Canonical Allele Identifier: CA916494387

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1558658644
• gnomAD v4: 2-25240313-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240314dup , CM000664.2:g.25240314dup	GRCh38
NC_000002.11:g.25463183dup , CM000664.1:g.25463183dup	GRCh37
NC_000002.10:g.25316687dup	NCBI36
NG_029465.2:g.107277dup , LRG_459:g.107277dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.629dup
ENST00000683393.1:c.1456dup	ENSP00000508654.1:n.1456dup
ENST00000683760.1:c.1641dup	ENSP00000507765.1:p.Arg548AlafsTer11
ENST00000321117.10:c.2310dup MANE Select	ENSP00000324375.5:p.Arg771AlafsTer11
ENST00000264709.7:c.2310dup	ENSP00000264709.3:p.Arg771AlafsTer11
ENST00000321117.9:c.2310dup	ENSP00000324375.5:p.Arg771AlafsTer11
ENST00000380746.8:c.1743dup	ENSP00000370122.4:p.Arg582AlafsTer11
ENST00000380756.7:c.2310dup	ENSP00000370132.3:p.Arg771AlafsTer8
ENST00000402667.1:c.1641dup	ENSP00000384237.1:p.Arg548AlafsTer11
ENST00000461228.1:n.529dup
ENST00000466601.5:n.682dup
ENST00000474887.5:n.629dup
ENST00000482935.5:n.310dup
ENST00000491288.5:n.310+326dup
NM_022552.4:c.2310dup , LRG_459t1:c.2310dup	NP_072046.2:p.Arg771AlafsTer11
NM_153759.3:c.1743dup , LRG_459t2:c.1743dup	NP_715640.2:p.Arg582AlafsTer11
NM_175629.2:c.2310dup , LRG_459t4:c.2310dup	NP_783328.1:p.Arg771AlafsTer11
XM_005264175.3:c.2310dup	XP_005264232.1:p.Arg771AlafsTer11
XM_005264177.3:c.1641dup	XP_005264234.1:p.Arg548AlafsTer11
XM_006711957.2:c.2310dup	XP_006712020.1:p.Arg771AlafsTer11
XM_006711958.2:c.1866dup	XP_006712021.1:p.Arg623AlafsTer11
XM_011532662.1:c.2163dup	XP_011530964.1:p.Arg722AlafsTer11
XM_011532663.1:c.2145dup	XP_011530965.1:p.Arg716AlafsTer11
XM_011532664.1:c.2310dup	XP_011530966.1:p.Arg771AlafsTer8
XM_011532665.1:c.1854dup	XP_011530967.1:p.Arg619AlafsTer11
XM_011532666.1:c.1782dup	XP_011530968.1:p.Arg595AlafsTer11
XM_011532667.1:c.1641dup	XP_011530969.1:p.Arg548AlafsTer11
XM_011532668.1:c.2310dup	XP_011530970.1:p.Arg771AlafsTer8
NM_001320893.1:c.1854dup	NP_001307822.1:p.Arg619AlafsTer11
NR_135490.1:n.2648dup
XM_005264175.5:c.2310dup	XP_005264232.1:p.Arg771AlafsTer11
XM_005264177.4:c.1641dup	XP_005264234.1:p.Arg548AlafsTer11
XM_011532662.2:c.2163dup	XP_011530964.1:p.Arg722AlafsTer11
XM_011532663.2:c.2145dup	XP_011530965.1:p.Arg716AlafsTer11
XM_011532664.2:c.2310dup	XP_011530966.1:p.Arg771AlafsTer8
XM_011532666.2:c.1782dup	XP_011530968.1:p.Arg595AlafsTer11
XM_011532667.3:c.1641dup	XP_011530969.1:p.Arg548AlafsTer11
XM_017003526.1:c.2310dup	XP_016859015.1:p.Arg771AlafsTer11
XM_017003527.1:c.1641dup	XP_016859016.1:p.Arg548AlafsTer11
XR_001738657.1:n.2587dup
NM_001375819.1:c.1641dup	NP_001362748.1:p.Arg548AlafsTer11
NR_135490.2:n.2541dup
NM_022552.5:c.2310dup MANE Select	NP_072046.2:p.Arg771AlafsTer11