Canonical Allele Identifier: CA16621545
Gene: LGI4 HGNC NCBI

Linked Data

ClinVar Variation Id: 424867
ClinVar RCV Id: RCV000487486
dbSNP Id: rs1064797093

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35126848C>G , CM000681.2:g.35126848C>G GRCh38
NC_000019.9:g.35617752C>G , CM000681.1:g.35617752C>G GRCh37
NC_000019.8:g.40309592C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310123.8:c.793+5G>C MANE Select ENSP00000312273.3:n.793+5G>C
ENST00000310123.7:c.793+5G>C ENSP00000312273.3:n.793+5G>C
ENST00000392225.7:c.798G>C ENSP00000376059.3:p.Glu266Asp
ENST00000493050.5:n.852+5G>C
ENST00000587780.5:c.528+5G>C
ENST00000591840.5:n.420-1982G>C
ENST00000593248.5:n.929G>C
NM_139284.2:c.793+5G>C NP_644813.1:n.793+5G>C
XM_011526594.1:c.793+5G>C XP_011524896.1:n.793+5G>C
XM_011526595.1:c.277+5G>C XP_011524897.1:n.277+5G>C
XM_011526595.2:c.277+5G>C XP_011524897.1:n.277+5G>C
XM_017026428.1:c.277+5G>C XP_016881917.1:n.277+5G>C
XM_017026429.1:c.277+5G>C XP_016881918.1:n.277+5G>C
XM_017026430.2:c.277+5G>C XP_016881919.1:n.277+5G>C
NM_139284.3:c.793+5G>C MANE Select NP_644813.1:n.793+5G>C