Canonical Allele Identifier: CA1239260264

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234312_25234314delinsGAA , CM000664.2:g.25234312_25234314delinsGAA	GRCh38
NC_000002.11:g.25457181_25457183delinsGAA , CM000664.1:g.25457181_25457183delinsGAA	GRCh37
NC_000002.10:g.25310685_25310687delinsGAA	NCBI36
NG_029465.2:g.113277_113279delinsTTC , LRG_459:g.113277_113279delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.953_955delinsTTC
ENST00000683393.1:c.1850_1852delinsTTC	ENSP00000508654.1:n.1850_1852delinsTTC
ENST00000683760.1:c.2035_2037delinsTTC	ENSP00000507765.1:p.Phe679=
ENST00000321117.10:c.2704_2706delinsTTC MANE Select	ENSP00000324375.5:p.Phe902=
ENST00000264709.7:c.2704_2706delinsTTC	ENSP00000264709.3:p.Phe902=
ENST00000321117.9:c.2704_2706delinsTTC	ENSP00000324375.5:p.Phe902=
ENST00000380746.8:c.2137_2139delinsTTC	ENSP00000370122.4:p.Phe713=
ENST00000380756.7:c.*557_*559delinsTTC	ENSP00000370132.3:n.*557_*559delinsTTC
ENST00000402667.1:c.2035_2037delinsTTC	ENSP00000384237.1:p.Phe679=
NM_022552.4:c.2704_2706delinsTTC , LRG_459t1:c.2704_2706delinsTTC	NP_072046.2:p.Phe902=
NM_153759.3:c.2137_2139delinsTTC , LRG_459t2:c.2137_2139delinsTTC	NP_715640.2:p.Phe713=
NM_175629.2:c.2704_2706delinsTTC , LRG_459t4:c.2704_2706delinsTTC	NP_783328.1:p.Phe902=
XM_005264175.3:c.2704_2706delinsTTC	XP_005264232.1:p.Phe902=
XM_005264177.3:c.2035_2037delinsTTC	XP_005264234.1:p.Phe679=
XM_006711958.2:c.2260_2262delinsTTC	XP_006712021.1:p.Phe754=
XM_011532662.1:c.2557_2559delinsTTC	XP_011530964.1:p.Phe853=
XM_011532663.1:c.2539_2541delinsTTC	XP_011530965.1:p.Phe847=
XM_011532665.1:c.2248_2250delinsTTC	XP_011530967.1:p.Phe750=
XM_011532666.1:c.2176_2178delinsTTC	XP_011530968.1:p.Phe726=
XM_011532667.1:c.2035_2037delinsTTC	XP_011530969.1:p.Phe679=
NM_001320893.1:c.2248_2250delinsTTC	NP_001307822.1:p.Phe750=
NR_135490.1:n.3241_3243delinsTTC
XM_005264175.5:c.2704_2706delinsTTC	XP_005264232.1:p.Phe902=
XM_005264177.4:c.2035_2037delinsTTC	XP_005264234.1:p.Phe679=
XM_011532662.2:c.2557_2559delinsTTC	XP_011530964.1:p.Phe853=
XM_011532663.2:c.2539_2541delinsTTC	XP_011530965.1:p.Phe847=
XM_011532666.2:c.2176_2178delinsTTC	XP_011530968.1:p.Phe726=
XM_011532667.3:c.2035_2037delinsTTC	XP_011530969.1:p.Phe679=
XM_017003526.1:c.2704_2706delinsTTC	XP_016859015.1:p.Phe902=
XM_017003527.1:c.2035_2037delinsTTC	XP_016859016.1:p.Phe679=
XR_001738657.1:n.2911_2913delinsTTC
NM_001375819.1:c.2035_2037delinsTTC	NP_001362748.1:p.Phe679=
NR_135490.2:n.3134_3136delinsTTC
NM_022552.5:c.2704_2706delinsTTC MANE Select	NP_072046.2:p.Phe902=