Canonical Allele Identifier: CA1239254634
Gene: DNMT3A HGNC NCBI

Linked Data

dbSNP Id: rs1673105651

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234383_25234398del , CM000664.2:g.25234383_25234398del GRCh38
NC_000002.11:g.25457252_25457267del , CM000664.1:g.25457252_25457267del GRCh37
NC_000002.10:g.25310756_25310771del NCBI36
NG_029465.2:g.113193_113208del , LRG_459:g.113193_113208del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.869_884del
ENST00000683393.1:c.1766_1781del ENSP00000508654.1:n.1766_1781del
ENST00000683760.1:c.1951_1966del ENSP00000507765.1:p.Tyr651ThrfsTer2
ENST00000321117.10:c.2620_2635del MANE Select ENSP00000324375.5:p.Tyr874ThrfsTer2
ENST00000264709.7:c.2620_2635del ENSP00000264709.3:p.Tyr874ThrfsTer2
ENST00000321117.9:c.2620_2635del ENSP00000324375.5:p.Tyr874ThrfsTer2
ENST00000380746.8:c.2053_2068del ENSP00000370122.4:p.Tyr685ThrfsTer2
ENST00000380756.7:c.*473_*488del ENSP00000370132.3:n.*473_*488del
ENST00000402667.1:c.1951_1966del ENSP00000384237.1:p.Tyr651ThrfsTer2
NM_022552.4:c.2620_2635del , LRG_459t1:c.2620_2635del NP_072046.2:p.Tyr874ThrfsTer2
NM_153759.3:c.2053_2068del , LRG_459t2:c.2053_2068del NP_715640.2:p.Tyr685ThrfsTer2
NM_175629.2:c.2620_2635del , LRG_459t4:c.2620_2635del NP_783328.1:p.Tyr874ThrfsTer2
XM_005264175.3:c.2620_2635del XP_005264232.1:p.Tyr874ThrfsTer2
XM_005264177.3:c.1951_1966del XP_005264234.1:p.Tyr651ThrfsTer2
XM_006711958.2:c.2176_2191del XP_006712021.1:p.Tyr726ThrfsTer2
XM_011532662.1:c.2473_2488del XP_011530964.1:p.Tyr825ThrfsTer2
XM_011532663.1:c.2455_2470del XP_011530965.1:p.Tyr819ThrfsTer2
XM_011532665.1:c.2164_2179del XP_011530967.1:p.Tyr722ThrfsTer2
XM_011532666.1:c.2092_2107del XP_011530968.1:p.Tyr698ThrfsTer2
XM_011532667.1:c.1951_1966del XP_011530969.1:p.Tyr651ThrfsTer2
NM_001320893.1:c.2164_2179del NP_001307822.1:p.Tyr722ThrfsTer2
NR_135490.1:n.3157_3172del
XM_005264175.5:c.2620_2635del XP_005264232.1:p.Tyr874ThrfsTer2
XM_005264177.4:c.1951_1966del XP_005264234.1:p.Tyr651ThrfsTer2
XM_011532662.2:c.2473_2488del XP_011530964.1:p.Tyr825ThrfsTer2
XM_011532663.2:c.2455_2470del XP_011530965.1:p.Tyr819ThrfsTer2
XM_011532666.2:c.2092_2107del XP_011530968.1:p.Tyr698ThrfsTer2
XM_011532667.3:c.1951_1966del XP_011530969.1:p.Tyr651ThrfsTer2
XM_017003526.1:c.2620_2635del XP_016859015.1:p.Tyr874ThrfsTer2
XM_017003527.1:c.1951_1966del XP_016859016.1:p.Tyr651ThrfsTer2
XR_001738657.1:n.2827_2842del
NM_001375819.1:c.1951_1966del NP_001362748.1:p.Tyr651ThrfsTer2
NR_135490.2:n.3050_3065del
NM_022552.5:c.2620_2635del MANE Select NP_072046.2:p.Tyr874ThrfsTer2