Canonical Allele Identifier: CA2838216060

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240324dup , CM000664.2:g.25240324dup	GRCh38
NC_000002.11:g.25463193dup , CM000664.1:g.25463193dup	GRCh37
NC_000002.10:g.25316697dup	NCBI36
NG_029465.2:g.107269dup , LRG_459:g.107269dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.621dup
ENST00000683393.1:c.1448dup	ENSP00000508654.1:n.1448dup
ENST00000683760.1:c.1633dup	ENSP00000507765.1:p.Asp545GlyfsTer14
ENST00000321117.10:c.2302dup MANE Select	ENSP00000324375.5:p.Asp768GlyfsTer14
ENST00000264709.7:c.2302dup	ENSP00000264709.3:p.Asp768GlyfsTer14
ENST00000321117.9:c.2302dup	ENSP00000324375.5:p.Asp768GlyfsTer14
ENST00000380746.8:c.1735dup	ENSP00000370122.4:p.Asp579GlyfsTer14
ENST00000380756.7:c.2302dup	ENSP00000370132.3:p.Asp768GlyfsTer11
ENST00000402667.1:c.1633dup	ENSP00000384237.1:p.Asp545GlyfsTer14
ENST00000461228.1:n.521dup
ENST00000466601.5:n.674dup
ENST00000474887.5:n.621dup
ENST00000482935.5:n.302dup
ENST00000491288.5:n.310+318dup
NM_022552.4:c.2302dup , LRG_459t1:c.2302dup	NP_072046.2:p.Asp768GlyfsTer14
NM_153759.3:c.1735dup , LRG_459t2:c.1735dup	NP_715640.2:p.Asp579GlyfsTer14
NM_175629.2:c.2302dup , LRG_459t4:c.2302dup	NP_783328.1:p.Asp768GlyfsTer14
XM_005264175.3:c.2302dup	XP_005264232.1:p.Asp768GlyfsTer14
XM_005264177.3:c.1633dup	XP_005264234.1:p.Asp545GlyfsTer14
XM_006711957.2:c.2302dup	XP_006712020.1:p.Asp768GlyfsTer14
XM_006711958.2:c.1858dup	XP_006712021.1:p.Asp620GlyfsTer14
XM_011532662.1:c.2155dup	XP_011530964.1:p.Asp719GlyfsTer14
XM_011532663.1:c.2137dup	XP_011530965.1:p.Asp713GlyfsTer14
XM_011532664.1:c.2302dup	XP_011530966.1:p.Asp768GlyfsTer11
XM_011532665.1:c.1846dup	XP_011530967.1:p.Asp616GlyfsTer14
XM_011532666.1:c.1774dup	XP_011530968.1:p.Asp592GlyfsTer14
XM_011532667.1:c.1633dup	XP_011530969.1:p.Asp545GlyfsTer14
XM_011532668.1:c.2302dup	XP_011530970.1:p.Asp768GlyfsTer11
NM_001320893.1:c.1846dup	NP_001307822.1:p.Asp616GlyfsTer14
NR_135490.1:n.2640dup
XM_005264175.5:c.2302dup	XP_005264232.1:p.Asp768GlyfsTer14
XM_005264177.4:c.1633dup	XP_005264234.1:p.Asp545GlyfsTer14
XM_011532662.2:c.2155dup	XP_011530964.1:p.Asp719GlyfsTer14
XM_011532663.2:c.2137dup	XP_011530965.1:p.Asp713GlyfsTer14
XM_011532664.2:c.2302dup	XP_011530966.1:p.Asp768GlyfsTer11
XM_011532666.2:c.1774dup	XP_011530968.1:p.Asp592GlyfsTer14
XM_011532667.3:c.1633dup	XP_011530969.1:p.Asp545GlyfsTer14
XM_017003526.1:c.2302dup	XP_016859015.1:p.Asp768GlyfsTer14
XM_017003527.1:c.1633dup	XP_016859016.1:p.Asp545GlyfsTer14
XR_001738657.1:n.2579dup
NM_001375819.1:c.1633dup	NP_001362748.1:p.Asp545GlyfsTer14
NR_135490.2:n.2533dup
NM_022552.5:c.2302dup MANE Select	NP_072046.2:p.Asp768GlyfsTer14