Canonical Allele Identifier: CA377627914

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557028A>G (hg19) ; chr10:g.93797271A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797271A>G , CM000672.2:g.93797271A>G	GRCh38
NC_000010.10:g.95557028A>G , CM000672.1:g.95557028A>G	GRCh37
NC_000010.9:g.95547018A>G	NCBI36
NG_011832.1:g.44463A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1142A>G MANE Select	ENSP00000360472.4:p.Asp381Gly
ENST00000485458.3:n.5118A>G
ENST00000635804.1:n.576A>G
ENST00000635953.1:c.*564A>G	ENSP00000490058.1:n.*564A>G
ENST00000636155.1:c.838+3921A>G	ENSP00000490355.1:n.838+3921A>G
ENST00000636232.1:c.*928A>G	ENSP00000490325.1:n.*928A>G
ENST00000636754.1:c.*984A>G	ENSP00000489781.1:n.*984A>G
ENST00000636946.1:c.*1008-478A>G	ENSP00000490654.1:n.*1008-478A>G
ENST00000637037.1:c.*732A>G	ENSP00000490860.1:n.*732A>G
ENST00000637347.1:n.1003A>G
ENST00000637611.1:c.*698A>G	ENSP00000489682.1:n.*698A>G
ENST00000637689.1:c.-230A>G	ENSP00000490496.1:n.-230A>G
ENST00000637925.1:c.*737A>G	ENSP00000489763.1:n.*737A>G
ENST00000638049.1:c.*900A>G	ENSP00000490597.1:n.*900A>G
ENST00000676175.1:n.2881A>G
ENST00000371413.4:c.839-478A>G	ENSP00000360467.3:n.839-478A>G
ENST00000371418.8:c.1142A>G	ENSP00000360472.4:p.Asp381Gly
ENST00000626307.1:n.5057A>G
ENST00000627420.2:c.*851A>G	ENSP00000487116.1:n.*851A>G
ENST00000629035.2:c.1070A>G	ENSP00000486908.1:p.Asp357Gly
ENST00000630047.2:c.998A>G	ENSP00000485917.1:p.Asp333Gly
NM_001308275.1:c.839-478A>G	NP_001295204.1:n.839-478A>G
NM_001308276.1:c.998A>G	NP_001295205.1:p.Asp333Gly
NM_005097.2:c.1142A>G	NP_005088.1:p.Asp381Gly
NM_005097.3:c.1142A>G	NP_005088.1:p.Asp381Gly
NR_131777.1:n.1406A>G
XM_017016912.2:c.695-478A>G	XP_016872401.1:n.695-478A>G
NM_005097.4:c.1142A>G MANE Select	NP_005088.1:p.Asp381Gly
NM_001308275.2:c.839-478A>G	NP_001295204.1:n.839-478A>G
NM_001308276.2:c.998A>G	NP_001295205.1:p.Asp333Gly
NR_131777.2:n.1279A>G