Canonical Allele Identifier: CA2576694246

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25243977del , CM000664.2:g.25243977del	GRCh38
NC_000002.11:g.25466846del , CM000664.1:g.25466846del	GRCh37
NC_000002.10:g.25320350del	NCBI36
NG_029465.2:g.103614del , LRG_459:g.103614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.176del
ENST00000683393.1:c.1003del	ENSP00000508654.1:n.1003del
ENST00000683760.1:c.1188del	ENSP00000507765.1:p.Pro397GlnfsTer?
ENST00000321117.10:c.1857del MANE Select	ENSP00000324375.5:p.Pro620GlnfsTer?
ENST00000264709.7:c.1857del	ENSP00000264709.3:p.Pro620GlnfsTer?
ENST00000321117.9:c.1857del	ENSP00000324375.5:p.Pro620GlnfsTer?
ENST00000380746.8:c.1290del	ENSP00000370122.4:p.Pro431GlnfsTer?
ENST00000380756.7:c.1857del	ENSP00000370132.3:p.Pro620GlnfsTer?
ENST00000402667.1:c.1188del	ENSP00000384237.1:p.Pro397GlnfsTer?
ENST00000461228.1:n.6del
ENST00000474887.5:n.176del
ENST00000482935.5:n.3del
NM_022552.4:c.1857del , LRG_459t1:c.1857del	NP_072046.2:p.Pro620GlnfsTer?
NM_153759.3:c.1290del , LRG_459t2:c.1290del	NP_715640.2:p.Pro431GlnfsTer?
NM_175629.2:c.1857del , LRG_459t4:c.1857del	NP_783328.1:p.Pro620GlnfsTer?
XM_005264175.3:c.1857del	XP_005264232.1:p.Pro620GlnfsTer?
XM_005264177.3:c.1188del	XP_005264234.1:p.Pro397GlnfsTer?
XM_006711957.2:c.1857del	XP_006712020.1:p.Pro620GlnfsTer?
XM_006711958.2:c.1413del	XP_006712021.1:p.Pro472GlnfsTer?
XM_011532662.1:c.1710del	XP_011530964.1:p.Pro571GlnfsTer?
XM_011532663.1:c.1692del	XP_011530965.1:p.Pro565GlnfsTer?
XM_011532664.1:c.1857del	XP_011530966.1:p.Pro620GlnfsTer?
XM_011532665.1:c.1401del	XP_011530967.1:p.Pro468GlnfsTer?
XM_011532666.1:c.1329del	XP_011530968.1:p.Pro444GlnfsTer?
XM_011532667.1:c.1188del	XP_011530969.1:p.Pro397GlnfsTer?
XM_011532668.1:c.1857del	XP_011530970.1:p.Pro620GlnfsTer?
NM_001320893.1:c.1401del	NP_001307822.1:p.Pro468GlnfsTer?
NR_135490.1:n.2195del
XM_005264175.5:c.1857del	XP_005264232.1:p.Pro620GlnfsTer?
XM_005264177.4:c.1188del	XP_005264234.1:p.Pro397GlnfsTer?
XM_011532662.2:c.1710del	XP_011530964.1:p.Pro571GlnfsTer?
XM_011532663.2:c.1692del	XP_011530965.1:p.Pro565GlnfsTer?
XM_011532664.2:c.1857del	XP_011530966.1:p.Pro620GlnfsTer?
XM_011532666.2:c.1329del	XP_011530968.1:p.Pro444GlnfsTer?
XM_011532667.3:c.1188del	XP_011530969.1:p.Pro397GlnfsTer?
XM_017003526.1:c.1857del	XP_016859015.1:p.Pro620GlnfsTer?
XM_017003527.1:c.1188del	XP_016859016.1:p.Pro397GlnfsTer?
XR_001738657.1:n.2134del
NM_001375819.1:c.1188del	NP_001362748.1:p.Pro397GlnfsTer?
NR_135490.2:n.2088del
NM_022552.5:c.1857del MANE Select	NP_072046.2:p.Pro620GlnfsTer?