Canonical Allele Identifier: CA2497030038

Gene: TOP2B

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25629059_25629061del , CM000665.2:g.25629059_25629061del	GRCh38
NC_000003.11:g.25670550_25670552del , CM000665.1:g.25670550_25670552del	GRCh37
NC_000003.10:g.25645554_25645556del	NCBI36
NG_052961.1:g.40314_40316del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699031.1:n.1620_1622del
ENST00000699032.1:n.1620_1622del
ENST00000699033.1:n.1620_1622del
ENST00000699037.1:c.1533_1535del	ENSP00000514096.1:p.Glu512del
ENST00000699038.1:c.1533_1535del	ENSP00000514097.1:p.Glu512del
ENST00000699043.1:c.1533_1535del	ENSP00000514098.1:p.Glu512del
ENST00000699044.1:n.1620_1622del
ENST00000699046.1:n.903_905del
ENST00000264331.9:c.1776_1778del MANE Select	ENSP00000264331.4:p.Glu593del
ENST00000264331.8:c.1776_1778del	ENSP00000264331.4:p.Glu593del
ENST00000424225.1:c.1761_1763del	ENSP00000391112.1:p.Glu588del
ENST00000435706.6:c.1761_1763del	ENSP00000396704.2:p.Glu588del
ENST00000491510.1:n.214_216del
NM_001068.3:c.1761_1763del	NP_001059.2:p.Glu588del
XM_005265427.2:c.1776_1778del	XP_005265484.1:p.Glu593del
XM_011534057.1:c.1776_1778del	XP_011532359.1:p.Glu593del
XR_940497.1:n.2384_2386del
NM_001330700.1:c.1776_1778del	NP_001317629.1:p.Glu593del
XM_011534057.3:c.1776_1778del	XP_011532359.1:p.Glu593del
XR_001740241.2:n.2370_2372del
NM_001330700.2:c.1776_1778del MANE Select	NP_001317629.1:p.Glu593del