Canonical Allele Identifier: CA1239262795

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244212_25244213delinsTC , CM000664.2:g.25244212_25244213delinsTC	GRCh38
NC_000002.11:g.25467081_25467082delinsTC , CM000664.1:g.25467081_25467082delinsTC	GRCh37
NC_000002.10:g.25320585_25320586delinsTC	NCBI36
NG_029465.2:g.103378_103379delinsGA , LRG_459:g.103378_103379delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.112_113delinsGA
ENST00000683393.1:c.939_940delinsGA	ENSP00000508654.1:n.939_940delinsGA
ENST00000683760.1:c.1124_1125delinsGA	ENSP00000507765.1:p.Arg375=
ENST00000321117.10:c.1793_1794delinsGA MANE Select	ENSP00000324375.5:p.Arg598=
ENST00000264709.7:c.1793_1794delinsGA	ENSP00000264709.3:p.Arg598=
ENST00000321117.9:c.1793_1794delinsGA	ENSP00000324375.5:p.Arg598=
ENST00000380746.8:c.1226_1227delinsGA	ENSP00000370122.4:p.Arg409=
ENST00000380756.7:c.1793_1794delinsGA	ENSP00000370132.3:p.Arg598=
ENST00000402667.1:c.1124_1125delinsGA	ENSP00000384237.1:p.Arg375=
ENST00000474887.5:n.112_113delinsGA
NM_022552.4:c.1793_1794delinsGA , LRG_459t1:c.1793_1794delinsGA	NP_072046.2:p.Arg598=
NM_153759.3:c.1226_1227delinsGA , LRG_459t2:c.1226_1227delinsGA	NP_715640.2:p.Arg409=
NM_175629.2:c.1793_1794delinsGA , LRG_459t4:c.1793_1794delinsGA	NP_783328.1:p.Arg598=
XM_005264175.3:c.1793_1794delinsGA	XP_005264232.1:p.Arg598=
XM_005264177.3:c.1124_1125delinsGA	XP_005264234.1:p.Arg375=
XM_006711957.2:c.1793_1794delinsGA	XP_006712020.1:p.Arg598=
XM_006711958.2:c.1349_1350delinsGA	XP_006712021.1:p.Arg450=
XM_011532662.1:c.1646_1647delinsGA	XP_011530964.1:p.Arg549=
XM_011532663.1:c.1628_1629delinsGA	XP_011530965.1:p.Arg543=
XM_011532664.1:c.1793_1794delinsGA	XP_011530966.1:p.Arg598=
XM_011532665.1:c.1337_1338delinsGA	XP_011530967.1:p.Arg446=
XM_011532666.1:c.1265_1266delinsGA	XP_011530968.1:p.Arg422=
XM_011532667.1:c.1124_1125delinsGA	XP_011530969.1:p.Arg375=
XM_011532668.1:c.1793_1794delinsGA	XP_011530970.1:p.Arg598=
NM_001320893.1:c.1337_1338delinsGA	NP_001307822.1:p.Arg446=
NR_135490.1:n.2131_2132delinsGA
XM_005264175.5:c.1793_1794delinsGA	XP_005264232.1:p.Arg598=
XM_005264177.4:c.1124_1125delinsGA	XP_005264234.1:p.Arg375=
XM_011532662.2:c.1646_1647delinsGA	XP_011530964.1:p.Arg549=
XM_011532663.2:c.1628_1629delinsGA	XP_011530965.1:p.Arg543=
XM_011532664.2:c.1793_1794delinsGA	XP_011530966.1:p.Arg598=
XM_011532666.2:c.1265_1266delinsGA	XP_011530968.1:p.Arg422=
XM_011532667.3:c.1124_1125delinsGA	XP_011530969.1:p.Arg375=
XM_017003526.1:c.1793_1794delinsGA	XP_016859015.1:p.Arg598=
XM_017003527.1:c.1124_1125delinsGA	XP_016859016.1:p.Arg375=
XR_001738657.1:n.2070_2071delinsGA
NM_001375819.1:c.1124_1125delinsGA	NP_001362748.1:p.Arg375=
NR_135490.2:n.2024_2025delinsGA
NM_022552.5:c.1793_1794delinsGA MANE Select	NP_072046.2:p.Arg598=