Canonical Allele Identifier: CA377627883

Gene: LGI1

Linked Data

• MyVariant Identifiers: chr10:g.95557022A>C (hg19) ; chr10:g.93797265A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93797265A>C , CM000672.2:g.93797265A>C	GRCh38
NC_000010.10:g.95557022A>C , CM000672.1:g.95557022A>C	GRCh37
NC_000010.9:g.95547012A>C	NCBI36
NG_011832.1:g.44457A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371418.9:c.1136A>C MANE Select	ENSP00000360472.4:p.Asp379Ala
ENST00000485458.3:n.5112A>C
ENST00000635804.1:n.570A>C
ENST00000635953.1:c.*558A>C	ENSP00000490058.1:n.*558A>C
ENST00000636155.1:c.838+3915A>C	ENSP00000490355.1:n.838+3915A>C
ENST00000636232.1:c.*922A>C	ENSP00000490325.1:n.*922A>C
ENST00000636754.1:c.*978A>C	ENSP00000489781.1:n.*978A>C
ENST00000636946.1:c.*1008-484A>C	ENSP00000490654.1:n.*1008-484A>C
ENST00000637037.1:c.*726A>C	ENSP00000490860.1:n.*726A>C
ENST00000637347.1:n.997A>C
ENST00000637611.1:c.*692A>C	ENSP00000489682.1:n.*692A>C
ENST00000637689.1:c.-236A>C	ENSP00000490496.1:n.-236A>C
ENST00000637925.1:c.*731A>C	ENSP00000489763.1:n.*731A>C
ENST00000638049.1:c.*894A>C	ENSP00000490597.1:n.*894A>C
ENST00000676175.1:n.2875A>C
ENST00000371413.4:c.839-484A>C	ENSP00000360467.3:n.839-484A>C
ENST00000371418.8:c.1136A>C	ENSP00000360472.4:p.Asp379Ala
ENST00000626307.1:n.5051A>C
ENST00000627420.2:c.*845A>C	ENSP00000487116.1:n.*845A>C
ENST00000629035.2:c.1064A>C	ENSP00000486908.1:p.Asp355Ala
ENST00000630047.2:c.992A>C	ENSP00000485917.1:p.Asp331Ala
NM_001308275.1:c.839-484A>C	NP_001295204.1:n.839-484A>C
NM_001308276.1:c.992A>C	NP_001295205.1:p.Asp331Ala
NM_005097.2:c.1136A>C	NP_005088.1:p.Asp379Ala
NM_005097.3:c.1136A>C	NP_005088.1:p.Asp379Ala
NR_131777.1:n.1400A>C
XM_017016912.2:c.695-484A>C	XP_016872401.1:n.695-484A>C
NM_005097.4:c.1136A>C MANE Select	NP_005088.1:p.Asp379Ala
NM_001308275.2:c.839-484A>C	NP_001295204.1:n.839-484A>C
NM_001308276.2:c.992A>C	NP_001295205.1:p.Asp331Ala
NR_131777.2:n.1273A>C