Canonical Allele Identifier: CA1028509563
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25243980del , CM000664.2:g.25243980del GRCh38
NC_000002.11:g.25466849del , CM000664.1:g.25466849del GRCh37
NC_000002.10:g.25320353del NCBI36
NG_029465.2:g.103613del , LRG_459:g.103613del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.175del
ENST00000683393.1:c.1002del ENSP00000508654.1:n.1002del
ENST00000683760.1:c.1187del ENSP00000507765.1:p.Pro396LeufsTer?
ENST00000321117.10:c.1856del MANE Select ENSP00000324375.5:p.Pro619LeufsTer?
ENST00000264709.7:c.1856del ENSP00000264709.3:p.Pro619LeufsTer?
ENST00000321117.9:c.1856del ENSP00000324375.5:p.Pro619LeufsTer?
ENST00000380746.8:c.1289del ENSP00000370122.4:p.Pro430LeufsTer?
ENST00000380756.7:c.1856del ENSP00000370132.3:p.Pro619LeufsTer?
ENST00000402667.1:c.1187del ENSP00000384237.1:p.Pro396LeufsTer?
ENST00000461228.1:n.5del
ENST00000474887.5:n.175del
NM_022552.4:c.1856del , LRG_459t1:c.1856del NP_072046.2:p.Pro619LeufsTer?
NM_153759.3:c.1289del , LRG_459t2:c.1289del NP_715640.2:p.Pro430LeufsTer?
NM_175629.2:c.1856del , LRG_459t4:c.1856del NP_783328.1:p.Pro619LeufsTer?
XM_005264175.3:c.1856del XP_005264232.1:p.Pro619LeufsTer?
XM_005264177.3:c.1187del XP_005264234.1:p.Pro396LeufsTer?
XM_006711957.2:c.1856del XP_006712020.1:p.Pro619LeufsTer?
XM_006711958.2:c.1412del XP_006712021.1:p.Pro471LeufsTer?
XM_011532662.1:c.1709del XP_011530964.1:p.Pro570LeufsTer?
XM_011532663.1:c.1691del XP_011530965.1:p.Pro564LeufsTer?
XM_011532664.1:c.1856del XP_011530966.1:p.Pro619LeufsTer?
XM_011532665.1:c.1400del XP_011530967.1:p.Pro467LeufsTer?
XM_011532666.1:c.1328del XP_011530968.1:p.Pro443LeufsTer?
XM_011532667.1:c.1187del XP_011530969.1:p.Pro396LeufsTer?
XM_011532668.1:c.1856del XP_011530970.1:p.Pro619LeufsTer?
NM_001320893.1:c.1400del NP_001307822.1:p.Pro467LeufsTer?
NR_135490.1:n.2194del
XM_005264175.5:c.1856del XP_005264232.1:p.Pro619LeufsTer?
XM_005264177.4:c.1187del XP_005264234.1:p.Pro396LeufsTer?
XM_011532662.2:c.1709del XP_011530964.1:p.Pro570LeufsTer?
XM_011532663.2:c.1691del XP_011530965.1:p.Pro564LeufsTer?
XM_011532664.2:c.1856del XP_011530966.1:p.Pro619LeufsTer?
XM_011532666.2:c.1328del XP_011530968.1:p.Pro443LeufsTer?
XM_011532667.3:c.1187del XP_011530969.1:p.Pro396LeufsTer?
XM_017003526.1:c.1856del XP_016859015.1:p.Pro619LeufsTer?
XM_017003527.1:c.1187del XP_016859016.1:p.Pro396LeufsTer?
XR_001738657.1:n.2133del
NM_001375819.1:c.1187del NP_001362748.1:p.Pro396LeufsTer?
NR_135490.2:n.2087del
NM_022552.5:c.1856del MANE Select NP_072046.2:p.Pro619LeufsTer?