Canonical Allele Identifier: CA163301
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25247715_25247717del , CM000664.2:g.25247715_25247717del GRCh38
NC_000002.11:g.25470584_25470586del , CM000664.1:g.25470584_25470586del GRCh37
NC_000002.10:g.25324088_25324090del NCBI36
NG_029465.2:g.99875_99877del , LRG_459:g.99875_99877del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683760.1:c.220_222del ENSP00000507765.1:p.Trp74del
ENST00000321117.10:c.889_891del MANE Select ENSP00000324375.5:p.Trp297del
ENST00000264709.7:c.889_891del ENSP00000264709.3:p.Trp297del
ENST00000321117.9:c.889_891del ENSP00000324375.5:p.Trp297del
ENST00000380746.8:c.322_324del ENSP00000370122.4:p.Trp108del
ENST00000380756.7:c.889_891del ENSP00000370132.3:p.Trp297del
ENST00000402667.1:c.220_222del ENSP00000384237.1:p.Trp74del
ENST00000470983.5:n.336_338del
ENST00000474807.5:n.184_186del
ENST00000496570.1:n.422_424del
NM_022552.4:c.889_891del , LRG_459t1:c.889_891del NP_072046.2:p.Trp297del
NM_153759.3:c.322_324del , LRG_459t2:c.322_324del NP_715640.2:p.Trp108del
NM_175629.2:c.889_891del , LRG_459t4:c.889_891del NP_783328.1:p.Trp297del
XM_005264175.3:c.889_891del XP_005264232.1:p.Trp297del
XM_005264177.3:c.220_222del XP_005264234.1:p.Trp74del
XM_006711957.2:c.889_891del XP_006712020.1:p.Trp297del
XM_006711958.2:c.445_447del XP_006712021.1:p.Trp149del
XM_011532662.1:c.742_744del XP_011530964.1:p.Trp248del
XM_011532663.1:c.724_726del XP_011530965.1:p.Trp242del
XM_011532664.1:c.889_891del XP_011530966.1:p.Trp297del
XM_011532665.1:c.433_435del XP_011530967.1:p.Trp145del
XM_011532666.1:c.361_363del XP_011530968.1:p.Trp121del
XM_011532667.1:c.220_222del XP_011530969.1:p.Trp74del
XM_011532668.1:c.889_891del XP_011530970.1:p.Trp297del
NM_001320893.1:c.433_435del NP_001307822.1:p.Trp145del
NR_135490.1:n.1227_1229del
XM_005264175.5:c.889_891del XP_005264232.1:p.Trp297del
XM_005264177.4:c.220_222del XP_005264234.1:p.Trp74del
XM_011532662.2:c.742_744del XP_011530964.1:p.Trp248del
XM_011532663.2:c.724_726del XP_011530965.1:p.Trp242del
XM_011532664.2:c.889_891del XP_011530966.1:p.Trp297del
XM_011532666.2:c.361_363del XP_011530968.1:p.Trp121del
XM_011532667.3:c.220_222del XP_011530969.1:p.Trp74del
XM_017003526.1:c.889_891del XP_016859015.1:p.Trp297del
XM_017003527.1:c.220_222del XP_016859016.1:p.Trp74del
XR_001738657.1:n.1166_1168del
NM_001375819.1:c.220_222del NP_001362748.1:p.Trp74del
NR_135490.2:n.1120_1122del
NM_022552.5:c.889_891del MANE Select NP_072046.2:p.Trp297del