Canonical Allele Identifier: CA498260407

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208436C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305122C>T , CM000679.2:g.18305122C>T	GRCh38
NC_000017.10:g.18208436C>T , CM000679.1:g.18208436C>T	GRCh37
NC_000017.9:g.18149161C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321105.10:c.489G>A MANE Select	ENSP00000321636.5:p.Val163=
ENST00000321105.9:c.489G>A	ENSP00000321636.5:p.Val163=
ENST00000461127.5:c.*107G>A	ENSP00000464338.1:n.*107G>A
ENST00000469739.6:n.368G>A
ENST00000542570.5:c.489G>A	ENSP00000442336.2:p.Val163=
ENST00000580095.5:c.414G>A	ENSP00000462790.1:p.Val138=
ENST00000582981.5:c.*145G>A	ENSP00000462378.1:n.*145G>A
ENST00000584582.5:c.*145G>A	ENSP00000462136.1:n.*145G>A
ENST00000584669.5:n.542+1769G>A
NM_004618.3:c.489G>A	NP_004609.1:p.Val163=
XM_005256776.2:c.204G>A	XP_005256833.1:p.Val68=
XM_011524000.1:c.489G>A	XP_011522302.1:p.Val163=
XM_011524001.1:c.-714G>A	XP_011522303.1:n.-714G>A
NM_001320759.1:c.204G>A	NP_001307688.1:p.Val68=
NM_004618.4:c.489G>A	NP_004609.1:p.Val163=
XM_011524001.2:c.-714G>A	XP_011522303.1:n.-714G>A
XM_024450903.1:c.-433G>A	XP_024306671.1:n.-433G>A
XR_001752601.2:n.707G>A
NM_004618.5:c.489G>A MANE Select	NP_004609.1:p.Val163=
NM_001320759.2:c.204G>A	NP_001307688.1:p.Val68=