Canonical Allele Identifier: CA1239265759

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25246636_25246661delinsGCCCTTAGGGCCAGAAGGCTGGAAGC , CM000664.2:g.25246636_25246661delinsGCCCTTAGGGCCAGAAGGCTGGAAGC	GRCh38
NC_000002.11:g.25469505_25469530delinsGCCCTTAGGGCCAGAAGGCTGGAAGC , CM000664.1:g.25469505_25469530delinsGCCCTTAGGGCCAGAAGGCTGGAAGC	GRCh37
NC_000002.10:g.25323009_25323034delinsGCCCTTAGGGCCAGAAGGCTGGAAGC	NCBI36
NG_029465.2:g.100930_100955delinsGCTTCCAGCCTTCTGGCCCTAAGGGC , LRG_459:g.100930_100955delinsGCTTCCAGCCTTCTGGCCCTAAGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.384_409delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000508654.1:n.384_409delinsGCTTCCAGCCTTCTGGCCCTAAGGGC
ENST00000683760.1:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000507765.1:p.Gly190=
ENST00000321117.10:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC MANE Select	ENSP00000324375.5:p.Gly413=
ENST00000264709.7:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000264709.3:p.Gly413=
ENST00000321117.9:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000324375.5:p.Gly413=
ENST00000380746.8:c.671_696delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000370122.4:p.Gly224=
ENST00000380756.7:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000370132.3:p.Gly413=
ENST00000402667.1:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	ENSP00000384237.1:p.Gly190=
ENST00000474807.5:n.533_558delinsGCTTCCAGCCTTCTGGCCCTAAGGGC
NM_022552.4:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC , LRG_459t1:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	NP_072046.2:p.Gly413=
NM_153759.3:c.671_696delinsGCTTCCAGCCTTCTGGCCCTAAGGGC , LRG_459t2:c.671_696delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	NP_715640.2:p.Gly224=
NM_175629.2:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC , LRG_459t4:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	NP_783328.1:p.Gly413=
XM_005264175.3:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_005264232.1:p.Gly413=
XM_005264177.3:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_005264234.1:p.Gly190=
XM_006711957.2:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_006712020.1:p.Gly413=
XM_006711958.2:c.794_819delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_006712021.1:p.Gly265=
XM_011532662.1:c.1091_1116delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530964.1:p.Gly364=
XM_011532663.1:c.1073_1098delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530965.1:p.Gly358=
XM_011532664.1:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530966.1:p.Gly413=
XM_011532665.1:c.782_807delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530967.1:p.Gly261=
XM_011532666.1:c.710_735delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530968.1:p.Gly237=
XM_011532667.1:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530969.1:p.Gly190=
XM_011532668.1:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530970.1:p.Gly413=
NM_001320893.1:c.782_807delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	NP_001307822.1:p.Gly261=
NR_135490.1:n.1576_1601delinsGCTTCCAGCCTTCTGGCCCTAAGGGC
XM_005264175.5:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_005264232.1:p.Gly413=
XM_005264177.4:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_005264234.1:p.Gly190=
XM_011532662.2:c.1091_1116delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530964.1:p.Gly364=
XM_011532663.2:c.1073_1098delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530965.1:p.Gly358=
XM_011532664.2:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530966.1:p.Gly413=
XM_011532666.2:c.710_735delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530968.1:p.Gly237=
XM_011532667.3:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_011530969.1:p.Gly190=
XM_017003526.1:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_016859015.1:p.Gly413=
XM_017003527.1:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	XP_016859016.1:p.Gly190=
XR_001738657.1:n.1515_1540delinsGCTTCCAGCCTTCTGGCCCTAAGGGC
NM_001375819.1:c.569_594delinsGCTTCCAGCCTTCTGGCCCTAAGGGC	NP_001362748.1:p.Gly190=
NR_135490.2:n.1469_1494delinsGCTTCCAGCCTTCTGGCCCTAAGGGC
NM_022552.5:c.1238_1263delinsGCTTCCAGCCTTCTGGCCCTAAGGGC MANE Select	NP_072046.2:p.Gly413=