Canonical Allele Identifier: CA2333512052

Gene: LGI4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35126858A= , CM000681.2:g.35126858A=	GRCh38
NC_000019.9:g.35617762A= , CM000681.1:g.35617762A=	GRCh37
NC_000019.8:g.40309602A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310123.8:c.788T= MANE Select	ENSP00000312273.3:p.Leu263=
ENST00000310123.7:c.788T=	ENSP00000312273.3:p.Leu263=
ENST00000392225.7:c.788T=	ENSP00000376059.3:p.Leu263=
ENST00000493050.5:n.847T=
ENST00000587780.5:c.523T=
ENST00000591840.5:n.420-1992T=
ENST00000593248.5:n.919T=
NM_139284.2:c.788T=	NP_644813.1:p.Leu263=
XM_011526594.1:c.788T=	XP_011524896.1:p.Leu263=
XM_011526595.1:c.272T=	XP_011524897.1:p.Leu91=
XM_011526595.2:c.272T=	XP_011524897.1:p.Leu91=
XM_017026428.1:c.272T=	XP_016881917.1:p.Leu91=
XM_017026429.1:c.272T=	XP_016881918.1:p.Leu91=
XM_017026430.2:c.272T=	XP_016881919.1:p.Leu91=
NM_139284.3:c.788T= MANE Select	NP_644813.1:p.Leu263=