T>G	ENSP00000490058.1:n.*458T>G
ENST00000636155.1:c.838+3815T>G	ENSP00000490355.1:n.838+3815T>G
ENST00000636232.1:c.*822T>G	ENSP00000490325.1:n.*822T>G
ENST00000636754.1:c.*878T>G	ENSP00000489781.1:n.*878T>G
ENST00000636946.1:c.*1008-584T>G	ENSP00000490654.1:n.*1008-584T>G
ENST00000637037.1:c.*626T>G	ENSP00000490860.1:n.*626T>G
ENST00000637347.1:n.897T>G
ENST00000637611.1:c.*592T>G	ENSP00000489682.1:n.*592T>G
ENST00000637689.1:c.-336T>G	ENSP00000490496.1:n.-336T>G
ENST00000637925.1:c.*631T>G	ENSP00000489763.1:n.*631T>G
ENST00000638049.1:c.*794T>G	ENSP00000490597.1:n.*794T>G
ENST00000676175.1:n.2775T>G
ENST00000371413.4:c.839-584T>G	ENSP00000360467.3:n.839-584T>G
ENST00000371418.8:c.1036T>G	ENSP00000360472.4:p.Phe346Val
ENST00000626307.1:n.4951T>G
ENST00000627420.2:c.*745T>G	ENSP00000487116.1:n.*745T>G
ENST00000629035.2:c.964T>G	ENSP00000486908.1:p.Phe322Val
ENST00000630047.2:c.892T>G	ENSP00000485917.1:p.Phe298Val
NM_001308275.1:c.839-584T>G	NP_001295204.1:n.839-584T>G
NM_001308276.1:c.892T>G	NP_001295205.1:p.Phe298Val
NM_005097.2:c.1036T>G	NP_005088.1:p.Phe346Val
NM_005097.3:c.1036T>G	NP_005088.1:p.Phe346Val
NR_131777.1:n.1300T>G
XM_017016912.2:c.695-584T>G	XP_016872401.1:n.695-584T>G
NM_005097.4:c.1036T>G MANE Select	NP_005088.1:p.Phe346Val
NM_001308275.2:c.839-584T>G	NP_001295204.1:n.839-584T>G
NM_001308276.2:c.892T>G	NP_001295205.1:p.Phe298Val
NR_131777.2:n.1173T>G