Canonical Allele Identifier: CA1239279312

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25275414A= , CM000664.2:g.25275414A=	GRCh38
NC_000002.11:g.25498283A= , CM000664.1:g.25498283A=	GRCh37
NC_000002.10:g.25351787A=	NCBI36
NG_029465.2:g.72177T= , LRG_459:g.72177T=

Transcript Alleles

HGVS	Amino-acid Change
NM_022552.5:c.492+86T= MANE Select	NP_072046.2:n.492+86T=
ENST00000321117.10:c.492+86T= MANE Select	ENSP00000324375.5:n.492+86T=
NM_022552.4:c.492+86T= , LRG_459t1:c.492+86T=	NP_072046.2:n.492+86T=
NM_175629.2:c.492+86T= , LRG_459t4:c.492+86T=	NP_783328.1:n.492+86T=
NR_135490.1:n.830+86T=
NR_135490.2:n.723+86T=
ENST00000264709.7:c.492+86T=	ENSP00000264709.3:n.492+86T=
ENST00000321117.9:c.492+86T=	ENSP00000324375.5:n.492+86T=
ENST00000380756.7:c.492+86T=	ENSP00000370132.3:n.492+86T=
ENST00000682842.1:n.21+86T=
XM_005264175.3:c.492+86T=	XP_005264232.1:n.492+86T=
XM_005264175.5:c.492+86T=	XP_005264232.1:n.492+86T=
XM_006711957.2:c.492+86T=	XP_006712020.1:n.492+86T=
XM_006711958.2:c.48+86T=	XP_006712021.1:n.48+86T=
XM_011532662.1:c.345+86T=	XP_011530964.1:n.345+86T=
XM_011532662.2:c.345+86T=	XP_011530964.1:n.345+86T=
XM_011532663.1:c.327+86T=	XP_011530965.1:n.327+86T=
XM_011532663.2:c.327+86T=	XP_011530965.1:n.327+86T=
XM_011532664.1:c.492+86T=	XP_011530966.1:n.492+86T=
XM_011532664.2:c.492+86T=	XP_011530966.1:n.492+86T=
XM_011532668.1:c.492+86T=	XP_011530970.1:n.492+86T=
XM_017003526.1:c.492+86T=	XP_016859015.1:n.492+86T=
XR_001738657.1:n.769+86T=