Canonical Allele Identifier: CA1239265745

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25246626_25246639delinsGTGGCTCCAGGCCC , CM000664.2:g.25246626_25246639delinsGTGGCTCCAGGCCC	GRCh38
NC_000002.11:g.25469495_25469508delinsGTGGCTCCAGGCCC , CM000664.1:g.25469495_25469508delinsGTGGCTCCAGGCCC	GRCh37
NC_000002.10:g.25322999_25323012delinsGTGGCTCCAGGCCC	NCBI36
NG_029465.2:g.100952_100965delinsGGGCCTGGAGCCAC , LRG_459:g.100952_100965delinsGGGCCTGGAGCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.406_419delinsGGGCCTGGAGCCAC	ENSP00000508654.1:n.406_419delinsGGGCCTGGAGCCAC
ENST00000683760.1:c.591_604delinsGGGCCTGGAGCCAC	ENSP00000507765.1:p.Lys197=
ENST00000321117.10:c.1260_1273delinsGGGCCTGGAGCCAC MANE Select	ENSP00000324375.5:p.Lys420=
ENST00000264709.7:c.1260_1273delinsGGGCCTGGAGCCAC	ENSP00000264709.3:p.Lys420=
ENST00000321117.9:c.1260_1273delinsGGGCCTGGAGCCAC	ENSP00000324375.5:p.Lys420=
ENST00000380746.8:c.693_706delinsGGGCCTGGAGCCAC	ENSP00000370122.4:p.Lys231=
ENST00000380756.7:c.1260_1273delinsGGGCCTGGAGCCAC	ENSP00000370132.3:p.Lys420=
ENST00000402667.1:c.591_604delinsGGGCCTGGAGCCAC	ENSP00000384237.1:p.Lys197=
ENST00000474807.5:n.555_568delinsGGGCCTGGAGCCAC
NM_022552.4:c.1260_1273delinsGGGCCTGGAGCCAC , LRG_459t1:c.1260_1273delinsGGGCCTGGAGCCAC	NP_072046.2:p.Lys420=
NM_153759.3:c.693_706delinsGGGCCTGGAGCCAC , LRG_459t2:c.693_706delinsGGGCCTGGAGCCAC	NP_715640.2:p.Lys231=
NM_175629.2:c.1260_1273delinsGGGCCTGGAGCCAC , LRG_459t4:c.1260_1273delinsGGGCCTGGAGCCAC	NP_783328.1:p.Lys420=
XM_005264175.3:c.1260_1273delinsGGGCCTGGAGCCAC	XP_005264232.1:p.Lys420=
XM_005264177.3:c.591_604delinsGGGCCTGGAGCCAC	XP_005264234.1:p.Lys197=
XM_006711957.2:c.1260_1273delinsGGGCCTGGAGCCAC	XP_006712020.1:p.Lys420=
XM_006711958.2:c.816_829delinsGGGCCTGGAGCCAC	XP_006712021.1:p.Lys272=
XM_011532662.1:c.1113_1126delinsGGGCCTGGAGCCAC	XP_011530964.1:p.Lys371=
XM_011532663.1:c.1095_1108delinsGGGCCTGGAGCCAC	XP_011530965.1:p.Lys365=
XM_011532664.1:c.1260_1273delinsGGGCCTGGAGCCAC	XP_011530966.1:p.Lys420=
XM_011532665.1:c.804_817delinsGGGCCTGGAGCCAC	XP_011530967.1:p.Lys268=
XM_011532666.1:c.732_745delinsGGGCCTGGAGCCAC	XP_011530968.1:p.Lys244=
XM_011532667.1:c.591_604delinsGGGCCTGGAGCCAC	XP_011530969.1:p.Lys197=
XM_011532668.1:c.1260_1273delinsGGGCCTGGAGCCAC	XP_011530970.1:p.Lys420=
NM_001320893.1:c.804_817delinsGGGCCTGGAGCCAC	NP_001307822.1:p.Lys268=
NR_135490.1:n.1598_1611delinsGGGCCTGGAGCCAC
XM_005264175.5:c.1260_1273delinsGGGCCTGGAGCCAC	XP_005264232.1:p.Lys420=
XM_005264177.4:c.591_604delinsGGGCCTGGAGCCAC	XP_005264234.1:p.Lys197=
XM_011532662.2:c.1113_1126delinsGGGCCTGGAGCCAC	XP_011530964.1:p.Lys371=
XM_011532663.2:c.1095_1108delinsGGGCCTGGAGCCAC	XP_011530965.1:p.Lys365=
XM_011532664.2:c.1260_1273delinsGGGCCTGGAGCCAC	XP_011530966.1:p.Lys420=
XM_011532666.2:c.732_745delinsGGGCCTGGAGCCAC	XP_011530968.1:p.Lys244=
XM_011532667.3:c.591_604delinsGGGCCTGGAGCCAC	XP_011530969.1:p.Lys197=
XM_017003526.1:c.1260_1273delinsGGGCCTGGAGCCAC	XP_016859015.1:p.Lys420=
XM_017003527.1:c.591_604delinsGGGCCTGGAGCCAC	XP_016859016.1:p.Lys197=
XR_001738657.1:n.1537_1550delinsGGGCCTGGAGCCAC
NM_001375819.1:c.591_604delinsGGGCCTGGAGCCAC	NP_001362748.1:p.Lys197=
NR_135490.2:n.1491_1504delinsGGGCCTGGAGCCAC
NM_022552.5:c.1260_1273delinsGGGCCTGGAGCCAC MANE Select	NP_072046.2:p.Lys420=