Canonical Allele Identifier: CA470800077

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552962C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793205C>T , CM000672.2:g.93793205C>T	GRCh38
NC_000010.10:g.95552962C>T , CM000672.1:g.95552962C>T	GRCh37
NC_000010.9:g.95542952C>T	NCBI36
NG_011832.1:g.40397C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.693C>T MANE Select	ENSP00000360472.4:p.Asp231=
ENST00000485458.3:n.4669C>T
ENST00000635953.1:c.693C>T	ENSP00000490058.1:p.Asp231=
ENST00000636155.1:c.693C>T	ENSP00000490355.1:p.Asp231=
ENST00000636232.1:c.*479C>T	ENSP00000490325.1:n.*479C>T
ENST00000636754.1:c.*535C>T	ENSP00000489781.1:n.*535C>T
ENST00000636946.1:c.*862C>T	ENSP00000490654.1:n.*862C>T
ENST00000637037.1:c.*283C>T	ENSP00000490860.1:n.*283C>T
ENST00000637347.1:n.554C>T
ENST00000637611.1:c.*249C>T	ENSP00000489682.1:n.*249C>T
ENST00000637689.1:c.-679C>T	ENSP00000490496.1:n.-679C>T
ENST00000637925.1:c.*288C>T	ENSP00000489763.1:n.*288C>T
ENST00000638049.1:c.*451C>T	ENSP00000490597.1:n.*451C>T
ENST00000676175.1:n.2432C>T
ENST00000371413.4:c.693C>T	ENSP00000360467.3:p.Asp231=
ENST00000371418.8:c.693C>T	ENSP00000360472.4:p.Asp231=
ENST00000626307.1:n.4608C>T
ENST00000626946.1:n.363C>T
ENST00000627420.2:c.*402C>T	ENSP00000487116.1:n.*402C>T
ENST00000629035.2:c.621C>T	ENSP00000486908.1:p.Asp207=
ENST00000630047.2:c.549C>T	ENSP00000485917.1:p.Asp183=
ENST00000630412.1:n.481C>T
ENST00000630487.2:c.*483C>T	ENSP00000486859.1:n.*483C>T
NM_001308275.1:c.693C>T	NP_001295204.1:p.Asp231=
NM_001308276.1:c.549C>T	NP_001295205.1:p.Asp183=
NM_005097.2:c.693C>T	NP_005088.1:p.Asp231=
NM_005097.3:c.693C>T	NP_005088.1:p.Asp231=
NR_131777.1:n.957C>T
XM_017016911.2:c.693C>T	XP_016872400.1:p.Asp231=
XM_017016912.2:c.549C>T	XP_016872401.1:p.Asp183=
NM_005097.4:c.693C>T MANE Select	NP_005088.1:p.Asp231=
NM_001308275.2:c.693C>T	NP_001295204.1:p.Asp231=
NM_001308276.2:c.549C>T	NP_001295205.1:p.Asp183=
NR_131777.2:n.830C>T