Canonical Allele Identifier: CA398639769

Gene: TOP3A

Linked Data

• MyVariant Identifiers: chr17:g.18208429C>T (hg19) ; chr17:g.18305115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18305115C>T , CM000679.2:g.18305115C>T	GRCh38
NC_000017.10:g.18208429C>T , CM000679.1:g.18208429C>T	GRCh37
NC_000017.9:g.18149154C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321105.10:c.496G>A MANE Select	ENSP00000321636.5:p.Ala166Thr
ENST00000321105.9:c.496G>A	ENSP00000321636.5:p.Ala166Thr
ENST00000461127.5:c.*114G>A	ENSP00000464338.1:n.*114G>A
ENST00000469739.6:n.375G>A
ENST00000542570.5:c.496G>A	ENSP00000442336.2:p.Ala166Thr
ENST00000580095.5:c.421G>A	ENSP00000462790.1:p.Ala141Thr
ENST00000582981.5:c.*152G>A	ENSP00000462378.1:n.*152G>A
ENST00000584582.5:c.*152G>A	ENSP00000462136.1:n.*152G>A
ENST00000584669.5:n.542+1776G>A
NM_004618.3:c.496G>A	NP_004609.1:p.Ala166Thr
XM_005256776.2:c.211G>A	XP_005256833.1:p.Ala71Thr
XM_011524000.1:c.496G>A	XP_011522302.1:p.Ala166Thr
XM_011524001.1:c.-707G>A	XP_011522303.1:n.-707G>A
NM_001320759.1:c.211G>A	NP_001307688.1:p.Ala71Thr
NM_004618.4:c.496G>A	NP_004609.1:p.Ala166Thr
XM_011524001.2:c.-707G>A	XP_011522303.1:n.-707G>A
XM_024450903.1:c.-426G>A	XP_024306671.1:n.-426G>A
XR_001752601.2:n.714G>A
NM_004618.5:c.496G>A MANE Select	NP_004609.1:p.Ala166Thr
NM_001320759.2:c.211G>A	NP_001307688.1:p.Ala71Thr