Canonical Allele Identifier: CA425181407

Gene: DNMT3A

Linked Data

• COSMIC: COSM1583113
• MyVariant Identifiers: chr2:g.25463191del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240324del , CM000664.2:g.25240324del	GRCh38
NC_000002.11:g.25463193del , CM000664.1:g.25463193del	GRCh37
NC_000002.10:g.25316697del	NCBI36
NG_029465.2:g.107269del , LRG_459:g.107269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.621del
ENST00000683393.1:c.1448del	ENSP00000508654.1:n.1448del
ENST00000683760.1:c.1633del	ENSP00000507765.1:p.Asp545ThrfsTer11
ENST00000321117.10:c.2302del MANE Select	ENSP00000324375.5:p.Asp768ThrfsTer11
ENST00000264709.7:c.2302del	ENSP00000264709.3:p.Asp768ThrfsTer11
ENST00000321117.9:c.2302del	ENSP00000324375.5:p.Asp768ThrfsTer11
ENST00000380746.8:c.1735del	ENSP00000370122.4:p.Asp579ThrfsTer11
ENST00000380756.7:c.2302del	ENSP00000370132.3:p.Asp768ThrfsTer?
ENST00000402667.1:c.1633del	ENSP00000384237.1:p.Asp545ThrfsTer11
ENST00000461228.1:n.521del
ENST00000466601.5:n.674del
ENST00000474887.5:n.621del
ENST00000482935.5:n.302del
ENST00000491288.5:n.310+318del
NM_022552.4:c.2302del , LRG_459t1:c.2302del	NP_072046.2:p.Asp768ThrfsTer11
NM_153759.3:c.1735del , LRG_459t2:c.1735del	NP_715640.2:p.Asp579ThrfsTer11
NM_175629.2:c.2302del , LRG_459t4:c.2302del	NP_783328.1:p.Asp768ThrfsTer11
XM_005264175.3:c.2302del	XP_005264232.1:p.Asp768ThrfsTer11
XM_005264177.3:c.1633del	XP_005264234.1:p.Asp545ThrfsTer11
XM_006711957.2:c.2302del	XP_006712020.1:p.Asp768ThrfsTer11
XM_006711958.2:c.1858del	XP_006712021.1:p.Asp620ThrfsTer11
XM_011532662.1:c.2155del	XP_011530964.1:p.Asp719ThrfsTer11
XM_011532663.1:c.2137del	XP_011530965.1:p.Asp713ThrfsTer11
XM_011532664.1:c.2302del	XP_011530966.1:p.Asp768ThrfsTer?
XM_011532665.1:c.1846del	XP_011530967.1:p.Asp616ThrfsTer11
XM_011532666.1:c.1774del	XP_011530968.1:p.Asp592ThrfsTer11
XM_011532667.1:c.1633del	XP_011530969.1:p.Asp545ThrfsTer11
XM_011532668.1:c.2302del	XP_011530970.1:p.Asp768ThrfsTer?
NM_001320893.1:c.1846del	NP_001307822.1:p.Asp616ThrfsTer11
NR_135490.1:n.2640del
XM_005264175.5:c.2302del	XP_005264232.1:p.Asp768ThrfsTer11
XM_005264177.4:c.1633del	XP_005264234.1:p.Asp545ThrfsTer11
XM_011532662.2:c.2155del	XP_011530964.1:p.Asp719ThrfsTer11
XM_011532663.2:c.2137del	XP_011530965.1:p.Asp713ThrfsTer11
XM_011532664.2:c.2302del	XP_011530966.1:p.Asp768ThrfsTer?
XM_011532666.2:c.1774del	XP_011530968.1:p.Asp592ThrfsTer11
XM_011532667.3:c.1633del	XP_011530969.1:p.Asp545ThrfsTer11
XM_017003526.1:c.2302del	XP_016859015.1:p.Asp768ThrfsTer11
XM_017003527.1:c.1633del	XP_016859016.1:p.Asp545ThrfsTer11
XR_001738657.1:n.2579del
NM_001375819.1:c.1633del	NP_001362748.1:p.Asp545ThrfsTer11
NR_135490.2:n.2533del
NM_022552.5:c.2302del MANE Select	NP_072046.2:p.Asp768ThrfsTer11