Canonical Allele Identifier: CA1239262502
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25243980G= , CM000664.2:g.25243980G= GRCh38
NC_000002.11:g.25466849G= , CM000664.1:g.25466849G= GRCh37
NC_000002.10:g.25320353G= NCBI36
NG_029465.2:g.103611C= , LRG_459:g.103611C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.173C=
ENST00000683393.1:c.1000C= ENSP00000508654.1:n.1000C=
ENST00000683760.1:c.1185C= ENSP00000507765.1:p.Asp395=
ENST00000321117.10:c.1854C= MANE Select ENSP00000324375.5:p.Asp618=
ENST00000264709.7:c.1854C= ENSP00000264709.3:p.Asp618=
ENST00000321117.9:c.1854C= ENSP00000324375.5:p.Asp618=
ENST00000380746.8:c.1287C= ENSP00000370122.4:p.Asp429=
ENST00000380756.7:c.1854C= ENSP00000370132.3:p.Asp618=
ENST00000402667.1:c.1185C= ENSP00000384237.1:p.Asp395=
ENST00000461228.1:n.3C=
ENST00000474887.5:n.173C=
NM_022552.4:c.1854C= , LRG_459t1:c.1854C= NP_072046.2:p.Asp618=
NM_153759.3:c.1287C= , LRG_459t2:c.1287C= NP_715640.2:p.Asp429=
NM_175629.2:c.1854C= , LRG_459t4:c.1854C= NP_783328.1:p.Asp618=
XM_005264175.3:c.1854C= XP_005264232.1:p.Asp618=
XM_005264177.3:c.1185C= XP_005264234.1:p.Asp395=
XM_006711957.2:c.1854C= XP_006712020.1:p.Asp618=
XM_006711958.2:c.1410C= XP_006712021.1:p.Asp470=
XM_011532662.1:c.1707C= XP_011530964.1:p.Asp569=
XM_011532663.1:c.1689C= XP_011530965.1:p.Asp563=
XM_011532664.1:c.1854C= XP_011530966.1:p.Asp618=
XM_011532665.1:c.1398C= XP_011530967.1:p.Asp466=
XM_011532666.1:c.1326C= XP_011530968.1:p.Asp442=
XM_011532667.1:c.1185C= XP_011530969.1:p.Asp395=
XM_011532668.1:c.1854C= XP_011530970.1:p.Asp618=
NM_001320893.1:c.1398C= NP_001307822.1:p.Asp466=
NR_135490.1:n.2192C=
XM_005264175.5:c.1854C= XP_005264232.1:p.Asp618=
XM_005264177.4:c.1185C= XP_005264234.1:p.Asp395=
XM_011532662.2:c.1707C= XP_011530964.1:p.Asp569=
XM_011532663.2:c.1689C= XP_011530965.1:p.Asp563=
XM_011532664.2:c.1854C= XP_011530966.1:p.Asp618=
XM_011532666.2:c.1326C= XP_011530968.1:p.Asp442=
XM_011532667.3:c.1185C= XP_011530969.1:p.Asp395=
XM_017003526.1:c.1854C= XP_016859015.1:p.Asp618=
XM_017003527.1:c.1185C= XP_016859016.1:p.Asp395=
XR_001738657.1:n.2131C=
NM_001375819.1:c.1185C= NP_001362748.1:p.Asp395=
NR_135490.2:n.2085C=
NM_022552.5:c.1854C= MANE Select NP_072046.2:p.Asp618=