Canonical Allele Identifier: CA346068215

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1553408402
• MyVariant Identifiers: chr2:g.25457260T>A (hg19) ; chr2:g.25234391T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234391T>A , CM000664.2:g.25234391T>A	GRCh38
NC_000002.11:g.25457260T>A , CM000664.1:g.25457260T>A	GRCh37
NC_000002.10:g.25310764T>A	NCBI36
NG_029465.2:g.113200A>T , LRG_459:g.113200A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.876A>T
ENST00000683393.1:c.1773A>T	ENSP00000508654.1:n.1773A>T
ENST00000683760.1:c.1958A>T	ENSP00000507765.1:p.Asp653Val
ENST00000321117.10:c.2627A>T MANE Select	ENSP00000324375.5:p.Asp876Val
ENST00000264709.7:c.2627A>T	ENSP00000264709.3:p.Asp876Val
ENST00000321117.9:c.2627A>T	ENSP00000324375.5:p.Asp876Val
ENST00000380746.8:c.2060A>T	ENSP00000370122.4:p.Asp687Val
ENST00000380756.7:c.*480A>T	ENSP00000370132.3:n.*480A>T
ENST00000402667.1:c.1958A>T	ENSP00000384237.1:p.Asp653Val
NM_022552.4:c.2627A>T , LRG_459t1:c.2627A>T	NP_072046.2:p.Asp876Val
NM_153759.3:c.2060A>T , LRG_459t2:c.2060A>T	NP_715640.2:p.Asp687Val
NM_175629.2:c.2627A>T , LRG_459t4:c.2627A>T	NP_783328.1:p.Asp876Val
XM_005264175.3:c.2627A>T	XP_005264232.1:p.Asp876Val
XM_005264177.3:c.1958A>T	XP_005264234.1:p.Asp653Val
XM_006711958.2:c.2183A>T	XP_006712021.1:p.Asp728Val
XM_011532662.1:c.2480A>T	XP_011530964.1:p.Asp827Val
XM_011532663.1:c.2462A>T	XP_011530965.1:p.Asp821Val
XM_011532665.1:c.2171A>T	XP_011530967.1:p.Asp724Val
XM_011532666.1:c.2099A>T	XP_011530968.1:p.Asp700Val
XM_011532667.1:c.1958A>T	XP_011530969.1:p.Asp653Val
NM_001320893.1:c.2171A>T	NP_001307822.1:p.Asp724Val
NR_135490.1:n.3164A>T
XM_005264175.5:c.2627A>T	XP_005264232.1:p.Asp876Val
XM_005264177.4:c.1958A>T	XP_005264234.1:p.Asp653Val
XM_011532662.2:c.2480A>T	XP_011530964.1:p.Asp827Val
XM_011532663.2:c.2462A>T	XP_011530965.1:p.Asp821Val
XM_011532666.2:c.2099A>T	XP_011530968.1:p.Asp700Val
XM_011532667.3:c.1958A>T	XP_011530969.1:p.Asp653Val
XM_017003526.1:c.2627A>T	XP_016859015.1:p.Asp876Val
XM_017003527.1:c.1958A>T	XP_016859016.1:p.Asp653Val
XR_001738657.1:n.2834A>T
NM_001375819.1:c.1958A>T	NP_001362748.1:p.Asp653Val
NR_135490.2:n.3057A>T
NM_022552.5:c.2627A>T MANE Select	NP_072046.2:p.Asp876Val