Canonical Allele Identifier: CA2576693911

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240368_25240369insC , CM000664.2:g.25240368_25240369insC	GRCh38
NC_000002.11:g.25463237_25463238insC , CM000664.1:g.25463237_25463238insC	GRCh37
NC_000002.10:g.25316741_25316742insC	NCBI36
NG_029465.2:g.107222_107223insG , LRG_459:g.107222_107223insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.574_575insG
ENST00000683393.1:c.1401_1402insG	ENSP00000508654.1:n.1401_1402insG
ENST00000683760.1:c.1586_1587insG	ENSP00000507765.1:p.Phe529LeufsTer5
ENST00000321117.10:c.2255_2256insG MANE Select	ENSP00000324375.5:p.Phe752LeufsTer5
ENST00000264709.7:c.2255_2256insG	ENSP00000264709.3:p.Phe752LeufsTer5
ENST00000321117.9:c.2255_2256insG	ENSP00000324375.5:p.Phe752LeufsTer5
ENST00000380746.8:c.1688_1689insG	ENSP00000370122.4:p.Phe563LeufsTer5
ENST00000380756.7:c.2255_2256insG	ENSP00000370132.3:p.Phe752LeufsTer5
ENST00000402667.1:c.1586_1587insG	ENSP00000384237.1:p.Phe529LeufsTer5
ENST00000461228.1:n.474_475insG
ENST00000466601.5:n.627_628insG
ENST00000474887.5:n.574_575insG
ENST00000482935.5:n.255_256insG
ENST00000491288.5:n.310+271_310+272insG
NM_022552.4:c.2255_2256insG , LRG_459t1:c.2255_2256insG	NP_072046.2:p.Phe752LeufsTer5
NM_153759.3:c.1688_1689insG , LRG_459t2:c.1688_1689insG	NP_715640.2:p.Phe563LeufsTer5
NM_175629.2:c.2255_2256insG , LRG_459t4:c.2255_2256insG	NP_783328.1:p.Phe752LeufsTer5
XM_005264175.3:c.2255_2256insG	XP_005264232.1:p.Phe752LeufsTer5
XM_005264177.3:c.1586_1587insG	XP_005264234.1:p.Phe529LeufsTer5
XM_006711957.2:c.2255_2256insG	XP_006712020.1:p.Phe752LeufsTer5
XM_006711958.2:c.1811_1812insG	XP_006712021.1:p.Phe604LeufsTer5
XM_011532662.1:c.2108_2109insG	XP_011530964.1:p.Phe703LeufsTer5
XM_011532663.1:c.2090_2091insG	XP_011530965.1:p.Phe697LeufsTer5
XM_011532664.1:c.2255_2256insG	XP_011530966.1:p.Phe752LeufsTer5
XM_011532665.1:c.1799_1800insG	XP_011530967.1:p.Phe600LeufsTer5
XM_011532666.1:c.1727_1728insG	XP_011530968.1:p.Phe576LeufsTer5
XM_011532667.1:c.1586_1587insG	XP_011530969.1:p.Phe529LeufsTer5
XM_011532668.1:c.2255_2256insG	XP_011530970.1:p.Phe752LeufsTer5
NM_001320893.1:c.1799_1800insG	NP_001307822.1:p.Phe600LeufsTer5
NR_135490.1:n.2593_2594insG
XM_005264175.5:c.2255_2256insG	XP_005264232.1:p.Phe752LeufsTer5
XM_005264177.4:c.1586_1587insG	XP_005264234.1:p.Phe529LeufsTer5
XM_011532662.2:c.2108_2109insG	XP_011530964.1:p.Phe703LeufsTer5
XM_011532663.2:c.2090_2091insG	XP_011530965.1:p.Phe697LeufsTer5
XM_011532664.2:c.2255_2256insG	XP_011530966.1:p.Phe752LeufsTer5
XM_011532666.2:c.1727_1728insG	XP_011530968.1:p.Phe576LeufsTer5
XM_011532667.3:c.1586_1587insG	XP_011530969.1:p.Phe529LeufsTer5
XM_017003526.1:c.2255_2256insG	XP_016859015.1:p.Phe752LeufsTer5
XM_017003527.1:c.1586_1587insG	XP_016859016.1:p.Phe529LeufsTer5
XR_001738657.1:n.2532_2533insG
NM_001375819.1:c.1586_1587insG	NP_001362748.1:p.Phe529LeufsTer5
NR_135490.2:n.2486_2487insG
NM_022552.5:c.2255_2256insG MANE Select	NP_072046.2:p.Phe752LeufsTer5