Canonical Allele Identifier: CA377632298

Gene: LGI1

Linked Data

• ClinVar Variation Id: 2626760
• ClinVar RCV Id: RCV003384292
• MyVariant Identifiers: chr10:g.95518591G>C (hg19) ; chr10:g.93758834G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93758834G>C , CM000672.2:g.93758834G>C	GRCh38
NC_000010.10:g.95518591G>C , CM000672.1:g.95518591G>C	GRCh37
NC_000010.9:g.95508581G>C	NCBI36
NG_011832.1:g.6026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.9:c.287+3G>C MANE Select	ENSP00000360472.4:n.287+3G>C
ENST00000635953.1:c.287+3G>C	ENSP00000490058.1:n.287+3G>C
ENST00000636140.1:n.72+3G>C
ENST00000636155.1:c.287+3G>C	ENSP00000490355.1:n.287+3G>C
ENST00000636232.1:c.*73+3G>C	ENSP00000490325.1:n.*73+3G>C
ENST00000636683.1:n.42+3G>C
ENST00000636754.1:c.*77+3G>C	ENSP00000489781.1:n.*77+3G>C
ENST00000636946.1:c.290G>C	ENSP00000490654.1:p.Ter97Ser
ENST00000637037.1:c.287+3G>C	ENSP00000490860.1:n.287+3G>C
ENST00000637347.1:n.148+146G>C
ENST00000637611.1:c.287+3G>C	ENSP00000489682.1:n.287+3G>C
ENST00000637689.1:c.-1085+3G>C	ENSP00000490496.1:n.-1085+3G>C
ENST00000637925.1:c.287+3G>C	ENSP00000489763.1:n.287+3G>C
ENST00000638049.1:c.*45+3G>C	ENSP00000490597.1:n.*45+3G>C
ENST00000371413.4:c.287+3G>C	ENSP00000360467.3:n.287+3G>C
ENST00000371418.8:c.287+3G>C	ENSP00000360472.4:n.287+3G>C
ENST00000478763.2:c.290G>C	ENSP00000486517.1:p.Ter97Ser
ENST00000627420.2:c.*77+3G>C	ENSP00000487116.1:n.*77+3G>C
ENST00000627699.1:c.*80G>C	ENSP00000485868.1:n.*80G>C
ENST00000629035.2:c.215+475G>C	ENSP00000486908.1:n.215+475G>C
ENST00000630047.2:c.287+3G>C	ENSP00000485917.1:n.287+3G>C
ENST00000630184.2:c.287+3G>C	ENSP00000486607.1:n.287+3G>C
ENST00000630487.2:c.*77+3G>C	ENSP00000486859.1:n.*77+3G>C
NM_001308275.1:c.287+3G>C	NP_001295204.1:n.287+3G>C
NM_001308276.1:c.287+3G>C	NP_001295205.1:n.287+3G>C
NM_005097.2:c.287+3G>C	NP_005088.1:n.287+3G>C
NM_005097.3:c.287+3G>C	NP_005088.1:n.287+3G>C
NR_131777.1:n.632+3G>C
XM_017016911.2:c.287+3G>C	XP_016872400.1:n.287+3G>C
XM_017016912.2:c.287+3G>C	XP_016872401.1:n.287+3G>C
NM_005097.4:c.287+3G>C MANE Select	NP_005088.1:n.287+3G>C
NM_001308275.2:c.287+3G>C	NP_001295204.1:n.287+3G>C
NM_001308276.2:c.287+3G>C	NP_001295205.1:n.287+3G>C
NR_131777.2:n.505+3G>C