Canonical Allele Identifier: CA498260342

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208427A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305113A>C , CM000679.2:g.18305113A>C	GRCh38
NC_000017.10:g.18208427A>C , CM000679.1:g.18208427A>C	GRCh37
NC_000017.9:g.18149152A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.498T>G MANE Select	ENSP00000321636.5:p.Ala166=
ENST00000321105.9:c.498T>G	ENSP00000321636.5:p.Ala166=
ENST00000461127.5:c.*116T>G	ENSP00000464338.1:n.*116T>G
ENST00000469739.6:n.377T>G
ENST00000542570.5:c.498T>G	ENSP00000442336.2:p.Ala166=
ENST00000580095.5:c.423T>G	ENSP00000462790.1:p.Ala141=
ENST00000582981.5:c.*154T>G	ENSP00000462378.1:n.*154T>G
ENST00000584582.5:c.*154T>G	ENSP00000462136.1:n.*154T>G
ENST00000584669.5:n.542+1778T>G
NM_004618.3:c.498T>G	NP_004609.1:p.Ala166=
XM_005256776.2:c.213T>G	XP_005256833.1:p.Ala71=
XM_011524000.1:c.498T>G	XP_011522302.1:p.Ala166=
XM_011524001.1:c.-705T>G	XP_011522303.1:n.-705T>G
NM_001320759.1:c.213T>G	NP_001307688.1:p.Ala71=
NM_004618.4:c.498T>G	NP_004609.1:p.Ala166=
XM_011524001.2:c.-705T>G	XP_011522303.1:n.-705T>G
XM_024450903.1:c.-424T>G	XP_024306671.1:n.-424T>G
XR_001752601.2:n.716T>G
NM_004618.5:c.498T>G MANE Select	NP_004609.1:p.Ala166=
NM_001320759.2:c.213T>G	NP_001307688.1:p.Ala71=