Canonical Allele Identifier: CA470800087

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552977A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793220A>G , CM000672.2:g.93793220A>G	GRCh38
NC_000010.10:g.95552977A>G , CM000672.1:g.95552977A>G	GRCh37
NC_000010.9:g.95542967A>G	NCBI36
NG_011832.1:g.40412A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.708A>G MANE Select	ENSP00000360472.4:p.Ser236=
ENST00000485458.3:n.4684A>G
ENST00000635953.1:c.708A>G	ENSP00000490058.1:p.Ser236=
ENST00000636155.1:c.708A>G	ENSP00000490355.1:p.Ser236=
ENST00000636232.1:c.*494A>G	ENSP00000490325.1:n.*494A>G
ENST00000636754.1:c.*550A>G	ENSP00000489781.1:n.*550A>G
ENST00000636946.1:c.*877A>G	ENSP00000490654.1:n.*877A>G
ENST00000637037.1:c.*298A>G	ENSP00000490860.1:n.*298A>G
ENST00000637347.1:n.569A>G
ENST00000637611.1:c.*264A>G	ENSP00000489682.1:n.*264A>G
ENST00000637689.1:c.-664A>G	ENSP00000490496.1:n.-664A>G
ENST00000637925.1:c.*303A>G	ENSP00000489763.1:n.*303A>G
ENST00000638049.1:c.*466A>G	ENSP00000490597.1:n.*466A>G
ENST00000676175.1:n.2447A>G
ENST00000371413.4:c.708A>G	ENSP00000360467.3:p.Ser236=
ENST00000371418.8:c.708A>G	ENSP00000360472.4:p.Ser236=
ENST00000626307.1:n.4623A>G
ENST00000626946.1:n.378A>G
ENST00000627420.2:c.*417A>G	ENSP00000487116.1:n.*417A>G
ENST00000629035.2:c.636A>G	ENSP00000486908.1:p.Ser212=
ENST00000630047.2:c.564A>G	ENSP00000485917.1:p.Ser188=
ENST00000630412.1:n.496A>G
ENST00000630487.2:c.*498A>G	ENSP00000486859.1:n.*498A>G
NM_001308275.1:c.708A>G	NP_001295204.1:p.Ser236=
NM_001308276.1:c.564A>G	NP_001295205.1:p.Ser188=
NM_005097.2:c.708A>G	NP_005088.1:p.Ser236=
NM_005097.3:c.708A>G	NP_005088.1:p.Ser236=
NR_131777.1:n.972A>G
XM_017016911.2:c.708A>G	XP_016872400.1:p.Ser236=
XM_017016912.2:c.564A>G	XP_016872401.1:p.Ser188=
NM_005097.4:c.708A>G MANE Select	NP_005088.1:p.Ser236=
NM_001308275.2:c.708A>G	NP_001295204.1:p.Ser236=
NM_001308276.2:c.564A>G	NP_001295205.1:p.Ser188=
NR_131777.2:n.845A>G