Canonical Allele Identifier: CA10125298

Gene: TOP3B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21957510G>A , CM000684.2:g.21957510G>A	GRCh38
NC_000022.10:g.22311882G>A , CM000684.1:g.22311882G>A	GRCh37
NC_000022.9:g.20641882G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001282112.2:c.2193C>T MANE Select	NP_001269041.1:p.Ser731=
ENST00000357179.10:c.2193C>T MANE Select	ENSP00000349705.5:p.Ser731=
NM_001282112.1:c.2193C>T	NP_001269041.1:p.Ser731=
NM_001282113.1:c.2193C>T	NP_001269042.1:p.Ser731=
NM_001282113.2:c.2193C>T	NP_001269042.1:p.Ser731=
NM_001349845.1:c.2193C>T	NP_001336774.1:p.Ser731=
NM_001349845.2:c.2193C>T	NP_001336774.1:p.Ser731=
NM_001349847.1:c.2193C>T	NP_001336776.1:p.Ser731=
NM_001349847.2:c.2193C>T	NP_001336776.1:p.Ser731=
NM_001349848.1:c.1785C>T	NP_001336777.1:p.Ser595=
NM_001349848.2:c.1785C>T	NP_001336777.1:p.Ser595=
NM_001349850.1:c.1785C>T	NP_001336779.1:p.Ser595=
NM_001349850.2:c.1785C>T	NP_001336779.1:p.Ser595=
NM_001349851.1:c.*896C>T	NP_001336780.1:n.*896C>T
NM_001349851.2:c.*896C>T	NP_001336780.1:n.*896C>T
NM_001349852.1:c.*896C>T	NP_001336781.1:n.*896C>T
NM_001349852.2:c.*896C>T	NP_001336781.1:n.*896C>T
NM_003935.4:c.2193C>T	NP_003926.1:p.Ser731=
NM_003935.5:c.2193C>T	NP_003926.1:p.Ser731=
NR_146277.1:n.3319C>T
NR_146277.2:n.3263C>T
ENST00000357179.9:c.2193C>T	ENSP00000349705.5:p.Ser731=
ENST00000398793.6:c.2193C>T	ENSP00000381773.2:p.Ser731=
ENST00000436282.1:c.2412C>T	ENSP00000416451.1:n.2412C>T
ENST00000444502.5:c.*3135C>T	ENSP00000392480.1:n.*3135C>T
ENST00000457179.5:c.*2029C>T	ENSP00000397221.1:n.*2029C>T
ENST00000457270.5:c.2473C>T
XM_005261811.1:c.2193C>T	XP_005261868.1:p.Ser731=
XM_005261813.1:c.1785C>T	XP_005261870.1:p.Ser595=
XM_006724349.1:c.2193C>T	XP_006724412.1:p.Ser731=
XM_006724350.1:c.2193C>T	XP_006724413.1:p.Ser731=
XM_011530482.1:c.2193C>T	XP_011528784.1:p.Ser731=
XM_011530483.1:c.2193C>T	XP_011528785.1:p.Ser731=
XM_017029038.2:c.2107+982C>T	XP_016884527.1:n.2107+982C>T
XM_024452297.1:c.2193C>T	XP_024308065.1:p.Ser731=
XR_001755353.2:n.2289+982C>T
XR_001755355.2:n.2676C>T
XR_001755357.2:n.2364C>T
XR_001755359.1:n.3341C>T
XR_937945.1:n.3216C>T