Canonical Allele Identifier: CA1239262950

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244279A= , CM000664.2:g.25244279A=	GRCh38
NC_000002.11:g.25467148A= , CM000664.1:g.25467148A=	GRCh37
NC_000002.10:g.25320652A=	NCBI36
NG_029465.2:g.103312T= , LRG_459:g.103312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.46T=
ENST00000683393.1:c.873T=	ENSP00000508654.1:n.873T=
ENST00000683760.1:c.1058T=	ENSP00000507765.1:p.Ile353=
ENST00000321117.10:c.1727T= MANE Select	ENSP00000324375.5:p.Ile576=
ENST00000264709.7:c.1727T=	ENSP00000264709.3:p.Ile576=
ENST00000321117.9:c.1727T=	ENSP00000324375.5:p.Ile576=
ENST00000380746.8:c.1160T=	ENSP00000370122.4:p.Ile387=
ENST00000380756.7:c.1727T=	ENSP00000370132.3:p.Ile576=
ENST00000402667.1:c.1058T=	ENSP00000384237.1:p.Ile353=
ENST00000474887.5:n.46T=
NM_022552.4:c.1727T= , LRG_459t1:c.1727T=	NP_072046.2:p.Ile576=
NM_153759.3:c.1160T= , LRG_459t2:c.1160T=	NP_715640.2:p.Ile387=
NM_175629.2:c.1727T= , LRG_459t4:c.1727T=	NP_783328.1:p.Ile576=
XM_005264175.3:c.1727T=	XP_005264232.1:p.Ile576=
XM_005264177.3:c.1058T=	XP_005264234.1:p.Ile353=
XM_006711957.2:c.1727T=	XP_006712020.1:p.Ile576=
XM_006711958.2:c.1283T=	XP_006712021.1:p.Ile428=
XM_011532662.1:c.1580T=	XP_011530964.1:p.Ile527=
XM_011532663.1:c.1562T=	XP_011530965.1:p.Ile521=
XM_011532664.1:c.1727T=	XP_011530966.1:p.Ile576=
XM_011532665.1:c.1271T=	XP_011530967.1:p.Ile424=
XM_011532666.1:c.1199T=	XP_011530968.1:p.Ile400=
XM_011532667.1:c.1058T=	XP_011530969.1:p.Ile353=
XM_011532668.1:c.1727T=	XP_011530970.1:p.Ile576=
NM_001320893.1:c.1271T=	NP_001307822.1:p.Ile424=
NR_135490.1:n.2065T=
XM_005264175.5:c.1727T=	XP_005264232.1:p.Ile576=
XM_005264177.4:c.1058T=	XP_005264234.1:p.Ile353=
XM_011532662.2:c.1580T=	XP_011530964.1:p.Ile527=
XM_011532663.2:c.1562T=	XP_011530965.1:p.Ile521=
XM_011532664.2:c.1727T=	XP_011530966.1:p.Ile576=
XM_011532666.2:c.1199T=	XP_011530968.1:p.Ile400=
XM_011532667.3:c.1058T=	XP_011530969.1:p.Ile353=
XM_017003526.1:c.1727T=	XP_016859015.1:p.Ile576=
XM_017003527.1:c.1058T=	XP_016859016.1:p.Ile353=
XR_001738657.1:n.2004T=
NM_001375819.1:c.1058T=	NP_001362748.1:p.Ile353=
NR_135490.2:n.1958T=
NM_022552.5:c.1727T= MANE Select	NP_072046.2:p.Ile576=