Canonical Allele Identifier: CA377623959

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95552963C>G (hg19) ; chr10:g.93793206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93793206C>G , CM000672.2:g.93793206C>G	GRCh38
NC_000010.10:g.95552963C>G , CM000672.1:g.95552963C>G	GRCh37
NC_000010.9:g.95542953C>G	NCBI36
NG_011832.1:g.40398C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.694C>G MANE Select	ENSP00000360472.4:p.Leu232Val
ENST00000485458.3:n.4670C>G
ENST00000635953.1:c.694C>G	ENSP00000490058.1:p.Leu232Val
ENST00000636155.1:c.694C>G	ENSP00000490355.1:p.Leu232Val
ENST00000636232.1:c.*480C>G	ENSP00000490325.1:n.*480C>G
ENST00000636754.1:c.*536C>G	ENSP00000489781.1:n.*536C>G
ENST00000636946.1:c.*863C>G	ENSP00000490654.1:n.*863C>G
ENST00000637037.1:c.*284C>G	ENSP00000490860.1:n.*284C>G
ENST00000637347.1:n.555C>G
ENST00000637611.1:c.*250C>G	ENSP00000489682.1:n.*250C>G
ENST00000637689.1:c.-678C>G	ENSP00000490496.1:n.-678C>G
ENST00000637925.1:c.*289C>G	ENSP00000489763.1:n.*289C>G
ENST00000638049.1:c.*452C>G	ENSP00000490597.1:n.*452C>G
ENST00000676175.1:n.2433C>G
ENST00000371413.4:c.694C>G	ENSP00000360467.3:p.Leu232Val
ENST00000371418.8:c.694C>G	ENSP00000360472.4:p.Leu232Val
ENST00000626307.1:n.4609C>G
ENST00000626946.1:n.364C>G
ENST00000627420.2:c.*403C>G	ENSP00000487116.1:n.*403C>G
ENST00000629035.2:c.622C>G	ENSP00000486908.1:p.Leu208Val
ENST00000630047.2:c.550C>G	ENSP00000485917.1:p.Leu184Val
ENST00000630412.1:n.482C>G
ENST00000630487.2:c.*484C>G	ENSP00000486859.1:n.*484C>G
NM_001308275.1:c.694C>G	NP_001295204.1:p.Leu232Val
NM_001308276.1:c.550C>G	NP_001295205.1:p.Leu184Val
NM_005097.2:c.694C>G	NP_005088.1:p.Leu232Val
NM_005097.3:c.694C>G	NP_005088.1:p.Leu232Val
NR_131777.1:n.958C>G
XM_017016911.2:c.694C>G	XP_016872400.1:p.Leu232Val
XM_017016912.2:c.550C>G	XP_016872401.1:p.Leu184Val
NM_005097.4:c.694C>G MANE Select	NP_005088.1:p.Leu232Val
NM_001308275.2:c.694C>G	NP_001295204.1:p.Leu232Val
NM_001308276.2:c.550C>G	NP_001295205.1:p.Leu184Val
NR_131777.2:n.831C>G