Canonical Allele Identifier: CA1239266805

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25247713C= , CM000664.2:g.25247713C=	GRCh38
NC_000002.11:g.25470582C= , CM000664.1:g.25470582C=	GRCh37
NC_000002.10:g.25324086C=	NCBI36
NG_029465.2:g.99878G= , LRG_459:g.99878G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683760.1:c.223G=	ENSP00000507765.1:p.Gly75=
ENST00000321117.10:c.892G= MANE Select	ENSP00000324375.5:p.Gly298=
ENST00000264709.7:c.892G=	ENSP00000264709.3:p.Gly298=
ENST00000321117.9:c.892G=	ENSP00000324375.5:p.Gly298=
ENST00000380746.8:c.325G=	ENSP00000370122.4:p.Gly109=
ENST00000380756.7:c.892G=	ENSP00000370132.3:p.Gly298=
ENST00000402667.1:c.223G=	ENSP00000384237.1:p.Gly75=
ENST00000470983.5:n.339G=
ENST00000474807.5:n.187G=
ENST00000496570.1:n.425G=
NM_022552.4:c.892G= , LRG_459t1:c.892G=	NP_072046.2:p.Gly298=
NM_153759.3:c.325G= , LRG_459t2:c.325G=	NP_715640.2:p.Gly109=
NM_175629.2:c.892G= , LRG_459t4:c.892G=	NP_783328.1:p.Gly298=
XM_005264175.3:c.892G=	XP_005264232.1:p.Gly298=
XM_005264177.3:c.223G=	XP_005264234.1:p.Gly75=
XM_006711957.2:c.892G=	XP_006712020.1:p.Gly298=
XM_006711958.2:c.448G=	XP_006712021.1:p.Gly150=
XM_011532662.1:c.745G=	XP_011530964.1:p.Gly249=
XM_011532663.1:c.727G=	XP_011530965.1:p.Gly243=
XM_011532664.1:c.892G=	XP_011530966.1:p.Gly298=
XM_011532665.1:c.436G=	XP_011530967.1:p.Gly146=
XM_011532666.1:c.364G=	XP_011530968.1:p.Gly122=
XM_011532667.1:c.223G=	XP_011530969.1:p.Gly75=
XM_011532668.1:c.892G=	XP_011530970.1:p.Gly298=
NM_001320893.1:c.436G=	NP_001307822.1:p.Gly146=
NR_135490.1:n.1230G=
XM_005264175.5:c.892G=	XP_005264232.1:p.Gly298=
XM_005264177.4:c.223G=	XP_005264234.1:p.Gly75=
XM_011532662.2:c.745G=	XP_011530964.1:p.Gly249=
XM_011532663.2:c.727G=	XP_011530965.1:p.Gly243=
XM_011532664.2:c.892G=	XP_011530966.1:p.Gly298=
XM_011532666.2:c.364G=	XP_011530968.1:p.Gly122=
XM_011532667.3:c.223G=	XP_011530969.1:p.Gly75=
XM_017003526.1:c.892G=	XP_016859015.1:p.Gly298=
XM_017003527.1:c.223G=	XP_016859016.1:p.Gly75=
XR_001738657.1:n.1169G=
NM_001375819.1:c.223G=	NP_001362748.1:p.Gly75=
NR_135490.2:n.1123G=
NM_022552.5:c.892G= MANE Select	NP_072046.2:p.Gly298=