Canonical Allele Identifier: CA1239262685
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25244160C= , CM000664.2:g.25244160C= GRCh38
NC_000002.11:g.25467029C= , CM000664.1:g.25467029C= GRCh37
NC_000002.10:g.25320533C= NCBI36
NG_029465.2:g.103431G= , LRG_459:g.103431G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.165G=
ENST00000683393.1:c.992G= ENSP00000508654.1:n.992G=
ENST00000683760.1:c.1177G= ENSP00000507765.1:p.Glu393=
ENST00000321117.10:c.1846G= MANE Select ENSP00000324375.5:p.Glu616=
ENST00000264709.7:c.1846G= ENSP00000264709.3:p.Glu616=
ENST00000321117.9:c.1846G= ENSP00000324375.5:p.Glu616=
ENST00000380746.8:c.1279G= ENSP00000370122.4:p.Glu427=
ENST00000380756.7:c.1846G= ENSP00000370132.3:p.Glu616=
ENST00000402667.1:c.1177G= ENSP00000384237.1:p.Glu393=
ENST00000474887.5:n.165G=
NM_022552.4:c.1846G= , LRG_459t1:c.1846G= NP_072046.2:p.Glu616=
NM_153759.3:c.1279G= , LRG_459t2:c.1279G= NP_715640.2:p.Glu427=
NM_175629.2:c.1846G= , LRG_459t4:c.1846G= NP_783328.1:p.Glu616=
XM_005264175.3:c.1846G= XP_005264232.1:p.Glu616=
XM_005264177.3:c.1177G= XP_005264234.1:p.Glu393=
XM_006711957.2:c.1846G= XP_006712020.1:p.Glu616=
XM_006711958.2:c.1402G= XP_006712021.1:p.Glu468=
XM_011532662.1:c.1699G= XP_011530964.1:p.Glu567=
XM_011532663.1:c.1681G= XP_011530965.1:p.Glu561=
XM_011532664.1:c.1846G= XP_011530966.1:p.Glu616=
XM_011532665.1:c.1390G= XP_011530967.1:p.Glu464=
XM_011532666.1:c.1318G= XP_011530968.1:p.Glu440=
XM_011532667.1:c.1177G= XP_011530969.1:p.Glu393=
XM_011532668.1:c.1846G= XP_011530970.1:p.Glu616=
NM_001320893.1:c.1390G= NP_001307822.1:p.Glu464=
NR_135490.1:n.2184G=
XM_005264175.5:c.1846G= XP_005264232.1:p.Glu616=
XM_005264177.4:c.1177G= XP_005264234.1:p.Glu393=
XM_011532662.2:c.1699G= XP_011530964.1:p.Glu567=
XM_011532663.2:c.1681G= XP_011530965.1:p.Glu561=
XM_011532664.2:c.1846G= XP_011530966.1:p.Glu616=
XM_011532666.2:c.1318G= XP_011530968.1:p.Glu440=
XM_011532667.3:c.1177G= XP_011530969.1:p.Glu393=
XM_017003526.1:c.1846G= XP_016859015.1:p.Glu616=
XM_017003527.1:c.1177G= XP_016859016.1:p.Glu393=
XR_001738657.1:n.2123G=
NM_001375819.1:c.1177G= NP_001362748.1:p.Glu393=
NR_135490.2:n.2077G=
NM_022552.5:c.1846G= MANE Select NP_072046.2:p.Glu616=