Canonical Allele Identifier: CA470800068

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552947T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793190T>C , CM000672.2:g.93793190T>C	GRCh38
NC_000010.10:g.95552947T>C , CM000672.1:g.95552947T>C	GRCh37
NC_000010.9:g.95542937T>C	NCBI36
NG_011832.1:g.40382T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.678T>C MANE Select	ENSP00000360472.4:p.Phe226=
ENST00000485458.3:n.4654T>C
ENST00000635953.1:c.678T>C	ENSP00000490058.1:p.Phe226=
ENST00000636155.1:c.678T>C	ENSP00000490355.1:p.Phe226=
ENST00000636232.1:c.*464T>C	ENSP00000490325.1:n.*464T>C
ENST00000636754.1:c.*520T>C	ENSP00000489781.1:n.*520T>C
ENST00000636946.1:c.*847T>C	ENSP00000490654.1:n.*847T>C
ENST00000637037.1:c.*268T>C	ENSP00000490860.1:n.*268T>C
ENST00000637347.1:n.539T>C
ENST00000637611.1:c.*234T>C	ENSP00000489682.1:n.*234T>C
ENST00000637689.1:c.-694T>C	ENSP00000490496.1:n.-694T>C
ENST00000637925.1:c.*273T>C	ENSP00000489763.1:n.*273T>C
ENST00000638049.1:c.*436T>C	ENSP00000490597.1:n.*436T>C
ENST00000676175.1:n.2417T>C
ENST00000371413.4:c.678T>C	ENSP00000360467.3:p.Phe226=
ENST00000371418.8:c.678T>C	ENSP00000360472.4:p.Phe226=
ENST00000626307.1:n.4593T>C
ENST00000626946.1:n.348T>C
ENST00000627420.2:c.*387T>C	ENSP00000487116.1:n.*387T>C
ENST00000629035.2:c.606T>C	ENSP00000486908.1:p.Phe202=
ENST00000630047.2:c.534T>C	ENSP00000485917.1:p.Phe178=
ENST00000630412.1:n.466T>C
ENST00000630487.2:c.*468T>C	ENSP00000486859.1:n.*468T>C
NM_001308275.1:c.678T>C	NP_001295204.1:p.Phe226=
NM_001308276.1:c.534T>C	NP_001295205.1:p.Phe178=
NM_005097.2:c.678T>C	NP_005088.1:p.Phe226=
NM_005097.3:c.678T>C	NP_005088.1:p.Phe226=
NR_131777.1:n.942T>C
XM_017016911.2:c.678T>C	XP_016872400.1:p.Phe226=
XM_017016912.2:c.534T>C	XP_016872401.1:p.Phe178=
NM_005097.4:c.678T>C MANE Select	NP_005088.1:p.Phe226=
NM_001308275.2:c.678T>C	NP_001295204.1:p.Phe226=
NM_001308276.2:c.534T>C	NP_001295205.1:p.Phe178=
NR_131777.2:n.815T>C