Canonical Allele Identifier: CA2576072343

Gene: BCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81280801T>G , CM000678.2:g.81280801T>G	GRCh38
NC_000016.9:g.81314406T>G , CM000678.1:g.81314406T>G	GRCh37
NC_000016.8:g.79871907T>G	NCBI36
NG_012171.1:g.47111T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258168.7:c.1102-56T>G MANE Select	ENSP00000258168.2:n.1102-56T>G
ENST00000258168.6:c.1102-56T>G	ENSP00000258168.2:n.1102-56T>G
ENST00000563804.5:c.*726-56T>G	ENSP00000457910.1:n.*726-56T>G
NM_017429.2:c.1102-56T>G	NP_059125.2:n.1102-56T>G
XM_011523109.1:c.1102-6494T>G	XP_011521411.1:n.1102-6494T>G
XM_011523110.1:c.553-56T>G	XP_011521412.1:n.553-56T>G
XM_011523109.2:c.1102-6494T>G	XP_011521411.1:n.1102-6494T>G
XM_017023286.2:c.1102-56T>G	XP_016878775.1:n.1102-56T>G
XM_017023287.2:c.1102-56T>G	XP_016878776.1:n.1102-56T>G
XM_017023288.2:c.1102-56T>G	XP_016878777.1:n.1102-56T>G
XM_017023289.1:c.325-56T>G	XP_016878778.1:n.325-56T>G
XR_002957813.1:n.1429-56T>G
NM_017429.3:c.1102-56T>G MANE Select	NP_059125.2:n.1102-56T>G