Canonical Allele Identifier: CA1239265165
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25240340C= , CM000664.2:g.25240340C= GRCh38
NC_000002.11:g.25463209C= , CM000664.1:g.25463209C= GRCh37
NC_000002.10:g.25316713C= NCBI36
NG_029465.2:g.107251G= , LRG_459:g.107251G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.603G=
ENST00000683393.1:c.1430G= ENSP00000508654.1:n.1430G=
ENST00000683760.1:c.1615G= ENSP00000507765.1:p.Gly539=
ENST00000321117.10:c.2284G= MANE Select ENSP00000324375.5:p.Gly762=
ENST00000264709.7:c.2284G= ENSP00000264709.3:p.Gly762=
ENST00000321117.9:c.2284G= ENSP00000324375.5:p.Gly762=
ENST00000380746.8:c.1717G= ENSP00000370122.4:p.Gly573=
ENST00000380756.7:c.2284G= ENSP00000370132.3:p.Gly762=
ENST00000402667.1:c.1615G= ENSP00000384237.1:p.Gly539=
ENST00000461228.1:n.503G=
ENST00000466601.5:n.656G=
ENST00000474887.5:n.603G=
ENST00000482935.5:n.284G=
ENST00000491288.5:n.310+300G=
NM_022552.4:c.2284G= , LRG_459t1:c.2284G= NP_072046.2:p.Gly762=
NM_153759.3:c.1717G= , LRG_459t2:c.1717G= NP_715640.2:p.Gly573=
NM_175629.2:c.2284G= , LRG_459t4:c.2284G= NP_783328.1:p.Gly762=
XM_005264175.3:c.2284G= XP_005264232.1:p.Gly762=
XM_005264177.3:c.1615G= XP_005264234.1:p.Gly539=
XM_006711957.2:c.2284G= XP_006712020.1:p.Gly762=
XM_006711958.2:c.1840G= XP_006712021.1:p.Gly614=
XM_011532662.1:c.2137G= XP_011530964.1:p.Gly713=
XM_011532663.1:c.2119G= XP_011530965.1:p.Gly707=
XM_011532664.1:c.2284G= XP_011530966.1:p.Gly762=
XM_011532665.1:c.1828G= XP_011530967.1:p.Gly610=
XM_011532666.1:c.1756G= XP_011530968.1:p.Gly586=
XM_011532667.1:c.1615G= XP_011530969.1:p.Gly539=
XM_011532668.1:c.2284G= XP_011530970.1:p.Gly762=
NM_001320893.1:c.1828G= NP_001307822.1:p.Gly610=
NR_135490.1:n.2622G=
XM_005264175.5:c.2284G= XP_005264232.1:p.Gly762=
XM_005264177.4:c.1615G= XP_005264234.1:p.Gly539=
XM_011532662.2:c.2137G= XP_011530964.1:p.Gly713=
XM_011532663.2:c.2119G= XP_011530965.1:p.Gly707=
XM_011532664.2:c.2284G= XP_011530966.1:p.Gly762=
XM_011532666.2:c.1756G= XP_011530968.1:p.Gly586=
XM_011532667.3:c.1615G= XP_011530969.1:p.Gly539=
XM_017003526.1:c.2284G= XP_016859015.1:p.Gly762=
XM_017003527.1:c.1615G= XP_016859016.1:p.Gly539=
XR_001738657.1:n.2561G=
NM_001375819.1:c.1615G= NP_001362748.1:p.Gly539=
NR_135490.2:n.2515G=
NM_022552.5:c.2284G= MANE Select NP_072046.2:p.Gly762=