Canonical Allele Identifier: CA346069784

Gene: DNMT3A

Linked Data

• COSMIC: COSM4383535 ; COSM4383536
• MyVariant Identifiers: chr2:g.25463209C>A (hg19) ; chr2:g.25240340C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240340C>A , CM000664.2:g.25240340C>A	GRCh38
NC_000002.11:g.25463209C>A , CM000664.1:g.25463209C>A	GRCh37
NC_000002.10:g.25316713C>A	NCBI36
NG_029465.2:g.107251G>T , LRG_459:g.107251G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.603G>T
ENST00000683393.1:c.1430G>T	ENSP00000508654.1:n.1430G>T
ENST00000683760.1:c.1615G>T	ENSP00000507765.1:p.Gly539Cys
ENST00000321117.10:c.2284G>T MANE Select	ENSP00000324375.5:p.Gly762Cys
ENST00000264709.7:c.2284G>T	ENSP00000264709.3:p.Gly762Cys
ENST00000321117.9:c.2284G>T	ENSP00000324375.5:p.Gly762Cys
ENST00000380746.8:c.1717G>T	ENSP00000370122.4:p.Gly573Cys
ENST00000380756.7:c.2284G>T	ENSP00000370132.3:p.Gly762Cys
ENST00000402667.1:c.1615G>T	ENSP00000384237.1:p.Gly539Cys
ENST00000461228.1:n.503G>T
ENST00000466601.5:n.656G>T
ENST00000474887.5:n.603G>T
ENST00000482935.5:n.284G>T
ENST00000491288.5:n.310+300G>T
NM_022552.4:c.2284G>T , LRG_459t1:c.2284G>T	NP_072046.2:p.Gly762Cys
NM_153759.3:c.1717G>T , LRG_459t2:c.1717G>T	NP_715640.2:p.Gly573Cys
NM_175629.2:c.2284G>T , LRG_459t4:c.2284G>T	NP_783328.1:p.Gly762Cys
XM_005264175.3:c.2284G>T	XP_005264232.1:p.Gly762Cys
XM_005264177.3:c.1615G>T	XP_005264234.1:p.Gly539Cys
XM_006711957.2:c.2284G>T	XP_006712020.1:p.Gly762Cys
XM_006711958.2:c.1840G>T	XP_006712021.1:p.Gly614Cys
XM_011532662.1:c.2137G>T	XP_011530964.1:p.Gly713Cys
XM_011532663.1:c.2119G>T	XP_011530965.1:p.Gly707Cys
XM_011532664.1:c.2284G>T	XP_011530966.1:p.Gly762Cys
XM_011532665.1:c.1828G>T	XP_011530967.1:p.Gly610Cys
XM_011532666.1:c.1756G>T	XP_011530968.1:p.Gly586Cys
XM_011532667.1:c.1615G>T	XP_011530969.1:p.Gly539Cys
XM_011532668.1:c.2284G>T	XP_011530970.1:p.Gly762Cys
NM_001320893.1:c.1828G>T	NP_001307822.1:p.Gly610Cys
NR_135490.1:n.2622G>T
XM_005264175.5:c.2284G>T	XP_005264232.1:p.Gly762Cys
XM_005264177.4:c.1615G>T	XP_005264234.1:p.Gly539Cys
XM_011532662.2:c.2137G>T	XP_011530964.1:p.Gly713Cys
XM_011532663.2:c.2119G>T	XP_011530965.1:p.Gly707Cys
XM_011532664.2:c.2284G>T	XP_011530966.1:p.Gly762Cys
XM_011532666.2:c.1756G>T	XP_011530968.1:p.Gly586Cys
XM_011532667.3:c.1615G>T	XP_011530969.1:p.Gly539Cys
XM_017003526.1:c.2284G>T	XP_016859015.1:p.Gly762Cys
XM_017003527.1:c.1615G>T	XP_016859016.1:p.Gly539Cys
XR_001738657.1:n.2561G>T
NM_001375819.1:c.1615G>T	NP_001362748.1:p.Gly539Cys
NR_135490.2:n.2515G>T
NM_022552.5:c.2284G>T MANE Select	NP_072046.2:p.Gly762Cys