Canonical Allele Identifier: CA2576693905
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25240356_25240370del , CM000664.2:g.25240356_25240370del GRCh38
NC_000002.11:g.25463225_25463239del , CM000664.1:g.25463225_25463239del GRCh37
NC_000002.10:g.25316729_25316743del NCBI36
NG_029465.2:g.107221_107235del , LRG_459:g.107221_107235del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.573_587del
ENST00000683393.1:c.1400_1414del ENSP00000508654.1:n.1400_1414del
ENST00000683760.1:c.1585_1599del ENSP00000507765.1:p.Phe529_Glu533del
ENST00000321117.10:c.2254_2268del MANE Select ENSP00000324375.5:p.Phe752_Glu756del
ENST00000264709.7:c.2254_2268del ENSP00000264709.3:p.Phe752_Glu756del
ENST00000321117.9:c.2254_2268del ENSP00000324375.5:p.Phe752_Glu756del
ENST00000380746.8:c.1687_1701del ENSP00000370122.4:p.Phe563_Glu567del
ENST00000380756.7:c.2254_2268del ENSP00000370132.3:p.Phe752_Glu756del
ENST00000402667.1:c.1585_1599del ENSP00000384237.1:p.Phe529_Glu533del
ENST00000461228.1:n.473_487del
ENST00000466601.5:n.626_640del
ENST00000474887.5:n.573_587del
ENST00000482935.5:n.254_268del
ENST00000491288.5:n.310+270_310+284del
NM_022552.4:c.2254_2268del , LRG_459t1:c.2254_2268del NP_072046.2:p.Phe752_Glu756del
NM_153759.3:c.1687_1701del , LRG_459t2:c.1687_1701del NP_715640.2:p.Phe563_Glu567del
NM_175629.2:c.2254_2268del , LRG_459t4:c.2254_2268del NP_783328.1:p.Phe752_Glu756del
XM_005264175.3:c.2254_2268del XP_005264232.1:p.Phe752_Glu756del
XM_005264177.3:c.1585_1599del XP_005264234.1:p.Phe529_Glu533del
XM_006711957.2:c.2254_2268del XP_006712020.1:p.Phe752_Glu756del
XM_006711958.2:c.1810_1824del XP_006712021.1:p.Phe604_Glu608del
XM_011532662.1:c.2107_2121del XP_011530964.1:p.Phe703_Glu707del
XM_011532663.1:c.2089_2103del XP_011530965.1:p.Phe697_Glu701del
XM_011532664.1:c.2254_2268del XP_011530966.1:p.Phe752_Glu756del
XM_011532665.1:c.1798_1812del XP_011530967.1:p.Phe600_Glu604del
XM_011532666.1:c.1726_1740del XP_011530968.1:p.Phe576_Glu580del
XM_011532667.1:c.1585_1599del XP_011530969.1:p.Phe529_Glu533del
XM_011532668.1:c.2254_2268del XP_011530970.1:p.Phe752_Glu756del
NM_001320893.1:c.1798_1812del NP_001307822.1:p.Phe600_Glu604del
NR_135490.1:n.2592_2606del
XM_005264175.5:c.2254_2268del XP_005264232.1:p.Phe752_Glu756del
XM_005264177.4:c.1585_1599del XP_005264234.1:p.Phe529_Glu533del
XM_011532662.2:c.2107_2121del XP_011530964.1:p.Phe703_Glu707del
XM_011532663.2:c.2089_2103del XP_011530965.1:p.Phe697_Glu701del
XM_011532664.2:c.2254_2268del XP_011530966.1:p.Phe752_Glu756del
XM_011532666.2:c.1726_1740del XP_011530968.1:p.Phe576_Glu580del
XM_011532667.3:c.1585_1599del XP_011530969.1:p.Phe529_Glu533del
XM_017003526.1:c.2254_2268del XP_016859015.1:p.Phe752_Glu756del
XM_017003527.1:c.1585_1599del XP_016859016.1:p.Phe529_Glu533del
XR_001738657.1:n.2531_2545del
NM_001375819.1:c.1585_1599del NP_001362748.1:p.Phe529_Glu533del
NR_135490.2:n.2485_2499del
NM_022552.5:c.2254_2268del MANE Select NP_072046.2:p.Phe752_Glu756del