Canonical Allele Identifier: CA1239254506

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234347G= , CM000664.2:g.25234347G=	GRCh38
NC_000002.11:g.25457216G= , CM000664.1:g.25457216G=	GRCh37
NC_000002.10:g.25310720G=	NCBI36
NG_029465.2:g.113244C= , LRG_459:g.113244C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.920C=
ENST00000683393.1:c.1817C=	ENSP00000508654.1:n.1817C=
ENST00000683760.1:c.2002C=	ENSP00000507765.1:p.Arg668=
ENST00000321117.10:c.2671C= MANE Select	ENSP00000324375.5:p.Arg891=
ENST00000264709.7:c.2671C=	ENSP00000264709.3:p.Arg891=
ENST00000321117.9:c.2671C=	ENSP00000324375.5:p.Arg891=
ENST00000380746.8:c.2104C=	ENSP00000370122.4:p.Arg702=
ENST00000380756.7:c.*524C=	ENSP00000370132.3:n.*524C=
ENST00000402667.1:c.2002C=	ENSP00000384237.1:p.Arg668=
NM_022552.4:c.2671C= , LRG_459t1:c.2671C=	NP_072046.2:p.Arg891=
NM_153759.3:c.2104C= , LRG_459t2:c.2104C=	NP_715640.2:p.Arg702=
NM_175629.2:c.2671C= , LRG_459t4:c.2671C=	NP_783328.1:p.Arg891=
XM_005264175.3:c.2671C=	XP_005264232.1:p.Arg891=
XM_005264177.3:c.2002C=	XP_005264234.1:p.Arg668=
XM_006711958.2:c.2227C=	XP_006712021.1:p.Arg743=
XM_011532662.1:c.2524C=	XP_011530964.1:p.Arg842=
XM_011532663.1:c.2506C=	XP_011530965.1:p.Arg836=
XM_011532665.1:c.2215C=	XP_011530967.1:p.Arg739=
XM_011532666.1:c.2143C=	XP_011530968.1:p.Arg715=
XM_011532667.1:c.2002C=	XP_011530969.1:p.Arg668=
NM_001320893.1:c.2215C=	NP_001307822.1:p.Arg739=
NR_135490.1:n.3208C=
XM_005264175.5:c.2671C=	XP_005264232.1:p.Arg891=
XM_005264177.4:c.2002C=	XP_005264234.1:p.Arg668=
XM_011532662.2:c.2524C=	XP_011530964.1:p.Arg842=
XM_011532663.2:c.2506C=	XP_011530965.1:p.Arg836=
XM_011532666.2:c.2143C=	XP_011530968.1:p.Arg715=
XM_011532667.3:c.2002C=	XP_011530969.1:p.Arg668=
XM_017003526.1:c.2671C=	XP_016859015.1:p.Arg891=
XM_017003527.1:c.2002C=	XP_016859016.1:p.Arg668=
XR_001738657.1:n.2878C=
NM_001375819.1:c.2002C=	NP_001362748.1:p.Arg668=
NR_135490.2:n.3101C=
NM_022552.5:c.2671C= MANE Select	NP_072046.2:p.Arg891=