Canonical Allele Identifier: CA377624584

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553093A>G (hg19) ; chr10:g.93793336A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793336A>G , CM000672.2:g.93793336A>G	GRCh38
NC_000010.10:g.95553093A>G , CM000672.1:g.95553093A>G	GRCh37
NC_000010.9:g.95543083A>G	NCBI36
NG_011832.1:g.40528A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.824A>G MANE Select	ENSP00000360472.4:p.Tyr275Cys
ENST00000485458.3:n.4800A>G
ENST00000635953.1:c.824A>G	ENSP00000490058.1:p.Tyr275Cys
ENST00000636155.1:c.824A>G	ENSP00000490355.1:p.Tyr275Cys
ENST00000636232.1:c.*610A>G	ENSP00000490325.1:n.*610A>G
ENST00000636754.1:c.*666A>G	ENSP00000489781.1:n.*666A>G
ENST00000636946.1:c.*993A>G	ENSP00000490654.1:n.*993A>G
ENST00000637037.1:c.*414A>G	ENSP00000490860.1:n.*414A>G
ENST00000637347.1:n.685A>G
ENST00000637611.1:c.*380A>G	ENSP00000489682.1:n.*380A>G
ENST00000637689.1:c.-548A>G	ENSP00000490496.1:n.-548A>G
ENST00000637925.1:c.*419A>G	ENSP00000489763.1:n.*419A>G
ENST00000638049.1:c.*582A>G	ENSP00000490597.1:n.*582A>G
ENST00000676175.1:n.2563A>G
ENST00000371413.4:c.824A>G	ENSP00000360467.3:p.Tyr275Cys
ENST00000371418.8:c.824A>G	ENSP00000360472.4:p.Tyr275Cys
ENST00000626307.1:n.4739A>G
ENST00000626946.1:n.494A>G
ENST00000627420.2:c.*533A>G	ENSP00000487116.1:n.*533A>G
ENST00000629035.2:c.752A>G	ENSP00000486908.1:p.Tyr251Cys
ENST00000630047.2:c.680A>G	ENSP00000485917.1:p.Tyr227Cys
ENST00000630487.2:c.*614A>G	ENSP00000486859.1:n.*614A>G
NM_001308275.1:c.824A>G	NP_001295204.1:p.Tyr275Cys
NM_001308276.1:c.680A>G	NP_001295205.1:p.Tyr227Cys
NM_005097.2:c.824A>G	NP_005088.1:p.Tyr275Cys
NM_005097.3:c.824A>G	NP_005088.1:p.Tyr275Cys
NR_131777.1:n.1088A>G
XM_017016911.2:c.824A>G	XP_016872400.1:p.Tyr275Cys
XM_017016912.2:c.680A>G	XP_016872401.1:p.Tyr227Cys
NM_005097.4:c.824A>G MANE Select	NP_005088.1:p.Tyr275Cys
NM_001308275.2:c.824A>G	NP_001295204.1:p.Tyr275Cys
NM_001308276.2:c.680A>G	NP_001295205.1:p.Tyr227Cys
NR_131777.2:n.961A>G