Canonical Allele Identifier: CA377623920

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552954T>A (hg19) ; chr10:g.93793197T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793197T>A , CM000672.2:g.93793197T>A	GRCh38
NC_000010.10:g.95552954T>A , CM000672.1:g.95552954T>A	GRCh37
NC_000010.9:g.95542944T>A	NCBI36
NG_011832.1:g.40389T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.685T>A MANE Select	ENSP00000360472.4:p.Ser229Thr
ENST00000485458.3:n.4661T>A
ENST00000635953.1:c.685T>A	ENSP00000490058.1:p.Ser229Thr
ENST00000636155.1:c.685T>A	ENSP00000490355.1:p.Ser229Thr
ENST00000636232.1:c.*471T>A	ENSP00000490325.1:n.*471T>A
ENST00000636754.1:c.*527T>A	ENSP00000489781.1:n.*527T>A
ENST00000636946.1:c.*854T>A	ENSP00000490654.1:n.*854T>A
ENST00000637037.1:c.*275T>A	ENSP00000490860.1:n.*275T>A
ENST00000637347.1:n.546T>A
ENST00000637611.1:c.*241T>A	ENSP00000489682.1:n.*241T>A
ENST00000637689.1:c.-687T>A	ENSP00000490496.1:n.-687T>A
ENST00000637925.1:c.*280T>A	ENSP00000489763.1:n.*280T>A
ENST00000638049.1:c.*443T>A	ENSP00000490597.1:n.*443T>A
ENST00000676175.1:n.2424T>A
ENST00000371413.4:c.685T>A	ENSP00000360467.3:p.Ser229Thr
ENST00000371418.8:c.685T>A	ENSP00000360472.4:p.Ser229Thr
ENST00000626307.1:n.4600T>A
ENST00000626946.1:n.355T>A
ENST00000627420.2:c.*394T>A	ENSP00000487116.1:n.*394T>A
ENST00000629035.2:c.613T>A	ENSP00000486908.1:p.Ser205Thr
ENST00000630047.2:c.541T>A	ENSP00000485917.1:p.Ser181Thr
ENST00000630412.1:n.473T>A
ENST00000630487.2:c.*475T>A	ENSP00000486859.1:n.*475T>A
NM_001308275.1:c.685T>A	NP_001295204.1:p.Ser229Thr
NM_001308276.1:c.541T>A	NP_001295205.1:p.Ser181Thr
NM_005097.2:c.685T>A	NP_005088.1:p.Ser229Thr
NM_005097.3:c.685T>A	NP_005088.1:p.Ser229Thr
NR_131777.1:n.949T>A
XM_017016911.2:c.685T>A	XP_016872400.1:p.Ser229Thr
XM_017016912.2:c.541T>A	XP_016872401.1:p.Ser181Thr
NM_005097.4:c.685T>A MANE Select	NP_005088.1:p.Ser229Thr
NM_001308275.2:c.685T>A	NP_001295204.1:p.Ser229Thr
NM_001308276.2:c.541T>A	NP_001295205.1:p.Ser181Thr
NR_131777.2:n.822T>A