Canonical Allele Identifier: CA2236989525

Gene: BCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81267946G= , CM000678.2:g.81267946G=	GRCh38
NC_000016.9:g.81301551G= , CM000678.1:g.81301551G=	GRCh37
NC_000016.8:g.79859052G=	NCBI36
NG_012171.1:g.34256G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258168.7:c.658G= MANE Select	ENSP00000258168.2:p.Glu220=
ENST00000258168.6:c.658G=	ENSP00000258168.2:p.Glu220=
ENST00000563804.5:c.*282G=	ENSP00000457910.1:n.*282G=
NM_017429.2:c.658G=	NP_059125.2:p.Glu220=
XM_011523109.1:c.658G=	XP_011521411.1:p.Glu220=
XM_011523110.1:c.109G=	XP_011521412.1:p.Glu37=
XM_011523109.2:c.658G=	XP_011521411.1:p.Glu220=
XM_017023286.2:c.658G=	XP_016878775.1:p.Glu220=
XM_017023287.2:c.658G=	XP_016878776.1:p.Glu220=
XM_017023288.2:c.658G=	XP_016878777.1:p.Glu220=
XM_017023289.1:c.-24-96G=	XP_016878778.1:n.-24-96G=
XR_002957813.1:n.1081-96G=
NM_017429.3:c.658G= MANE Select	NP_059125.2:p.Glu220=