Canonical Allele Identifier: CA377624625

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95553100C>G (hg19) ; chr10:g.93793343C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793343C>G , CM000672.2:g.93793343C>G	GRCh38
NC_000010.10:g.95553100C>G , CM000672.1:g.95553100C>G	GRCh37
NC_000010.9:g.95543090C>G	NCBI36
NG_011832.1:g.40535C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.831C>G MANE Select	ENSP00000360472.4:p.Asn277Lys
ENST00000485458.3:n.4807C>G
ENST00000635953.1:c.831C>G	ENSP00000490058.1:p.Asn277Lys
ENST00000636155.1:c.831C>G	ENSP00000490355.1:p.Asn277Lys
ENST00000636232.1:c.*617C>G	ENSP00000490325.1:n.*617C>G
ENST00000636754.1:c.*673C>G	ENSP00000489781.1:n.*673C>G
ENST00000636946.1:c.*1000C>G	ENSP00000490654.1:n.*1000C>G
ENST00000637037.1:c.*421C>G	ENSP00000490860.1:n.*421C>G
ENST00000637347.1:n.692C>G
ENST00000637611.1:c.*387C>G	ENSP00000489682.1:n.*387C>G
ENST00000637689.1:c.-541C>G	ENSP00000490496.1:n.-541C>G
ENST00000637925.1:c.*426C>G	ENSP00000489763.1:n.*426C>G
ENST00000638049.1:c.*589C>G	ENSP00000490597.1:n.*589C>G
ENST00000676175.1:n.2570C>G
ENST00000371413.4:c.831C>G	ENSP00000360467.3:p.Asn277Lys
ENST00000371418.8:c.831C>G	ENSP00000360472.4:p.Asn277Lys
ENST00000626307.1:n.4746C>G
ENST00000626946.1:n.501C>G
ENST00000627420.2:c.*540C>G	ENSP00000487116.1:n.*540C>G
ENST00000629035.2:c.759C>G	ENSP00000486908.1:p.Asn253Lys
ENST00000630047.2:c.687C>G	ENSP00000485917.1:p.Asn229Lys
ENST00000630487.2:c.*621C>G	ENSP00000486859.1:n.*621C>G
NM_001308275.1:c.831C>G	NP_001295204.1:p.Asn277Lys
NM_001308276.1:c.687C>G	NP_001295205.1:p.Asn229Lys
NM_005097.2:c.831C>G	NP_005088.1:p.Asn277Lys
NM_005097.3:c.831C>G	NP_005088.1:p.Asn277Lys
NR_131777.1:n.1095C>G
XM_017016911.2:c.831C>G	XP_016872400.1:p.Asn277Lys
XM_017016912.2:c.687C>G	XP_016872401.1:p.Asn229Lys
NM_005097.4:c.831C>G MANE Select	NP_005088.1:p.Asn277Lys
NM_001308275.2:c.831C>G	NP_001295204.1:p.Asn277Lys
NM_001308276.2:c.687C>G	NP_001295205.1:p.Asn229Lys
NR_131777.2:n.968C>G