Canonical Allele Identifier: CA1239262733

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244185C= , CM000664.2:g.25244185C=	GRCh38
NC_000002.11:g.25467054C= , CM000664.1:g.25467054C=	GRCh37
NC_000002.10:g.25320558C=	NCBI36
NG_029465.2:g.103406G= , LRG_459:g.103406G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.140G=
ENST00000683393.1:c.967G=	ENSP00000508654.1:n.967G=
ENST00000683760.1:c.1152G=	ENSP00000507765.1:p.Met384=
ENST00000321117.10:c.1821G= MANE Select	ENSP00000324375.5:p.Met607=
ENST00000264709.7:c.1821G=	ENSP00000264709.3:p.Met607=
ENST00000321117.9:c.1821G=	ENSP00000324375.5:p.Met607=
ENST00000380746.8:c.1254G=	ENSP00000370122.4:p.Met418=
ENST00000380756.7:c.1821G=	ENSP00000370132.3:p.Met607=
ENST00000402667.1:c.1152G=	ENSP00000384237.1:p.Met384=
ENST00000474887.5:n.140G=
NM_022552.4:c.1821G= , LRG_459t1:c.1821G=	NP_072046.2:p.Met607=
NM_153759.3:c.1254G= , LRG_459t2:c.1254G=	NP_715640.2:p.Met418=
NM_175629.2:c.1821G= , LRG_459t4:c.1821G=	NP_783328.1:p.Met607=
XM_005264175.3:c.1821G=	XP_005264232.1:p.Met607=
XM_005264177.3:c.1152G=	XP_005264234.1:p.Met384=
XM_006711957.2:c.1821G=	XP_006712020.1:p.Met607=
XM_006711958.2:c.1377G=	XP_006712021.1:p.Met459=
XM_011532662.1:c.1674G=	XP_011530964.1:p.Met558=
XM_011532663.1:c.1656G=	XP_011530965.1:p.Met552=
XM_011532664.1:c.1821G=	XP_011530966.1:p.Met607=
XM_011532665.1:c.1365G=	XP_011530967.1:p.Met455=
XM_011532666.1:c.1293G=	XP_011530968.1:p.Met431=
XM_011532667.1:c.1152G=	XP_011530969.1:p.Met384=
XM_011532668.1:c.1821G=	XP_011530970.1:p.Met607=
NM_001320893.1:c.1365G=	NP_001307822.1:p.Met455=
NR_135490.1:n.2159G=
XM_005264175.5:c.1821G=	XP_005264232.1:p.Met607=
XM_005264177.4:c.1152G=	XP_005264234.1:p.Met384=
XM_011532662.2:c.1674G=	XP_011530964.1:p.Met558=
XM_011532663.2:c.1656G=	XP_011530965.1:p.Met552=
XM_011532664.2:c.1821G=	XP_011530966.1:p.Met607=
XM_011532666.2:c.1293G=	XP_011530968.1:p.Met431=
XM_011532667.3:c.1152G=	XP_011530969.1:p.Met384=
XM_017003526.1:c.1821G=	XP_016859015.1:p.Met607=
XM_017003527.1:c.1152G=	XP_016859016.1:p.Met384=
XR_001738657.1:n.2098G=
NM_001375819.1:c.1152G=	NP_001362748.1:p.Met384=
NR_135490.2:n.2052G=
NM_022552.5:c.1821G= MANE Select	NP_072046.2:p.Met607=