Canonical Allele Identifier: CA2577367519
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787279del , CM000682.2:g.32787279del GRCh38
NC_000020.10:g.31375085del , CM000682.1:g.31375085del GRCh37
NC_000020.9:g.30838746del NCBI36
NG_007290.1:g.29895del , LRG_56:g.29895del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.482del ENSP00000512497.1:p.Pro161LeufsTer?
ENST00000696232.1:c.482del ENSP00000512498.1:p.Pro161LeufsTer?
ENST00000696233.1:c.482del ENSP00000512499.1:p.Pro161LeufsTer?
ENST00000696234.1:n.466del
ENST00000696235.1:c.356del ENSP00000512500.1:p.Pro119LeufsTer?
ENST00000696236.1:c.356del ENSP00000512501.1:p.Pro119LeufsTer?
ENST00000696237.1:n.588del
ENST00000696238.1:c.482del ENSP00000512502.1:p.Pro161LeufsTer?
ENST00000696239.1:c.482del ENSP00000512503.1:p.Pro161LeufsTer?
ENST00000201963.3:c.518del ENSP00000201963.3:p.Pro173LeufsTer?
ENST00000328111.6:c.482del MANE Select ENSP00000328547.2:p.Pro161LeufsTer?
ENST00000348286.6:c.482del ENSP00000337764.2:p.Pro161LeufsTer?
ENST00000353855.6:c.482del ENSP00000313397.4:p.Pro161LeufsTer?
ENST00000443239.7:c.356del ENSP00000403169.2:p.Pro119LeufsTer?
ENST00000456297.6:c.254del ENSP00000412305.1:p.Pro85LeufsTer?
NM_001207055.1:c.356del NP_001193984.1:p.Pro119LeufsTer?
NM_001207056.1:c.254del NP_001193985.1:p.Pro85LeufsTer?
NM_006892.3:c.482del , LRG_56t1:c.482del NP_008823.1:p.Pro161LeufsTer?
NM_175848.1:c.482del NP_787044.1:p.Pro161LeufsTer?
NM_175849.1:c.482del NP_787045.1:p.Pro161LeufsTer?
NM_175850.2:c.518del NP_787046.1:p.Pro173LeufsTer?
XM_011528653.1:c.518del XP_011526955.1:p.Pro173LeufsTer?
XM_011528654.1:c.392del XP_011526956.1:p.Pro131LeufsTer?
XR_936510.1:n.654del
XR_936511.1:n.654del
XR_936512.1:n.529del
XM_011528653.2:c.518del XP_011526955.1:p.Pro173LeufsTer?
XM_011528654.2:c.392del XP_011526956.1:p.Pro131LeufsTer?
XR_936510.2:n.665del
XR_936511.2:n.665del
XR_936512.2:n.541del
NM_001207055.2:c.356del NP_001193984.1:p.Pro119LeufsTer?
NM_001207056.2:c.254del NP_001193985.1:p.Pro85LeufsTer?
NM_006892.4:c.482del MANE Select NP_008823.1:p.Pro161LeufsTer?
NM_175848.2:c.482del NP_787044.1:p.Pro161LeufsTer?
NM_175849.2:c.482del NP_787045.1:p.Pro161LeufsTer?
NM_175850.3:c.518del NP_787046.1:p.Pro173LeufsTer?