Canonical Allele Identifier: CA346083673

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25282462G>A , CM000664.2:g.25282462G>A	GRCh38
NC_000002.11:g.25505331G>A , CM000664.1:g.25505331G>A	GRCh37
NC_000002.10:g.25358835G>A	NCBI36
NG_029465.2:g.65129C>T , LRG_459:g.65129C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.427C>T MANE Select	NP_072046.2:p.Arg143Ter
ENST00000321117.10:c.427C>T MANE Select	ENSP00000324375.5:p.Arg143Ter
NM_001320892.1:c.427C>T	NP_001307821.1:p.Arg143Ter
NM_001320892.2:c.427C>T	NP_001307821.1:p.Arg143Ter
NM_022552.4:c.427C>T , LRG_459t1:c.427C>T	NP_072046.2:p.Arg143Ter
NM_175629.2:c.427C>T , LRG_459t4:c.427C>T	NP_783328.1:p.Arg143Ter
NM_175630.1:c.427C>T , LRG_459t3:c.427C>T	NP_783329.1:p.Arg143Ter
NR_135490.1:n.765C>T
NR_135490.2:n.658C>T
ENST00000264709.7:c.427C>T	ENSP00000264709.3:p.Arg143Ter
ENST00000321117.9:c.427C>T	ENSP00000324375.5:p.Arg143Ter
ENST00000380756.7:c.427C>T	ENSP00000370132.3:p.Arg143Ter
ENST00000406659.3:c.427C>T	ENSP00000384852.3:p.Arg143Ter
XM_005264175.3:c.427C>T	XP_005264232.1:p.Arg143Ter
XM_005264175.5:c.427C>T	XP_005264232.1:p.Arg143Ter
XM_006711957.2:c.427C>T	XP_006712020.1:p.Arg143Ter
XM_011532662.1:c.280C>T	XP_011530964.1:p.Arg94Ter
XM_011532662.2:c.280C>T	XP_011530964.1:p.Arg94Ter
XM_011532663.1:c.159C>T	XP_011530965.1:p.Ala53=
XM_011532663.2:c.159C>T	XP_011530965.1:p.Ala53=
XM_011532664.1:c.427C>T	XP_011530966.1:p.Arg143Ter
XM_011532664.2:c.427C>T	XP_011530966.1:p.Arg143Ter
XM_011532668.1:c.427C>T	XP_011530970.1:p.Arg143Ter
XM_017003526.1:c.427C>T	XP_016859015.1:p.Arg143Ter
XR_001738657.1:n.704C>T