Canonical Allele Identifier: CA2236942885

Gene: BCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81280704T= , CM000678.2:g.81280704T=	GRCh38
NC_000016.9:g.81314309T= , CM000678.1:g.81314309T=	GRCh37
NC_000016.8:g.79871810T=	NCBI36
NG_012171.1:g.47014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258168.7:c.1102-153T= MANE Select	ENSP00000258168.2:n.1102-153T=
ENST00000258168.6:c.1102-153T=	ENSP00000258168.2:n.1102-153T=
ENST00000563804.5:c.*726-153T=	ENSP00000457910.1:n.*726-153T=
NM_017429.2:c.1102-153T=	NP_059125.2:n.1102-153T=
XM_011523109.1:c.1102-6591T=	XP_011521411.1:n.1102-6591T=
XM_011523110.1:c.553-153T=	XP_011521412.1:n.553-153T=
XM_011523109.2:c.1102-6591T=	XP_011521411.1:n.1102-6591T=
XM_017023286.2:c.1102-153T=	XP_016878775.1:n.1102-153T=
XM_017023287.2:c.1102-153T=	XP_016878776.1:n.1102-153T=
XM_017023288.2:c.1102-153T=	XP_016878777.1:n.1102-153T=
XM_017023289.1:c.325-153T=	XP_016878778.1:n.325-153T=
XR_002957813.1:n.1429-153T=
NM_017429.3:c.1102-153T= MANE Select	NP_059125.2:n.1102-153T=