Canonical Allele Identifier: CA10636537

Gene: LGI1

Linked Data

• ClinVar Variation Id: 301652
• ClinVar RCV Id: RCV000401284
• dbSNP Id: rs150194814
• gnomAD v2: 10-95517675-T-C
• gnomAD v3: 10-93757918-T-C
• gnomAD v4: 10-93757918-T-C
• MyVariant Identifiers: chr10:g.95517675T>C (hg19) ; chr10:g.93757918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.93757918T>C , CM000672.2:g.93757918T>C	GRCh38
NC_000010.10:g.95517675T>C , CM000672.1:g.95517675T>C	GRCh37
NC_000010.9:g.95507665T>C	NCBI36
NG_011832.1:g.5110T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371418.8:c.-227T>C	ENSP00000360472.4:n.-227T>C
ENST00000478763.2:c.-227T>C	ENSP00000486517.1:n.-227T>C
ENST00000627420.2:c.-227T>C	ENSP00000487116.1:n.-227T>C
ENST00000629035.2:c.-227T>C	ENSP00000486908.1:n.-227T>C
ENST00000630487.2:c.-227T>C	ENSP00000486859.1:n.-227T>C
NM_001308275.1:c.-227T>C	NP_001295204.1:n.-227T>C
NM_001308276.1:c.-227T>C	NP_001295205.1:n.-227T>C
NM_005097.2:c.-227T>C	NP_005088.1:n.-227T>C
NM_005097.3:c.-227T>C	NP_005088.1:n.-227T>C
NR_131777.1:n.110T>C
XM_017016911.2:c.-227T>C	XP_016872400.1:n.-227T>C
XM_017016912.2:c.-227T>C	XP_016872401.1:n.-227T>C