Canonical Allele Identifier: CA351889913

Gene: TOP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25598346A>C , CM000665.2:g.25598346A>C	GRCh38
NC_000003.11:g.25639837A>C , CM000665.1:g.25639837A>C	GRCh37
NC_000003.10:g.25614841A>C	NCBI36
NG_029013.1:g.175084A>C
NG_029013.3:g.774024A>C
NG_052961.1:g.71027T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001330700.2:c.4842T>G MANE Select	NP_001317629.1:p.Asp1614Glu
ENST00000264331.9:c.4842T>G MANE Select	ENSP00000264331.4:p.Asp1614Glu
NM_001068.3:c.4827T>G	NP_001059.2:p.Asp1609Glu
NM_001330700.1:c.4842T>G	NP_001317629.1:p.Asp1614Glu
ENST00000264331.8:c.4842T>G	ENSP00000264331.4:p.Asp1614Glu
ENST00000413971.5:c.1687T>G	ENSP00000388216.1:n.1687T>G
ENST00000435706.6:c.4827T>G	ENSP00000396704.2:p.Asp1609Glu
ENST00000470132.2:n.3741T>G
ENST00000699028.1:n.1705T>G
ENST00000699029.1:n.3772T>G
ENST00000699030.1:n.2948T>G
ENST00000699031.1:n.5105T>G
ENST00000699032.1:n.7480T>G
ENST00000699033.1:n.5213T>G
ENST00000699034.1:n.1599T>G
ENST00000699035.1:n.1318T>G
ENST00000699036.1:n.3470T>G
ENST00000699037.1:c.4515T>G	ENSP00000514096.1:p.Asp1505Glu
ENST00000699038.1:c.*2431T>G	ENSP00000514097.1:n.*2431T>G
ENST00000699039.1:n.1508T>G
ENST00000699040.1:n.2312T>G
ENST00000699041.1:n.3023T>G
ENST00000699042.1:n.2381T>G
XM_005265427.2:c.4842T>G	XP_005265484.1:p.Asp1614Glu
XM_011534057.1:c.4731T>G	XP_011532359.1:p.Asp1577Glu
XM_011534057.3:c.4731T>G	XP_011532359.1:p.Asp1577Glu
XR_001740241.2:n.5344T>G