Canonical Allele Identifier: CA346075260

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25247713C>G , CM000664.2:g.25247713C>G	GRCh38
NC_000002.11:g.25470582C>G , CM000664.1:g.25470582C>G	GRCh37
NC_000002.10:g.25324086C>G	NCBI36
NG_029465.2:g.99878G>C , LRG_459:g.99878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683760.1:c.223G>C	ENSP00000507765.1:p.Gly75Arg
ENST00000321117.10:c.892G>C MANE Select	ENSP00000324375.5:p.Gly298Arg
ENST00000264709.7:c.892G>C	ENSP00000264709.3:p.Gly298Arg
ENST00000321117.9:c.892G>C	ENSP00000324375.5:p.Gly298Arg
ENST00000380746.8:c.325G>C	ENSP00000370122.4:p.Gly109Arg
ENST00000380756.7:c.892G>C	ENSP00000370132.3:p.Gly298Arg
ENST00000402667.1:c.223G>C	ENSP00000384237.1:p.Gly75Arg
ENST00000470983.5:n.339G>C
ENST00000474807.5:n.187G>C
ENST00000496570.1:n.425G>C
NM_022552.4:c.892G>C , LRG_459t1:c.892G>C	NP_072046.2:p.Gly298Arg
NM_153759.3:c.325G>C , LRG_459t2:c.325G>C	NP_715640.2:p.Gly109Arg
NM_175629.2:c.892G>C , LRG_459t4:c.892G>C	NP_783328.1:p.Gly298Arg
XM_005264175.3:c.892G>C	XP_005264232.1:p.Gly298Arg
XM_005264177.3:c.223G>C	XP_005264234.1:p.Gly75Arg
XM_006711957.2:c.892G>C	XP_006712020.1:p.Gly298Arg
XM_006711958.2:c.448G>C	XP_006712021.1:p.Gly150Arg
XM_011532662.1:c.745G>C	XP_011530964.1:p.Gly249Arg
XM_011532663.1:c.727G>C	XP_011530965.1:p.Gly243Arg
XM_011532664.1:c.892G>C	XP_011530966.1:p.Gly298Arg
XM_011532665.1:c.436G>C	XP_011530967.1:p.Gly146Arg
XM_011532666.1:c.364G>C	XP_011530968.1:p.Gly122Arg
XM_011532667.1:c.223G>C	XP_011530969.1:p.Gly75Arg
XM_011532668.1:c.892G>C	XP_011530970.1:p.Gly298Arg
NM_001320893.1:c.436G>C	NP_001307822.1:p.Gly146Arg
NR_135490.1:n.1230G>C
XM_005264175.5:c.892G>C	XP_005264232.1:p.Gly298Arg
XM_005264177.4:c.223G>C	XP_005264234.1:p.Gly75Arg
XM_011532662.2:c.745G>C	XP_011530964.1:p.Gly249Arg
XM_011532663.2:c.727G>C	XP_011530965.1:p.Gly243Arg
XM_011532664.2:c.892G>C	XP_011530966.1:p.Gly298Arg
XM_011532666.2:c.364G>C	XP_011530968.1:p.Gly122Arg
XM_011532667.3:c.223G>C	XP_011530969.1:p.Gly75Arg
XM_017003526.1:c.892G>C	XP_016859015.1:p.Gly298Arg
XM_017003527.1:c.223G>C	XP_016859016.1:p.Gly75Arg
XR_001738657.1:n.1169G>C
NM_001375819.1:c.223G>C	NP_001362748.1:p.Gly75Arg
NR_135490.2:n.1123G>C
NM_022552.5:c.892G>C MANE Select	NP_072046.2:p.Gly298Arg