Canonical Allele Identifier: CA510469087
Gene: DNMT3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.31375160del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32787358del , CM000682.2:g.32787358del GRCh38
NC_000020.10:g.31375164del , CM000682.1:g.31375164del GRCh37
NC_000020.9:g.30838825del NCBI36
NG_007290.1:g.29974del , LRG_56:g.29974del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.561del ENSP00000512497.1:p.Tyr188ThrfsTer4
ENST00000696232.1:c.561del ENSP00000512498.1:p.Tyr188ThrfsTer4
ENST00000696233.1:c.561del ENSP00000512499.1:p.Tyr188ThrfsTer4
ENST00000696234.1:n.545del
ENST00000696235.1:c.435del ENSP00000512500.1:p.Tyr146ThrfsTer4
ENST00000696236.1:c.435del ENSP00000512501.1:p.Tyr146ThrfsTer4
ENST00000696237.1:n.667del
ENST00000696238.1:c.561del ENSP00000512502.1:p.Tyr188ThrfsTer4
ENST00000696239.1:c.561del ENSP00000512503.1:p.Tyr188ThrfsTer4
ENST00000201963.3:c.597del ENSP00000201963.3:p.Tyr200ThrfsTer4
ENST00000328111.6:c.561del MANE Select ENSP00000328547.2:p.Tyr188ThrfsTer4
ENST00000348286.6:c.561del ENSP00000337764.2:p.Tyr188ThrfsTer4
ENST00000353855.6:c.561del ENSP00000313397.4:p.Tyr188ThrfsTer4
ENST00000443239.7:c.435del ENSP00000403169.2:p.Tyr146ThrfsTer4
ENST00000456297.6:c.333del ENSP00000412305.1:p.Tyr112ThrfsTer4
NM_001207055.1:c.435del NP_001193984.1:p.Tyr146ThrfsTer4
NM_001207056.1:c.333del NP_001193985.1:p.Tyr112ThrfsTer4
NM_006892.3:c.561del , LRG_56t1:c.561del NP_008823.1:p.Tyr188ThrfsTer4
NM_175848.1:c.561del NP_787044.1:p.Tyr188ThrfsTer4
NM_175849.1:c.561del NP_787045.1:p.Tyr188ThrfsTer4
NM_175850.2:c.597del NP_787046.1:p.Tyr200ThrfsTer4
XM_011528653.1:c.597del XP_011526955.1:p.Tyr200ThrfsTer4
XM_011528654.1:c.471del XP_011526956.1:p.Tyr158ThrfsTer4
XR_936510.1:n.733del
XR_936511.1:n.733del
XR_936512.1:n.608del
XM_011528653.2:c.597del XP_011526955.1:p.Tyr200ThrfsTer4
XM_011528654.2:c.471del XP_011526956.1:p.Tyr158ThrfsTer4
XR_936510.2:n.744del
XR_936511.2:n.744del
XR_936512.2:n.620del
NM_001207055.2:c.435del NP_001193984.1:p.Tyr146ThrfsTer4
NM_001207056.2:c.333del NP_001193985.1:p.Tyr112ThrfsTer4
NM_006892.4:c.561del MANE Select NP_008823.1:p.Tyr188ThrfsTer4
NM_175848.2:c.561del NP_787044.1:p.Tyr188ThrfsTer4
NM_175849.2:c.561del NP_787045.1:p.Tyr188ThrfsTer4
NM_175850.3:c.597del NP_787046.1:p.Tyr200ThrfsTer4