Canonical Allele Identifier: CA377624078

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552988A>T (hg19) ; chr10:g.93793231A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793231A>T , CM000672.2:g.93793231A>T	GRCh38
NC_000010.10:g.95552988A>T , CM000672.1:g.95552988A>T	GRCh37
NC_000010.9:g.95542978A>T	NCBI36
NG_011832.1:g.40423A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.719A>T MANE Select	ENSP00000360472.4:p.Asp240Val
ENST00000485458.3:n.4695A>T
ENST00000635953.1:c.719A>T	ENSP00000490058.1:p.Asp240Val
ENST00000636155.1:c.719A>T	ENSP00000490355.1:p.Asp240Val
ENST00000636232.1:c.*505A>T	ENSP00000490325.1:n.*505A>T
ENST00000636754.1:c.*561A>T	ENSP00000489781.1:n.*561A>T
ENST00000636946.1:c.*888A>T	ENSP00000490654.1:n.*888A>T
ENST00000637037.1:c.*309A>T	ENSP00000490860.1:n.*309A>T
ENST00000637347.1:n.580A>T
ENST00000637611.1:c.*275A>T	ENSP00000489682.1:n.*275A>T
ENST00000637689.1:c.-653A>T	ENSP00000490496.1:n.-653A>T
ENST00000637925.1:c.*314A>T	ENSP00000489763.1:n.*314A>T
ENST00000638049.1:c.*477A>T	ENSP00000490597.1:n.*477A>T
ENST00000676175.1:n.2458A>T
ENST00000371413.4:c.719A>T	ENSP00000360467.3:p.Asp240Val
ENST00000371418.8:c.719A>T	ENSP00000360472.4:p.Asp240Val
ENST00000626307.1:n.4634A>T
ENST00000626946.1:n.389A>T
ENST00000627420.2:c.*428A>T	ENSP00000487116.1:n.*428A>T
ENST00000629035.2:c.647A>T	ENSP00000486908.1:p.Asp216Val
ENST00000630047.2:c.575A>T	ENSP00000485917.1:p.Asp192Val
ENST00000630412.1:n.507A>T
ENST00000630487.2:c.*509A>T	ENSP00000486859.1:n.*509A>T
NM_001308275.1:c.719A>T	NP_001295204.1:p.Asp240Val
NM_001308276.1:c.575A>T	NP_001295205.1:p.Asp192Val
NM_005097.2:c.719A>T	NP_005088.1:p.Asp240Val
NM_005097.3:c.719A>T	NP_005088.1:p.Asp240Val
NR_131777.1:n.983A>T
XM_017016911.2:c.719A>T	XP_016872400.1:p.Asp240Val
XM_017016912.2:c.575A>T	XP_016872401.1:p.Asp192Val
NM_005097.4:c.719A>T MANE Select	NP_005088.1:p.Asp240Val
NM_001308275.2:c.719A>T	NP_001295204.1:p.Asp240Val
NM_001308276.2:c.575A>T	NP_001295205.1:p.Asp192Val
NR_131777.2:n.856A>T