Canonical Allele Identifier: CA398639711

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208424A>G (hg19) ; chr17:g.18305110A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305110A>G , CM000679.2:g.18305110A>G	GRCh38
NC_000017.10:g.18208424A>G , CM000679.1:g.18208424A>G	GRCh37
NC_000017.9:g.18149149A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321105.10:c.499+2T>C MANE Select	ENSP00000321636.5:n.499+2T>C
ENST00000321105.9:c.499+2T>C	ENSP00000321636.5:n.499+2T>C
ENST00000461127.5:c.*117+2T>C	ENSP00000464338.1:n.*117+2T>C
ENST00000469739.6:n.378+2T>C
ENST00000542570.5:c.499+2T>C	ENSP00000442336.2:n.499+2T>C
ENST00000580095.5:c.424+2T>C	ENSP00000462790.1:n.424+2T>C
ENST00000582981.5:c.*155+2T>C	ENSP00000462378.1:n.*155+2T>C
ENST00000584582.5:c.*155+2T>C	ENSP00000462136.1:n.*155+2T>C
ENST00000584669.5:n.542+1781T>C
NM_004618.3:c.499+2T>C	NP_004609.1:n.499+2T>C
XM_005256776.2:c.214+2T>C	XP_005256833.1:n.214+2T>C
XM_011524000.1:c.499+2T>C	XP_011522302.1:n.499+2T>C
XM_011524001.1:c.-704+2T>C	XP_011522303.1:n.-704+2T>C
NM_001320759.1:c.214+2T>C	NP_001307688.1:n.214+2T>C
NM_004618.4:c.499+2T>C	NP_004609.1:n.499+2T>C
XM_011524001.2:c.-704+2T>C	XP_011522303.1:n.-704+2T>C
XM_024450903.1:c.-423+2T>C	XP_024306671.1:n.-423+2T>C
XR_001752601.2:n.717+2T>C
NM_004618.5:c.499+2T>C MANE Select	NP_004609.1:n.499+2T>C
NM_001320759.2:c.214+2T>C	NP_001307688.1:n.214+2T>C