Canonical Allele Identifier: CA377624570

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553091T>G (hg19) ; chr10:g.93793334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793334T>G , CM000672.2:g.93793334T>G	GRCh38
NC_000010.10:g.95553091T>G , CM000672.1:g.95553091T>G	GRCh37
NC_000010.9:g.95543081T>G	NCBI36
NG_011832.1:g.40526T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.822T>G MANE Select	ENSP00000360472.4:p.Asn274Lys
ENST00000485458.3:n.4798T>G
ENST00000635953.1:c.822T>G	ENSP00000490058.1:p.Asn274Lys
ENST00000636155.1:c.822T>G	ENSP00000490355.1:p.Asn274Lys
ENST00000636232.1:c.*608T>G	ENSP00000490325.1:n.*608T>G
ENST00000636754.1:c.*664T>G	ENSP00000489781.1:n.*664T>G
ENST00000636946.1:c.*991T>G	ENSP00000490654.1:n.*991T>G
ENST00000637037.1:c.*412T>G	ENSP00000490860.1:n.*412T>G
ENST00000637347.1:n.683T>G
ENST00000637611.1:c.*378T>G	ENSP00000489682.1:n.*378T>G
ENST00000637689.1:c.-550T>G	ENSP00000490496.1:n.-550T>G
ENST00000637925.1:c.*417T>G	ENSP00000489763.1:n.*417T>G
ENST00000638049.1:c.*580T>G	ENSP00000490597.1:n.*580T>G
ENST00000676175.1:n.2561T>G
ENST00000371413.4:c.822T>G	ENSP00000360467.3:p.Asn274Lys
ENST00000371418.8:c.822T>G	ENSP00000360472.4:p.Asn274Lys
ENST00000626307.1:n.4737T>G
ENST00000626946.1:n.492T>G
ENST00000627420.2:c.*531T>G	ENSP00000487116.1:n.*531T>G
ENST00000629035.2:c.750T>G	ENSP00000486908.1:p.Asn250Lys
ENST00000630047.2:c.678T>G	ENSP00000485917.1:p.Asn226Lys
ENST00000630487.2:c.*612T>G	ENSP00000486859.1:n.*612T>G
NM_001308275.1:c.822T>G	NP_001295204.1:p.Asn274Lys
NM_001308276.1:c.678T>G	NP_001295205.1:p.Asn226Lys
NM_005097.2:c.822T>G	NP_005088.1:p.Asn274Lys
NM_005097.3:c.822T>G	NP_005088.1:p.Asn274Lys
NR_131777.1:n.1086T>G
XM_017016911.2:c.822T>G	XP_016872400.1:p.Asn274Lys
XM_017016912.2:c.678T>G	XP_016872401.1:p.Asn226Lys
NM_005097.4:c.822T>G MANE Select	NP_005088.1:p.Asn274Lys
NM_001308275.2:c.822T>G	NP_001295204.1:p.Asn274Lys
NM_001308276.2:c.678T>G	NP_001295205.1:p.Asn226Lys
NR_131777.2:n.959T>G