Canonical Allele Identifier: CA377624632

Gene: LGI1

Linked Data

• gnomAD v4: 10-93793344-A-G
• MyVariant Identifiers: chr10:g.95553101A>G (hg19) ; chr10:g.93793344A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793344A>G , CM000672.2:g.93793344A>G	GRCh38
NC_000010.10:g.95553101A>G , CM000672.1:g.95553101A>G	GRCh37
NC_000010.9:g.95543091A>G	NCBI36
NG_011832.1:g.40536A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.832A>G MANE Select	ENSP00000360472.4:p.Ile278Val
ENST00000485458.3:n.4808A>G
ENST00000635953.1:c.832A>G	ENSP00000490058.1:p.Ile278Val
ENST00000636155.1:c.832A>G	ENSP00000490355.1:p.Ile278Val
ENST00000636232.1:c.*618A>G	ENSP00000490325.1:n.*618A>G
ENST00000636754.1:c.*674A>G	ENSP00000489781.1:n.*674A>G
ENST00000636946.1:c.*1001A>G	ENSP00000490654.1:n.*1001A>G
ENST00000637037.1:c.*422A>G	ENSP00000490860.1:n.*422A>G
ENST00000637347.1:n.693A>G
ENST00000637611.1:c.*388A>G	ENSP00000489682.1:n.*388A>G
ENST00000637689.1:c.-540A>G	ENSP00000490496.1:n.-540A>G
ENST00000637925.1:c.*427A>G	ENSP00000489763.1:n.*427A>G
ENST00000638049.1:c.*590A>G	ENSP00000490597.1:n.*590A>G
ENST00000676175.1:n.2571A>G
ENST00000371413.4:c.832A>G	ENSP00000360467.3:p.Ile278Val
ENST00000371418.8:c.832A>G	ENSP00000360472.4:p.Ile278Val
ENST00000626307.1:n.4747A>G
ENST00000626946.1:n.502A>G
ENST00000627420.2:c.*541A>G	ENSP00000487116.1:n.*541A>G
ENST00000629035.2:c.760A>G	ENSP00000486908.1:p.Ile254Val
ENST00000630047.2:c.688A>G	ENSP00000485917.1:p.Ile230Val
ENST00000630487.2:c.*622A>G	ENSP00000486859.1:n.*622A>G
NM_001308275.1:c.832A>G	NP_001295204.1:p.Ile278Val
NM_001308276.1:c.688A>G	NP_001295205.1:p.Ile230Val
NM_005097.2:c.832A>G	NP_005088.1:p.Ile278Val
NM_005097.3:c.832A>G	NP_005088.1:p.Ile278Val
NR_131777.1:n.1096A>G
XM_017016911.2:c.832A>G	XP_016872400.1:p.Ile278Val
XM_017016912.2:c.688A>G	XP_016872401.1:p.Ile230Val
NM_005097.4:c.832A>G MANE Select	NP_005088.1:p.Ile278Val
NM_001308275.2:c.832A>G	NP_001295204.1:p.Ile278Val
NM_001308276.2:c.688A>G	NP_001295205.1:p.Ile230Val
NR_131777.2:n.969A>G