Canonical Allele Identifier: CA2576694339
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25244291_25244298del , CM000664.2:g.25244291_25244298del GRCh38
NC_000002.11:g.25467160_25467167del , CM000664.1:g.25467160_25467167del GRCh37
NC_000002.10:g.25320664_25320671del NCBI36
NG_029465.2:g.103293_103300del , LRG_459:g.103293_103300del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.27_34del
ENST00000683393.1:c.854_861del ENSP00000508654.1:n.854_861del
ENST00000683760.1:c.1039_1046del ENSP00000507765.1:p.Gly347ProfsTer5
ENST00000321117.10:c.1708_1715del MANE Select ENSP00000324375.5:p.Gly570ProfsTer5
ENST00000264709.7:c.1708_1715del ENSP00000264709.3:p.Gly570ProfsTer5
ENST00000321117.9:c.1708_1715del ENSP00000324375.5:p.Gly570ProfsTer5
ENST00000380746.8:c.1141_1148del ENSP00000370122.4:p.Gly381ProfsTer5
ENST00000380756.7:c.1708_1715del ENSP00000370132.3:p.Gly570ProfsTer5
ENST00000402667.1:c.1039_1046del ENSP00000384237.1:p.Gly347ProfsTer5
ENST00000474887.5:n.27_34del
NM_022552.4:c.1708_1715del , LRG_459t1:c.1708_1715del NP_072046.2:p.Gly570ProfsTer5
NM_153759.3:c.1141_1148del , LRG_459t2:c.1141_1148del NP_715640.2:p.Gly381ProfsTer5
NM_175629.2:c.1708_1715del , LRG_459t4:c.1708_1715del NP_783328.1:p.Gly570ProfsTer5
XM_005264175.3:c.1708_1715del XP_005264232.1:p.Gly570ProfsTer5
XM_005264177.3:c.1039_1046del XP_005264234.1:p.Gly347ProfsTer5
XM_006711957.2:c.1708_1715del XP_006712020.1:p.Gly570ProfsTer5
XM_006711958.2:c.1264_1271del XP_006712021.1:p.Gly422ProfsTer5
XM_011532662.1:c.1561_1568del XP_011530964.1:p.Gly521ProfsTer5
XM_011532663.1:c.1543_1550del XP_011530965.1:p.Gly515ProfsTer5
XM_011532664.1:c.1708_1715del XP_011530966.1:p.Gly570ProfsTer5
XM_011532665.1:c.1252_1259del XP_011530967.1:p.Gly418ProfsTer5
XM_011532666.1:c.1180_1187del XP_011530968.1:p.Gly394ProfsTer5
XM_011532667.1:c.1039_1046del XP_011530969.1:p.Gly347ProfsTer5
XM_011532668.1:c.1708_1715del XP_011530970.1:p.Gly570ProfsTer5
NM_001320893.1:c.1252_1259del NP_001307822.1:p.Gly418ProfsTer5
NR_135490.1:n.2046_2053del
XM_005264175.5:c.1708_1715del XP_005264232.1:p.Gly570ProfsTer5
XM_005264177.4:c.1039_1046del XP_005264234.1:p.Gly347ProfsTer5
XM_011532662.2:c.1561_1568del XP_011530964.1:p.Gly521ProfsTer5
XM_011532663.2:c.1543_1550del XP_011530965.1:p.Gly515ProfsTer5
XM_011532664.2:c.1708_1715del XP_011530966.1:p.Gly570ProfsTer5
XM_011532666.2:c.1180_1187del XP_011530968.1:p.Gly394ProfsTer5
XM_011532667.3:c.1039_1046del XP_011530969.1:p.Gly347ProfsTer5
XM_017003526.1:c.1708_1715del XP_016859015.1:p.Gly570ProfsTer5
XM_017003527.1:c.1039_1046del XP_016859016.1:p.Gly347ProfsTer5
XR_001738657.1:n.1985_1992del
NM_001375819.1:c.1039_1046del NP_001362748.1:p.Gly347ProfsTer5
NR_135490.2:n.1939_1946del
NM_022552.5:c.1708_1715del MANE Select NP_072046.2:p.Gly570ProfsTer5