Canonical Allele Identifier: CA470800071

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552950A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793193A>T , CM000672.2:g.93793193A>T	GRCh38
NC_000010.10:g.95552950A>T , CM000672.1:g.95552950A>T	GRCh37
NC_000010.9:g.95542940A>T	NCBI36
NG_011832.1:g.40385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.681A>T MANE Select	ENSP00000360472.4:p.Ala227=
ENST00000485458.3:n.4657A>T
ENST00000635953.1:c.681A>T	ENSP00000490058.1:p.Ala227=
ENST00000636155.1:c.681A>T	ENSP00000490355.1:p.Ala227=
ENST00000636232.1:c.*467A>T	ENSP00000490325.1:n.*467A>T
ENST00000636754.1:c.*523A>T	ENSP00000489781.1:n.*523A>T
ENST00000636946.1:c.*850A>T	ENSP00000490654.1:n.*850A>T
ENST00000637037.1:c.*271A>T	ENSP00000490860.1:n.*271A>T
ENST00000637347.1:n.542A>T
ENST00000637611.1:c.*237A>T	ENSP00000489682.1:n.*237A>T
ENST00000637689.1:c.-691A>T	ENSP00000490496.1:n.-691A>T
ENST00000637925.1:c.*276A>T	ENSP00000489763.1:n.*276A>T
ENST00000638049.1:c.*439A>T	ENSP00000490597.1:n.*439A>T
ENST00000676175.1:n.2420A>T
ENST00000371413.4:c.681A>T	ENSP00000360467.3:p.Ala227=
ENST00000371418.8:c.681A>T	ENSP00000360472.4:p.Ala227=
ENST00000626307.1:n.4596A>T
ENST00000626946.1:n.351A>T
ENST00000627420.2:c.*390A>T	ENSP00000487116.1:n.*390A>T
ENST00000629035.2:c.609A>T	ENSP00000486908.1:p.Ala203=
ENST00000630047.2:c.537A>T	ENSP00000485917.1:p.Ala179=
ENST00000630412.1:n.469A>T
ENST00000630487.2:c.*471A>T	ENSP00000486859.1:n.*471A>T
NM_001308275.1:c.681A>T	NP_001295204.1:p.Ala227=
NM_001308276.1:c.537A>T	NP_001295205.1:p.Ala179=
NM_005097.2:c.681A>T	NP_005088.1:p.Ala227=
NM_005097.3:c.681A>T	NP_005088.1:p.Ala227=
NR_131777.1:n.945A>T
XM_017016911.2:c.681A>T	XP_016872400.1:p.Ala227=
XM_017016912.2:c.537A>T	XP_016872401.1:p.Ala179=
NM_005097.4:c.681A>T MANE Select	NP_005088.1:p.Ala227=
NM_001308275.2:c.681A>T	NP_001295204.1:p.Ala227=
NM_001308276.2:c.537A>T	NP_001295205.1:p.Ala179=
NR_131777.2:n.818A>T