Canonical Allele Identifier: CA8430292

Gene: TOP3A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18308357C>T , CM000679.2:g.18308357C>T	GRCh38
NC_000017.10:g.18211671C>T , CM000679.1:g.18211671C>T	GRCh37
NC_000017.9:g.18152396C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004618.5:c.308G>A MANE Select	NP_004609.1:p.Arg103Gln
ENST00000321105.10:c.308G>A MANE Select	ENSP00000321636.5:p.Arg103Gln
NM_001320759.1:c.29+525G>A	NP_001307688.1:n.29+525G>A
NM_001320759.2:c.29+525G>A	NP_001307688.1:n.29+525G>A
NM_004618.3:c.308G>A	NP_004609.1:p.Arg103Gln
NM_004618.4:c.308G>A	NP_004609.1:p.Arg103Gln
ENST00000321105.9:c.308G>A	ENSP00000321636.5:p.Arg103Gln
ENST00000461127.5:c.308G>A	ENSP00000464338.1:p.Arg103Gln
ENST00000472959.5:n.490G>A
ENST00000542570.5:c.308G>A	ENSP00000442336.2:p.Arg103Gln
ENST00000580095.5:c.233G>A	ENSP00000462790.1:p.Arg78Gln
ENST00000582230.5:n.499G>A
ENST00000582981.5:c.240+525G>A	ENSP00000462378.1:n.240+525G>A
ENST00000583328.5:n.304G>A
ENST00000584582.5:c.181-1391G>A	ENSP00000462136.1:n.181-1391G>A
ENST00000584669.5:n.460G>A
ENST00000584887.1:n.500G>A
ENST00000585031.2:c.252+56G>A	ENSP00000464493.1:n.252+56G>A
XM_005256776.2:c.29+525G>A	XP_005256833.1:n.29+525G>A
XM_011524000.1:c.308G>A	XP_011522302.1:p.Arg103Gln
XM_024450903.1:c.-652G>A	XP_024306671.1:n.-652G>A
XR_001752601.2:n.526G>A