Canonical Allele Identifier: CA1239260116

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234016G= , CM000664.2:g.25234016G=	GRCh38
NC_000002.11:g.25456885G= , CM000664.1:g.25456885G=	GRCh37
NC_000002.10:g.25310389G=	NCBI36
NG_029465.2:g.113575C= , LRG_459:g.113575C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.2148C=	ENSP00000508654.1:n.2148C=
ENST00000683760.1:c.*263C=	ENSP00000507765.1:n.*263C=
ENST00000321117.10:c.*263C= MANE Select	ENSP00000324375.5:n.*263C=
ENST00000264709.7:c.*263C=	ENSP00000264709.3:n.*263C=
ENST00000321117.9:c.*263C=	ENSP00000324375.5:n.*263C=
ENST00000380746.8:c.*263C=	ENSP00000370122.4:n.*263C=
ENST00000380756.7:c.*855C=	ENSP00000370132.3:n.*855C=
NM_022552.4:c.*263C= , LRG_459t1:c.*263C=	NP_072046.2:n.*263C=
NM_153759.3:c.*263C= , LRG_459t2:c.*263C=	NP_715640.2:n.*263C=
NM_175629.2:c.*263C= , LRG_459t4:c.*263C=	NP_783328.1:n.*263C=
XM_005264175.3:c.*263C=	XP_005264232.1:n.*263C=
XM_005264177.3:c.*263C=	XP_005264234.1:n.*263C=
XM_006711958.2:c.*263C=	XP_006712021.1:n.*263C=
XM_011532662.1:c.*263C=	XP_011530964.1:n.*263C=
XM_011532663.1:c.*263C=	XP_011530965.1:n.*263C=
XM_011532665.1:c.*263C=	XP_011530967.1:n.*263C=
XM_011532666.1:c.*263C=	XP_011530968.1:n.*263C=
XM_011532667.1:c.*263C=	XP_011530969.1:n.*263C=
NM_001320893.1:c.*263C=	NP_001307822.1:n.*263C=
NR_135490.1:n.3539C=
XM_005264175.5:c.*263C=	XP_005264232.1:n.*263C=
XM_005264177.4:c.*263C=	XP_005264234.1:n.*263C=
XM_011532662.2:c.*263C=	XP_011530964.1:n.*263C=
XM_011532663.2:c.*263C=	XP_011530965.1:n.*263C=
XM_011532666.2:c.*263C=	XP_011530968.1:n.*263C=
XM_011532667.3:c.*263C=	XP_011530969.1:n.*263C=
XM_017003526.1:c.*263C=	XP_016859015.1:n.*263C=
XM_017003527.1:c.*263C=	XP_016859016.1:n.*263C=
XR_001738657.1:n.3209C=
NM_001375819.1:c.*263C=	NP_001362748.1:n.*263C=
NR_135490.2:n.3432C=
NM_022552.5:c.*263C= MANE Select	NP_072046.2:n.*263C=