Canonical Allele Identifier: CA377627864

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557018A>T (hg19) ; chr10:g.93797261A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797261A>T , CM000672.2:g.93797261A>T	GRCh38
NC_000010.10:g.95557018A>T , CM000672.1:g.95557018A>T	GRCh37
NC_000010.9:g.95547008A>T	NCBI36
NG_011832.1:g.44453A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1132A>T MANE Select	ENSP00000360472.4:p.Arg378Trp
ENST00000485458.3:n.5108A>T
ENST00000635804.1:n.566A>T
ENST00000635953.1:c.*554A>T	ENSP00000490058.1:n.*554A>T
ENST00000636155.1:c.838+3911A>T	ENSP00000490355.1:n.838+3911A>T
ENST00000636232.1:c.*918A>T	ENSP00000490325.1:n.*918A>T
ENST00000636754.1:c.*974A>T	ENSP00000489781.1:n.*974A>T
ENST00000636946.1:c.*1008-488A>T	ENSP00000490654.1:n.*1008-488A>T
ENST00000637037.1:c.*722A>T	ENSP00000490860.1:n.*722A>T
ENST00000637347.1:n.993A>T
ENST00000637611.1:c.*688A>T	ENSP00000489682.1:n.*688A>T
ENST00000637689.1:c.-240A>T	ENSP00000490496.1:n.-240A>T
ENST00000637925.1:c.*727A>T	ENSP00000489763.1:n.*727A>T
ENST00000638049.1:c.*890A>T	ENSP00000490597.1:n.*890A>T
ENST00000676175.1:n.2871A>T
ENST00000371413.4:c.839-488A>T	ENSP00000360467.3:n.839-488A>T
ENST00000371418.8:c.1132A>T	ENSP00000360472.4:p.Arg378Trp
ENST00000626307.1:n.5047A>T
ENST00000627420.2:c.*841A>T	ENSP00000487116.1:n.*841A>T
ENST00000629035.2:c.1060A>T	ENSP00000486908.1:p.Arg354Trp
ENST00000630047.2:c.988A>T	ENSP00000485917.1:p.Arg330Trp
NM_001308275.1:c.839-488A>T	NP_001295204.1:n.839-488A>T
NM_001308276.1:c.988A>T	NP_001295205.1:p.Arg330Trp
NM_005097.2:c.1132A>T	NP_005088.1:p.Arg378Trp
NM_005097.3:c.1132A>T	NP_005088.1:p.Arg378Trp
NR_131777.1:n.1396A>T
XM_017016912.2:c.695-488A>T	XP_016872401.1:n.695-488A>T
NM_005097.4:c.1132A>T MANE Select	NP_005088.1:p.Arg378Trp
NM_001308275.2:c.839-488A>T	NP_001295204.1:n.839-488A>T
NM_001308276.2:c.988A>T	NP_001295205.1:p.Arg330Trp
NR_131777.2:n.1269A>T