Canonical Allele Identifier: CA995435838

Gene: LGI4

Linked Data

• dbSNP Id: rs2065143107
• gnomAD v3: 19-35126868-CG-C
• gnomAD v4: 19-35126868-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126871del , CM000681.2:g.35126871del	GRCh38
NC_000019.9:g.35617775del , CM000681.1:g.35617775del	GRCh37
NC_000019.8:g.40309615del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.777del MANE Select	ENSP00000312273.3:p.Glu260ArgfsTer?
ENST00000310123.7:c.777del	ENSP00000312273.3:p.Glu260ArgfsTer?
ENST00000392225.7:c.777del	ENSP00000376059.3:p.Glu260ArgfsTer23
ENST00000493050.5:n.836del
ENST00000587780.5:c.512del
ENST00000591840.5:n.420-2003del
ENST00000593248.5:n.908del
NM_139284.2:c.777del	NP_644813.1:p.Glu260ArgfsTer?
XM_011526594.1:c.777del	XP_011524896.1:p.Glu260ArgfsTer?
XM_011526595.1:c.261del	XP_011524897.1:p.Glu88ArgfsTer?
XM_011526595.2:c.261del	XP_011524897.1:p.Glu88ArgfsTer?
XM_017026428.1:c.261del	XP_016881917.1:p.Glu88ArgfsTer?
XM_017026429.1:c.261del	XP_016881918.1:p.Glu88ArgfsTer?
XM_017026430.2:c.261del	XP_016881919.1:p.Glu88ArgfsTer?
NM_139284.3:c.777del MANE Select	NP_644813.1:p.Glu260ArgfsTer?