Canonical Allele Identifier: CA2333512089

Gene: LGI4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126925_35126926delinsAG , CM000681.2:g.35126925_35126926delinsAG	GRCh38
NC_000019.9:g.35617829_35617830delinsAG , CM000681.1:g.35617829_35617830delinsAG	GRCh37
NC_000019.8:g.40309669_40309670delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.720_721delinsCT MANE Select	ENSP00000312273.3:p.Pro240=
ENST00000310123.7:c.720_721delinsCT	ENSP00000312273.3:p.Pro240=
ENST00000392225.7:c.720_721delinsCT	ENSP00000376059.3:p.Pro240=
ENST00000493050.5:n.779_780delinsCT
ENST00000587780.5:c.455_456delinsCT
ENST00000591840.5:n.420-2060_420-2059delinsCT
ENST00000593248.5:n.851_852delinsCT
NM_139284.2:c.720_721delinsCT	NP_644813.1:p.Pro240=
XM_011526594.1:c.720_721delinsCT	XP_011524896.1:p.Pro240=
XM_011526595.1:c.204_205delinsCT	XP_011524897.1:p.Pro68=
XM_011526595.2:c.204_205delinsCT	XP_011524897.1:p.Pro68=
XM_017026428.1:c.204_205delinsCT	XP_016881917.1:p.Pro68=
XM_017026429.1:c.204_205delinsCT	XP_016881918.1:p.Pro68=
XM_017026430.2:c.204_205delinsCT	XP_016881919.1:p.Pro68=
NM_139284.3:c.720_721delinsCT MANE Select	NP_644813.1:p.Pro240=