Canonical Allele Identifier: CA346071659

Gene: DNMT3A

Linked Data

• dbSNP Id: rs1674428572
• gnomAD v3: 2-25244162-T-C
• gnomAD v4: 2-25244162-T-C
• MyVariant Identifiers: chr2:g.25467031T>C (hg19) ; chr2:g.25244162T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244162T>C , CM000664.2:g.25244162T>C	GRCh38
NC_000002.11:g.25467031T>C , CM000664.1:g.25467031T>C	GRCh37
NC_000002.10:g.25320535T>C	NCBI36
NG_029465.2:g.103429A>G , LRG_459:g.103429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.163A>G
ENST00000683393.1:c.990A>G	ENSP00000508654.1:n.990A>G
ENST00000683760.1:c.1175A>G	ENSP00000507765.1:p.Gln392Arg
ENST00000321117.10:c.1844A>G MANE Select	ENSP00000324375.5:p.Gln615Arg
ENST00000264709.7:c.1844A>G	ENSP00000264709.3:p.Gln615Arg
ENST00000321117.9:c.1844A>G	ENSP00000324375.5:p.Gln615Arg
ENST00000380746.8:c.1277A>G	ENSP00000370122.4:p.Gln426Arg
ENST00000380756.7:c.1844A>G	ENSP00000370132.3:p.Gln615Arg
ENST00000402667.1:c.1175A>G	ENSP00000384237.1:p.Gln392Arg
ENST00000474887.5:n.163A>G
NM_022552.4:c.1844A>G , LRG_459t1:c.1844A>G	NP_072046.2:p.Gln615Arg
NM_153759.3:c.1277A>G , LRG_459t2:c.1277A>G	NP_715640.2:p.Gln426Arg
NM_175629.2:c.1844A>G , LRG_459t4:c.1844A>G	NP_783328.1:p.Gln615Arg
XM_005264175.3:c.1844A>G	XP_005264232.1:p.Gln615Arg
XM_005264177.3:c.1175A>G	XP_005264234.1:p.Gln392Arg
XM_006711957.2:c.1844A>G	XP_006712020.1:p.Gln615Arg
XM_006711958.2:c.1400A>G	XP_006712021.1:p.Gln467Arg
XM_011532662.1:c.1697A>G	XP_011530964.1:p.Gln566Arg
XM_011532663.1:c.1679A>G	XP_011530965.1:p.Gln560Arg
XM_011532664.1:c.1844A>G	XP_011530966.1:p.Gln615Arg
XM_011532665.1:c.1388A>G	XP_011530967.1:p.Gln463Arg
XM_011532666.1:c.1316A>G	XP_011530968.1:p.Gln439Arg
XM_011532667.1:c.1175A>G	XP_011530969.1:p.Gln392Arg
XM_011532668.1:c.1844A>G	XP_011530970.1:p.Gln615Arg
NM_001320893.1:c.1388A>G	NP_001307822.1:p.Gln463Arg
NR_135490.1:n.2182A>G
XM_005264175.5:c.1844A>G	XP_005264232.1:p.Gln615Arg
XM_005264177.4:c.1175A>G	XP_005264234.1:p.Gln392Arg
XM_011532662.2:c.1697A>G	XP_011530964.1:p.Gln566Arg
XM_011532663.2:c.1679A>G	XP_011530965.1:p.Gln560Arg
XM_011532664.2:c.1844A>G	XP_011530966.1:p.Gln615Arg
XM_011532666.2:c.1316A>G	XP_011530968.1:p.Gln439Arg
XM_011532667.3:c.1175A>G	XP_011530969.1:p.Gln392Arg
XM_017003526.1:c.1844A>G	XP_016859015.1:p.Gln615Arg
XM_017003527.1:c.1175A>G	XP_016859016.1:p.Gln392Arg
XR_001738657.1:n.2121A>G
NM_001375819.1:c.1175A>G	NP_001362748.1:p.Gln392Arg
NR_135490.2:n.2075A>G
NM_022552.5:c.1844A>G MANE Select	NP_072046.2:p.Gln615Arg