Canonical Allele Identifier: CA377632212

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95518567T>C (hg19) ; chr10:g.93758810T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758810T>C , CM000672.2:g.93758810T>C	GRCh38
NC_000010.10:g.95518567T>C , CM000672.1:g.95518567T>C	GRCh37
NC_000010.9:g.95508557T>C	NCBI36
NG_011832.1:g.6002T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.266T>C MANE Select	ENSP00000360472.4:p.Phe89Ser
ENST00000635953.1:c.266T>C	ENSP00000490058.1:p.Phe89Ser
ENST00000636140.1:n.51T>C
ENST00000636155.1:c.266T>C	ENSP00000490355.1:p.Phe89Ser
ENST00000636232.1:c.*52T>C	ENSP00000490325.1:n.*52T>C
ENST00000636683.1:n.21T>C
ENST00000636754.1:c.*56T>C	ENSP00000489781.1:n.*56T>C
ENST00000636946.1:c.266T>C	ENSP00000490654.1:p.Phe89Ser
ENST00000637037.1:c.266T>C	ENSP00000490860.1:p.Phe89Ser
ENST00000637347.1:n.148+122T>C
ENST00000637611.1:c.266T>C	ENSP00000489682.1:p.Phe89Ser
ENST00000637689.1:c.-1106T>C	ENSP00000490496.1:n.-1106T>C
ENST00000637925.1:c.266T>C	ENSP00000489763.1:p.Phe89Ser
ENST00000638049.1:c.*24T>C	ENSP00000490597.1:n.*24T>C
ENST00000371413.4:c.266T>C	ENSP00000360467.3:p.Phe89Ser
ENST00000371418.8:c.266T>C	ENSP00000360472.4:p.Phe89Ser
ENST00000478763.2:c.266T>C	ENSP00000486517.1:p.Phe89Ser
ENST00000627420.2:c.*56T>C	ENSP00000487116.1:n.*56T>C
ENST00000627699.1:c.*56T>C	ENSP00000485868.1:n.*56T>C
ENST00000629035.2:c.215+451T>C	ENSP00000486908.1:n.215+451T>C
ENST00000630047.2:c.266T>C	ENSP00000485917.1:p.Phe89Ser
ENST00000630184.2:c.266T>C	ENSP00000486607.1:p.Phe89Ser
ENST00000630487.2:c.*56T>C	ENSP00000486859.1:n.*56T>C
NM_001308275.1:c.266T>C	NP_001295204.1:p.Phe89Ser
NM_001308276.1:c.266T>C	NP_001295205.1:p.Phe89Ser
NM_005097.2:c.266T>C	NP_005088.1:p.Phe89Ser
NM_005097.3:c.266T>C	NP_005088.1:p.Phe89Ser
NR_131777.1:n.611T>C
XM_017016911.2:c.266T>C	XP_016872400.1:p.Phe89Ser
XM_017016912.2:c.266T>C	XP_016872401.1:p.Phe89Ser
NM_005097.4:c.266T>C MANE Select	NP_005088.1:p.Phe89Ser
NM_001308275.2:c.266T>C	NP_001295204.1:p.Phe89Ser
NM_001308276.2:c.266T>C	NP_001295205.1:p.Phe89Ser
NR_131777.2:n.484T>C