Canonical Allele Identifier: CA2333512002

Gene: LGI4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126753C= , CM000681.2:g.35126753C=	GRCh38
NC_000019.9:g.35617657C= , CM000681.1:g.35617657C=	GRCh37
NC_000019.8:g.40309497C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.816G= MANE Select	ENSP00000312273.3:p.Lys272=
ENST00000310123.7:c.816G=	ENSP00000312273.3:p.Lys272=
ENST00000392225.7:c.893G=	ENSP00000376059.3:p.Ser298=
ENST00000493050.5:n.875G=
ENST00000587780.5:c.551G=
ENST00000591840.5:n.420-1887G=
ENST00000593248.5:n.1024G=
NM_139284.2:c.816G=	NP_644813.1:p.Lys272=
XM_011526594.1:c.816G=	XP_011524896.1:p.Lys272=
XM_011526595.1:c.300G=	XP_011524897.1:p.Lys100=
XM_011526595.2:c.300G=	XP_011524897.1:p.Lys100=
XM_017026428.1:c.300G=	XP_016881917.1:p.Lys100=
XM_017026429.1:c.300G=	XP_016881918.1:p.Lys100=
XM_017026430.2:c.300G=	XP_016881919.1:p.Lys100=
NM_139284.3:c.816G= MANE Select	NP_644813.1:p.Lys272=