Canonical Allele Identifier: CA1239266802

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25247710T= , CM000664.2:g.25247710T=	GRCh38
NC_000002.11:g.25470579T= , CM000664.1:g.25470579T=	GRCh37
NC_000002.10:g.25324083T=	NCBI36
NG_029465.2:g.99881A= , LRG_459:g.99881A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.1A=	ENSP00000508654.1:p.Lys1=
ENST00000683760.1:c.226A=	ENSP00000507765.1:p.Lys76=
ENST00000321117.10:c.895A= MANE Select	ENSP00000324375.5:p.Lys299=
ENST00000264709.7:c.895A=	ENSP00000264709.3:p.Lys299=
ENST00000321117.9:c.895A=	ENSP00000324375.5:p.Lys299=
ENST00000380746.8:c.328A=	ENSP00000370122.4:p.Lys110=
ENST00000380756.7:c.895A=	ENSP00000370132.3:p.Lys299=
ENST00000402667.1:c.226A=	ENSP00000384237.1:p.Lys76=
ENST00000470983.5:n.342A=
ENST00000474807.5:n.190A=
ENST00000496570.1:n.428A=
NM_022552.4:c.895A= , LRG_459t1:c.895A=	NP_072046.2:p.Lys299=
NM_153759.3:c.328A= , LRG_459t2:c.328A=	NP_715640.2:p.Lys110=
NM_175629.2:c.895A= , LRG_459t4:c.895A=	NP_783328.1:p.Lys299=
XM_005264175.3:c.895A=	XP_005264232.1:p.Lys299=
XM_005264177.3:c.226A=	XP_005264234.1:p.Lys76=
XM_006711957.2:c.895A=	XP_006712020.1:p.Lys299=
XM_006711958.2:c.451A=	XP_006712021.1:p.Lys151=
XM_011532662.1:c.748A=	XP_011530964.1:p.Lys250=
XM_011532663.1:c.730A=	XP_011530965.1:p.Lys244=
XM_011532664.1:c.895A=	XP_011530966.1:p.Lys299=
XM_011532665.1:c.439A=	XP_011530967.1:p.Lys147=
XM_011532666.1:c.367A=	XP_011530968.1:p.Lys123=
XM_011532667.1:c.226A=	XP_011530969.1:p.Lys76=
XM_011532668.1:c.895A=	XP_011530970.1:p.Lys299=
NM_001320893.1:c.439A=	NP_001307822.1:p.Lys147=
NR_135490.1:n.1233A=
XM_005264175.5:c.895A=	XP_005264232.1:p.Lys299=
XM_005264177.4:c.226A=	XP_005264234.1:p.Lys76=
XM_011532662.2:c.748A=	XP_011530964.1:p.Lys250=
XM_011532663.2:c.730A=	XP_011530965.1:p.Lys244=
XM_011532664.2:c.895A=	XP_011530966.1:p.Lys299=
XM_011532666.2:c.367A=	XP_011530968.1:p.Lys123=
XM_011532667.3:c.226A=	XP_011530969.1:p.Lys76=
XM_017003526.1:c.895A=	XP_016859015.1:p.Lys299=
XM_017003527.1:c.226A=	XP_016859016.1:p.Lys76=
XR_001738657.1:n.1172A=
NM_001375819.1:c.226A=	NP_001362748.1:p.Lys76=
NR_135490.2:n.1126A=
NM_022552.5:c.895A= MANE Select	NP_072046.2:p.Lys299=