Canonical Allele Identifier: CA1028525432
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234418del , CM000664.2:g.25234418del GRCh38
NC_000002.11:g.25457287del , CM000664.1:g.25457287del GRCh37
NC_000002.10:g.25310791del NCBI36
NG_029465.2:g.113173del , LRG_459:g.113173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.849del
ENST00000683393.1:c.1746del ENSP00000508654.1:n.1746del
ENST00000683760.1:c.1931del ENSP00000507765.1:p.Val644AspfsTer14
ENST00000321117.10:c.2600del MANE Select ENSP00000324375.5:p.Val867AspfsTer14
ENST00000264709.7:c.2600del ENSP00000264709.3:p.Val867AspfsTer14
ENST00000321117.9:c.2600del ENSP00000324375.5:p.Val867AspfsTer14
ENST00000380746.8:c.2033del ENSP00000370122.4:p.Val678AspfsTer14
ENST00000380756.7:c.*453del ENSP00000370132.3:n.*453del
ENST00000402667.1:c.1931del ENSP00000384237.1:p.Val644AspfsTer14
NM_022552.4:c.2600del , LRG_459t1:c.2600del NP_072046.2:p.Val867AspfsTer14
NM_153759.3:c.2033del , LRG_459t2:c.2033del NP_715640.2:p.Val678AspfsTer14
NM_175629.2:c.2600del , LRG_459t4:c.2600del NP_783328.1:p.Val867AspfsTer14
XM_005264175.3:c.2600del XP_005264232.1:p.Val867AspfsTer14
XM_005264177.3:c.1931del XP_005264234.1:p.Val644AspfsTer14
XM_006711958.2:c.2156del XP_006712021.1:p.Val719AspfsTer14
XM_011532662.1:c.2453del XP_011530964.1:p.Val818AspfsTer14
XM_011532663.1:c.2435del XP_011530965.1:p.Val812AspfsTer14
XM_011532665.1:c.2144del XP_011530967.1:p.Val715AspfsTer14
XM_011532666.1:c.2072del XP_011530968.1:p.Val691AspfsTer14
XM_011532667.1:c.1931del XP_011530969.1:p.Val644AspfsTer14
NM_001320893.1:c.2144del NP_001307822.1:p.Val715AspfsTer14
NR_135490.1:n.3137del
XM_005264175.5:c.2600del XP_005264232.1:p.Val867AspfsTer14
XM_005264177.4:c.1931del XP_005264234.1:p.Val644AspfsTer14
XM_011532662.2:c.2453del XP_011530964.1:p.Val818AspfsTer14
XM_011532663.2:c.2435del XP_011530965.1:p.Val812AspfsTer14
XM_011532666.2:c.2072del XP_011530968.1:p.Val691AspfsTer14
XM_011532667.3:c.1931del XP_011530969.1:p.Val644AspfsTer14
XM_017003526.1:c.2600del XP_016859015.1:p.Val867AspfsTer14
XM_017003527.1:c.1931del XP_016859016.1:p.Val644AspfsTer14
XR_001738657.1:n.2807del
NM_001375819.1:c.1931del NP_001362748.1:p.Val644AspfsTer14
NR_135490.2:n.3030del
NM_022552.5:c.2600del MANE Select NP_072046.2:p.Val867AspfsTer14