Canonical Allele Identifier: CA377626702

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95556844A>G (hg19) ; chr10:g.93797087A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797087A>G , CM000672.2:g.93797087A>G	GRCh38
NC_000010.10:g.95556844A>G , CM000672.1:g.95556844A>G	GRCh37
NC_000010.9:g.95546834A>G	NCBI36
NG_011832.1:g.44279A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.958A>G MANE Select	ENSP00000360472.4:p.Lys320Glu
ENST00000485458.3:n.4934A>G
ENST00000635804.1:n.392A>G
ENST00000635953.1:c.*380A>G	ENSP00000490058.1:n.*380A>G
ENST00000636155.1:c.838+3737A>G	ENSP00000490355.1:n.838+3737A>G
ENST00000636232.1:c.*744A>G	ENSP00000490325.1:n.*744A>G
ENST00000636754.1:c.*800A>G	ENSP00000489781.1:n.*800A>G
ENST00000636946.1:c.*1008-662A>G	ENSP00000490654.1:n.*1008-662A>G
ENST00000637037.1:c.*548A>G	ENSP00000490860.1:n.*548A>G
ENST00000637347.1:n.819A>G
ENST00000637611.1:c.*514A>G	ENSP00000489682.1:n.*514A>G
ENST00000637689.1:c.-414A>G	ENSP00000490496.1:n.-414A>G
ENST00000637925.1:c.*553A>G	ENSP00000489763.1:n.*553A>G
ENST00000638049.1:c.*716A>G	ENSP00000490597.1:n.*716A>G
ENST00000676175.1:n.2697A>G
ENST00000371413.4:c.839-662A>G	ENSP00000360467.3:n.839-662A>G
ENST00000371418.8:c.958A>G	ENSP00000360472.4:p.Lys320Glu
ENST00000626307.1:n.4873A>G
ENST00000627420.2:c.*667A>G	ENSP00000487116.1:n.*667A>G
ENST00000629035.2:c.886A>G	ENSP00000486908.1:p.Lys296Glu
ENST00000630047.2:c.814A>G	ENSP00000485917.1:p.Lys272Glu
NM_001308275.1:c.839-662A>G	NP_001295204.1:n.839-662A>G
NM_001308276.1:c.814A>G	NP_001295205.1:p.Lys272Glu
NM_005097.2:c.958A>G	NP_005088.1:p.Lys320Glu
NM_005097.3:c.958A>G	NP_005088.1:p.Lys320Glu
NR_131777.1:n.1222A>G
XM_017016912.2:c.695-662A>G	XP_016872401.1:n.695-662A>G
NM_005097.4:c.958A>G MANE Select	NP_005088.1:p.Lys320Glu
NM_001308275.2:c.839-662A>G	NP_001295204.1:n.839-662A>G
NM_001308276.2:c.814A>G	NP_001295205.1:p.Lys272Glu
NR_131777.2:n.1095A>G