Canonical Allele Identifier: CA398639821

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208433A>C (hg19) ; chr17:g.18305119A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305119A>C , CM000679.2:g.18305119A>C	GRCh38
NC_000017.10:g.18208433A>C , CM000679.1:g.18208433A>C	GRCh37
NC_000017.9:g.18149158A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.492T>G MANE Select	ENSP00000321636.5:p.Cys164Trp
ENST00000321105.9:c.492T>G	ENSP00000321636.5:p.Cys164Trp
ENST00000461127.5:c.*110T>G	ENSP00000464338.1:n.*110T>G
ENST00000469739.6:n.371T>G
ENST00000542570.5:c.492T>G	ENSP00000442336.2:p.Cys164Trp
ENST00000580095.5:c.417T>G	ENSP00000462790.1:p.Cys139Trp
ENST00000582981.5:c.*148T>G	ENSP00000462378.1:n.*148T>G
ENST00000584582.5:c.*148T>G	ENSP00000462136.1:n.*148T>G
ENST00000584669.5:n.542+1772T>G
NM_004618.3:c.492T>G	NP_004609.1:p.Cys164Trp
XM_005256776.2:c.207T>G	XP_005256833.1:p.Cys69Trp
XM_011524000.1:c.492T>G	XP_011522302.1:p.Cys164Trp
XM_011524001.1:c.-711T>G	XP_011522303.1:n.-711T>G
NM_001320759.1:c.207T>G	NP_001307688.1:p.Cys69Trp
NM_004618.4:c.492T>G	NP_004609.1:p.Cys164Trp
XM_011524001.2:c.-711T>G	XP_011522303.1:n.-711T>G
XM_024450903.1:c.-430T>G	XP_024306671.1:n.-430T>G
XR_001752601.2:n.710T>G
NM_004618.5:c.492T>G MANE Select	NP_004609.1:p.Cys164Trp
NM_001320759.2:c.207T>G	NP_001307688.1:p.Cys69Trp