Canonical Allele Identifier: CA346251793

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25300240C>G , CM000664.2:g.25300240C>G	GRCh38
NC_000002.11:g.25523109C>G , CM000664.1:g.25523109C>G	GRCh37
NC_000002.10:g.25376613C>G	NCBI36
NG_029465.2:g.47351G>C , LRG_459:g.47351G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.76G>C MANE Select	NP_072046.2:p.Gly26Arg
ENST00000321117.10:c.76G>C MANE Select	ENSP00000324375.5:p.Gly26Arg
NM_001320892.1:c.76G>C	NP_001307821.1:p.Gly26Arg
NM_001320892.2:c.76G>C	NP_001307821.1:p.Gly26Arg
NM_022552.4:c.76G>C , LRG_459t1:c.76G>C	NP_072046.2:p.Gly26Arg
NM_175629.2:c.76G>C , LRG_459t4:c.76G>C	NP_783328.1:p.Gly26Arg
NM_175630.1:c.76G>C , LRG_459t3:c.76G>C	NP_783329.1:p.Gly26Arg
NR_135490.1:n.414G>C
NR_135490.2:n.307G>C
ENST00000264709.7:c.76G>C	ENSP00000264709.3:p.Gly26Arg
ENST00000321117.9:c.76G>C	ENSP00000324375.5:p.Gly26Arg
ENST00000380756.7:c.76G>C	ENSP00000370132.3:p.Gly26Arg
ENST00000406659.3:c.76G>C	ENSP00000384852.3:p.Gly26Arg
XM_005264175.3:c.76G>C	XP_005264232.1:p.Gly26Arg
XM_005264175.5:c.76G>C	XP_005264232.1:p.Gly26Arg
XM_006711957.2:c.76G>C	XP_006712020.1:p.Gly26Arg
XM_011532663.1:c.-193G>C	XP_011530965.1:n.-193G>C
XM_011532663.2:c.-193G>C	XP_011530965.1:n.-193G>C
XM_011532664.1:c.76G>C	XP_011530966.1:p.Gly26Arg
XM_011532664.2:c.76G>C	XP_011530966.1:p.Gly26Arg
XM_011532668.1:c.76G>C	XP_011530970.1:p.Gly26Arg
XM_017003526.1:c.76G>C	XP_016859015.1:p.Gly26Arg
XR_001738657.1:n.353G>C