Canonical Allele Identifier: CA1239260279

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234327G= , CM000664.2:g.25234327G=	GRCh38
NC_000002.11:g.25457196G= , CM000664.1:g.25457196G=	GRCh37
NC_000002.10:g.25310700G=	NCBI36
NG_029465.2:g.113264C= , LRG_459:g.113264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.940C=
ENST00000683393.1:c.1837C=	ENSP00000508654.1:n.1837C=
ENST00000683760.1:c.2022C=	ENSP00000507765.1:p.Val674=
ENST00000321117.10:c.2691C= MANE Select	ENSP00000324375.5:p.Val897=
ENST00000264709.7:c.2691C=	ENSP00000264709.3:p.Val897=
ENST00000321117.9:c.2691C=	ENSP00000324375.5:p.Val897=
ENST00000380746.8:c.2124C=	ENSP00000370122.4:p.Val708=
ENST00000380756.7:c.*544C=	ENSP00000370132.3:n.*544C=
ENST00000402667.1:c.2022C=	ENSP00000384237.1:p.Val674=
NM_022552.4:c.2691C= , LRG_459t1:c.2691C=	NP_072046.2:p.Val897=
NM_153759.3:c.2124C= , LRG_459t2:c.2124C=	NP_715640.2:p.Val708=
NM_175629.2:c.2691C= , LRG_459t4:c.2691C=	NP_783328.1:p.Val897=
XM_005264175.3:c.2691C=	XP_005264232.1:p.Val897=
XM_005264177.3:c.2022C=	XP_005264234.1:p.Val674=
XM_006711958.2:c.2247C=	XP_006712021.1:p.Val749=
XM_011532662.1:c.2544C=	XP_011530964.1:p.Val848=
XM_011532663.1:c.2526C=	XP_011530965.1:p.Val842=
XM_011532665.1:c.2235C=	XP_011530967.1:p.Val745=
XM_011532666.1:c.2163C=	XP_011530968.1:p.Val721=
XM_011532667.1:c.2022C=	XP_011530969.1:p.Val674=
NM_001320893.1:c.2235C=	NP_001307822.1:p.Val745=
NR_135490.1:n.3228C=
XM_005264175.5:c.2691C=	XP_005264232.1:p.Val897=
XM_005264177.4:c.2022C=	XP_005264234.1:p.Val674=
XM_011532662.2:c.2544C=	XP_011530964.1:p.Val848=
XM_011532663.2:c.2526C=	XP_011530965.1:p.Val842=
XM_011532666.2:c.2163C=	XP_011530968.1:p.Val721=
XM_011532667.3:c.2022C=	XP_011530969.1:p.Val674=
XM_017003526.1:c.2691C=	XP_016859015.1:p.Val897=
XM_017003527.1:c.2022C=	XP_016859016.1:p.Val674=
XR_001738657.1:n.2898C=
NM_001375819.1:c.2022C=	NP_001362748.1:p.Val674=
NR_135490.2:n.3121C=
NM_022552.5:c.2691C= MANE Select	NP_072046.2:p.Val897=