Canonical Allele Identifier: CA398639804
Gene: TOP3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18305117T>A , CM000679.2:g.18305117T>A GRCh38
NC_000017.10:g.18208431T>A , CM000679.1:g.18208431T>A GRCh37
NC_000017.9:g.18149156T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321105.10:c.494A>T MANE Select ENSP00000321636.5:p.Lys165Met
ENST00000321105.9:c.494A>T ENSP00000321636.5:p.Lys165Met
ENST00000461127.5:c.*112A>T ENSP00000464338.1:n.*112A>T
ENST00000469739.6:n.373A>T
ENST00000542570.5:c.494A>T ENSP00000442336.2:p.Lys165Met
ENST00000580095.5:c.419A>T ENSP00000462790.1:p.Lys140Met
ENST00000582981.5:c.*150A>T ENSP00000462378.1:n.*150A>T
ENST00000584582.5:c.*150A>T ENSP00000462136.1:n.*150A>T
ENST00000584669.5:n.542+1774A>T
NM_004618.3:c.494A>T NP_004609.1:p.Lys165Met
XM_005256776.2:c.209A>T XP_005256833.1:p.Lys70Met
XM_011524000.1:c.494A>T XP_011522302.1:p.Lys165Met
XM_011524001.1:c.-709A>T XP_011522303.1:n.-709A>T
NM_001320759.1:c.209A>T NP_001307688.1:p.Lys70Met
NM_004618.4:c.494A>T NP_004609.1:p.Lys165Met
XM_011524001.2:c.-709A>T XP_011522303.1:n.-709A>T
XM_024450903.1:c.-428A>T XP_024306671.1:n.-428A>T
XR_001752601.2:n.712A>T
NM_004618.5:c.494A>T MANE Select NP_004609.1:p.Lys165Met
NM_001320759.2:c.209A>T NP_001307688.1:p.Lys70Met