Canonical Allele Identifier: CA1239260244

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234299C= , CM000664.2:g.25234299C=	GRCh38
NC_000002.11:g.25457168C= , CM000664.1:g.25457168C=	GRCh37
NC_000002.10:g.25310672C=	NCBI36
NG_029465.2:g.113292G= , LRG_459:g.113292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.968G=
ENST00000683393.1:c.1865G=	ENSP00000508654.1:n.1865G=
ENST00000683760.1:c.2050G=	ENSP00000507765.1:p.Glu684=
ENST00000321117.10:c.2719G= MANE Select	ENSP00000324375.5:p.Glu907=
ENST00000264709.7:c.2719G=	ENSP00000264709.3:p.Glu907=
ENST00000321117.9:c.2719G=	ENSP00000324375.5:p.Glu907=
ENST00000380746.8:c.2152G=	ENSP00000370122.4:p.Glu718=
ENST00000380756.7:c.*572G=	ENSP00000370132.3:n.*572G=
ENST00000402667.1:c.2050G=	ENSP00000384237.1:p.Glu684=
NM_022552.4:c.2719G= , LRG_459t1:c.2719G=	NP_072046.2:p.Glu907=
NM_153759.3:c.2152G= , LRG_459t2:c.2152G=	NP_715640.2:p.Glu718=
NM_175629.2:c.2719G= , LRG_459t4:c.2719G=	NP_783328.1:p.Glu907=
XM_005264175.3:c.2719G=	XP_005264232.1:p.Glu907=
XM_005264177.3:c.2050G=	XP_005264234.1:p.Glu684=
XM_006711958.2:c.2275G=	XP_006712021.1:p.Glu759=
XM_011532662.1:c.2572G=	XP_011530964.1:p.Glu858=
XM_011532663.1:c.2554G=	XP_011530965.1:p.Glu852=
XM_011532665.1:c.2263G=	XP_011530967.1:p.Glu755=
XM_011532666.1:c.2191G=	XP_011530968.1:p.Glu731=
XM_011532667.1:c.2050G=	XP_011530969.1:p.Glu684=
NM_001320893.1:c.2263G=	NP_001307822.1:p.Glu755=
NR_135490.1:n.3256G=
XM_005264175.5:c.2719G=	XP_005264232.1:p.Glu907=
XM_005264177.4:c.2050G=	XP_005264234.1:p.Glu684=
XM_011532662.2:c.2572G=	XP_011530964.1:p.Glu858=
XM_011532663.2:c.2554G=	XP_011530965.1:p.Glu852=
XM_011532666.2:c.2191G=	XP_011530968.1:p.Glu731=
XM_011532667.3:c.2050G=	XP_011530969.1:p.Glu684=
XM_017003526.1:c.2719G=	XP_016859015.1:p.Glu907=
XM_017003527.1:c.2050G=	XP_016859016.1:p.Glu684=
XR_001738657.1:n.2926G=
NM_001375819.1:c.2050G=	NP_001362748.1:p.Glu684=
NR_135490.2:n.3149G=
NM_022552.5:c.2719G= MANE Select	NP_072046.2:p.Glu907=