Canonical Allele Identifier: CA531368336
Gene: DNMT3A HGNC NCBI

Linked Data

dbSNP Id: rs1434083579

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234402_25234414del , CM000664.2:g.25234402_25234414del GRCh38
NC_000002.11:g.25457271_25457283del , CM000664.1:g.25457271_25457283del GRCh37
NC_000002.10:g.25310775_25310787del NCBI36
NG_029465.2:g.113177_113189del , LRG_459:g.113177_113189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.853_865del
ENST00000683393.1:c.1750_1762del ENSP00000508654.1:n.1750_1762del
ENST00000683760.1:c.1935_1947del ENSP00000507765.1:p.Gly646ThrfsTer8
ENST00000321117.10:c.2604_2616del MANE Select ENSP00000324375.5:p.Gly869ThrfsTer8
ENST00000264709.7:c.2604_2616del ENSP00000264709.3:p.Gly869ThrfsTer8
ENST00000321117.9:c.2604_2616del ENSP00000324375.5:p.Gly869ThrfsTer8
ENST00000380746.8:c.2037_2049del ENSP00000370122.4:p.Gly680ThrfsTer8
ENST00000380756.7:c.*457_*469del ENSP00000370132.3:n.*457_*469del
ENST00000402667.1:c.1935_1947del ENSP00000384237.1:p.Gly646ThrfsTer8
NM_022552.4:c.2604_2616del , LRG_459t1:c.2604_2616del NP_072046.2:p.Gly869ThrfsTer8
NM_153759.3:c.2037_2049del , LRG_459t2:c.2037_2049del NP_715640.2:p.Gly680ThrfsTer8
NM_175629.2:c.2604_2616del , LRG_459t4:c.2604_2616del NP_783328.1:p.Gly869ThrfsTer8
XM_005264175.3:c.2604_2616del XP_005264232.1:p.Gly869ThrfsTer8
XM_005264177.3:c.1935_1947del XP_005264234.1:p.Gly646ThrfsTer8
XM_006711958.2:c.2160_2172del XP_006712021.1:p.Gly721ThrfsTer8
XM_011532662.1:c.2457_2469del XP_011530964.1:p.Gly820ThrfsTer8
XM_011532663.1:c.2439_2451del XP_011530965.1:p.Gly814ThrfsTer8
XM_011532665.1:c.2148_2160del XP_011530967.1:p.Gly717ThrfsTer8
XM_011532666.1:c.2076_2088del XP_011530968.1:p.Gly693ThrfsTer8
XM_011532667.1:c.1935_1947del XP_011530969.1:p.Gly646ThrfsTer8
NM_001320893.1:c.2148_2160del NP_001307822.1:p.Gly717ThrfsTer8
NR_135490.1:n.3141_3153del
XM_005264175.5:c.2604_2616del XP_005264232.1:p.Gly869ThrfsTer8
XM_005264177.4:c.1935_1947del XP_005264234.1:p.Gly646ThrfsTer8
XM_011532662.2:c.2457_2469del XP_011530964.1:p.Gly820ThrfsTer8
XM_011532663.2:c.2439_2451del XP_011530965.1:p.Gly814ThrfsTer8
XM_011532666.2:c.2076_2088del XP_011530968.1:p.Gly693ThrfsTer8
XM_011532667.3:c.1935_1947del XP_011530969.1:p.Gly646ThrfsTer8
XM_017003526.1:c.2604_2616del XP_016859015.1:p.Gly869ThrfsTer8
XM_017003527.1:c.1935_1947del XP_016859016.1:p.Gly646ThrfsTer8
XR_001738657.1:n.2811_2823del
NM_001375819.1:c.1935_1947del NP_001362748.1:p.Gly646ThrfsTer8
NR_135490.2:n.3034_3046del
NM_022552.5:c.2604_2616del MANE Select NP_072046.2:p.Gly869ThrfsTer8