Canonical Allele Identifier: CA405313262

Gene: LGI4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35131510C>A , CM000681.2:g.35131510C>A	GRCh38
NC_000019.9:g.35622414C>A , CM000681.1:g.35622414C>A	GRCh37
NC_000019.8:g.40314254C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_139284.3:c.504G>T MANE Select	NP_644813.1:p.Trp168Cys
ENST00000310123.8:c.504G>T MANE Select	ENSP00000312273.3:p.Trp168Cys
NM_139284.2:c.504G>T	NP_644813.1:p.Trp168Cys
ENST00000310123.7:c.504G>T	ENSP00000312273.3:p.Trp168Cys
ENST00000392225.7:c.504G>T	ENSP00000376059.3:p.Trp168Cys
ENST00000473160.6:n.730G>T
ENST00000493050.5:n.563G>T
ENST00000587780.5:c.239G>T
ENST00000591633.2:c.504G>T	ENSP00000467784.1:p.Trp168Cys
ENST00000591840.5:n.419+281G>T
ENST00000593248.5:n.635G>T
XM_011526594.1:c.504G>T	XP_011524896.1:p.Trp168Cys
XM_011526595.1:c.-13G>T	XP_011524897.1:n.-13G>T
XM_011526595.2:c.-13G>T	XP_011524897.1:n.-13G>T
XM_017026428.1:c.-13G>T	XP_016881917.1:n.-13G>T
XM_017026429.1:c.-13G>T	XP_016881918.1:n.-13G>T
XM_017026430.2:c.-13G>T	XP_016881919.1:n.-13G>T