Canonical Allele Identifier: CA1239254526

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234356_25234358delinsGTC , CM000664.2:g.25234356_25234358delinsGTC	GRCh38
NC_000002.11:g.25457225_25457227delinsGTC , CM000664.1:g.25457225_25457227delinsGTC	GRCh37
NC_000002.10:g.25310729_25310731delinsGTC	NCBI36
NG_029465.2:g.113233_113235delinsGAC , LRG_459:g.113233_113235delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.909_911delinsGAC
ENST00000683393.1:c.1806_1808delinsGAC	ENSP00000508654.1:n.1806_1808delinsGAC
ENST00000683760.1:c.1991_1993delinsGAC	ENSP00000507765.1:p.Arg664=
ENST00000321117.10:c.2660_2662delinsGAC MANE Select	ENSP00000324375.5:p.Arg887=
ENST00000264709.7:c.2660_2662delinsGAC	ENSP00000264709.3:p.Arg887=
ENST00000321117.9:c.2660_2662delinsGAC	ENSP00000324375.5:p.Arg887=
ENST00000380746.8:c.2093_2095delinsGAC	ENSP00000370122.4:p.Arg698=
ENST00000380756.7:c.*513_*515delinsGAC	ENSP00000370132.3:n.*513_*515delinsGAC
ENST00000402667.1:c.1991_1993delinsGAC	ENSP00000384237.1:p.Arg664=
NM_022552.4:c.2660_2662delinsGAC , LRG_459t1:c.2660_2662delinsGAC	NP_072046.2:p.Arg887=
NM_153759.3:c.2093_2095delinsGAC , LRG_459t2:c.2093_2095delinsGAC	NP_715640.2:p.Arg698=
NM_175629.2:c.2660_2662delinsGAC , LRG_459t4:c.2660_2662delinsGAC	NP_783328.1:p.Arg887=
XM_005264175.3:c.2660_2662delinsGAC	XP_005264232.1:p.Arg887=
XM_005264177.3:c.1991_1993delinsGAC	XP_005264234.1:p.Arg664=
XM_006711958.2:c.2216_2218delinsGAC	XP_006712021.1:p.Arg739=
XM_011532662.1:c.2513_2515delinsGAC	XP_011530964.1:p.Arg838=
XM_011532663.1:c.2495_2497delinsGAC	XP_011530965.1:p.Arg832=
XM_011532665.1:c.2204_2206delinsGAC	XP_011530967.1:p.Arg735=
XM_011532666.1:c.2132_2134delinsGAC	XP_011530968.1:p.Arg711=
XM_011532667.1:c.1991_1993delinsGAC	XP_011530969.1:p.Arg664=
NM_001320893.1:c.2204_2206delinsGAC	NP_001307822.1:p.Arg735=
NR_135490.1:n.3197_3199delinsGAC
XM_005264175.5:c.2660_2662delinsGAC	XP_005264232.1:p.Arg887=
XM_005264177.4:c.1991_1993delinsGAC	XP_005264234.1:p.Arg664=
XM_011532662.2:c.2513_2515delinsGAC	XP_011530964.1:p.Arg838=
XM_011532663.2:c.2495_2497delinsGAC	XP_011530965.1:p.Arg832=
XM_011532666.2:c.2132_2134delinsGAC	XP_011530968.1:p.Arg711=
XM_011532667.3:c.1991_1993delinsGAC	XP_011530969.1:p.Arg664=
XM_017003526.1:c.2660_2662delinsGAC	XP_016859015.1:p.Arg887=
XM_017003527.1:c.1991_1993delinsGAC	XP_016859016.1:p.Arg664=
XR_001738657.1:n.2867_2869delinsGAC
NM_001375819.1:c.1991_1993delinsGAC	NP_001362748.1:p.Arg664=
NR_135490.2:n.3090_3092delinsGAC
NM_022552.5:c.2660_2662delinsGAC MANE Select	NP_072046.2:p.Arg887=