Canonical Allele Identifier: CA2658171770

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25240312-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240313del , CM000664.2:g.25240313del	GRCh38
NC_000002.11:g.25463182del , CM000664.1:g.25463182del	GRCh37
NC_000002.10:g.25316686del	NCBI36
NG_029465.2:g.107278del , LRG_459:g.107278del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.630del
ENST00000683393.1:c.1457del	ENSP00000508654.1:n.1457del
ENST00000683760.1:c.1642del	ENSP00000507765.1:p.Arg548AspfsTer8
ENST00000321117.10:c.2311del MANE Select	ENSP00000324375.5:p.Arg771AspfsTer8
ENST00000264709.7:c.2311del	ENSP00000264709.3:p.Arg771AspfsTer8
ENST00000321117.9:c.2311del	ENSP00000324375.5:p.Arg771AspfsTer8
ENST00000380746.8:c.1744del	ENSP00000370122.4:p.Arg582AspfsTer8
ENST00000380756.7:c.2311del	ENSP00000370132.3:p.Arg771AspfsTer?
ENST00000402667.1:c.1642del	ENSP00000384237.1:p.Arg548AspfsTer8
ENST00000461228.1:n.530del
ENST00000466601.5:n.683del
ENST00000474887.5:n.630del
ENST00000482935.5:n.311del
ENST00000491288.5:n.310+327del
NM_022552.4:c.2311del , LRG_459t1:c.2311del	NP_072046.2:p.Arg771AspfsTer8
NM_153759.3:c.1744del , LRG_459t2:c.1744del	NP_715640.2:p.Arg582AspfsTer8
NM_175629.2:c.2311del , LRG_459t4:c.2311del	NP_783328.1:p.Arg771AspfsTer8
XM_005264175.3:c.2311del	XP_005264232.1:p.Arg771AspfsTer8
XM_005264177.3:c.1642del	XP_005264234.1:p.Arg548AspfsTer8
XM_006711957.2:c.2311del	XP_006712020.1:p.Arg771AspfsTer8
XM_006711958.2:c.1867del	XP_006712021.1:p.Arg623AspfsTer8
XM_011532662.1:c.2164del	XP_011530964.1:p.Arg722AspfsTer8
XM_011532663.1:c.2146del	XP_011530965.1:p.Arg716AspfsTer8
XM_011532664.1:c.2311del	XP_011530966.1:p.Arg771AspfsTer?
XM_011532665.1:c.1855del	XP_011530967.1:p.Arg619AspfsTer8
XM_011532666.1:c.1783del	XP_011530968.1:p.Arg595AspfsTer8
XM_011532667.1:c.1642del	XP_011530969.1:p.Arg548AspfsTer8
XM_011532668.1:c.2311del	XP_011530970.1:p.Arg771AspfsTer?
NM_001320893.1:c.1855del	NP_001307822.1:p.Arg619AspfsTer8
NR_135490.1:n.2649del
XM_005264175.5:c.2311del	XP_005264232.1:p.Arg771AspfsTer8
XM_005264177.4:c.1642del	XP_005264234.1:p.Arg548AspfsTer8
XM_011532662.2:c.2164del	XP_011530964.1:p.Arg722AspfsTer8
XM_011532663.2:c.2146del	XP_011530965.1:p.Arg716AspfsTer8
XM_011532664.2:c.2311del	XP_011530966.1:p.Arg771AspfsTer?
XM_011532666.2:c.1783del	XP_011530968.1:p.Arg595AspfsTer8
XM_011532667.3:c.1642del	XP_011530969.1:p.Arg548AspfsTer8
XM_017003526.1:c.2311del	XP_016859015.1:p.Arg771AspfsTer8
XM_017003527.1:c.1642del	XP_016859016.1:p.Arg548AspfsTer8
XR_001738657.1:n.2588del
NM_001375819.1:c.1642del	NP_001362748.1:p.Arg548AspfsTer8
NR_135490.2:n.2542del
NM_022552.5:c.2311del MANE Select	NP_072046.2:p.Arg771AspfsTer8