Canonical Allele Identifier: CA1239265106
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25240307_25240308delinsGA , CM000664.2:g.25240307_25240308delinsGA GRCh38
NC_000002.11:g.25463176_25463177delinsGA , CM000664.1:g.25463176_25463177delinsGA GRCh37
NC_000002.10:g.25316680_25316681delinsGA NCBI36
NG_029465.2:g.107283_107284delinsTC , LRG_459:g.107283_107284delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.635_636delinsTC
ENST00000683393.1:c.1462_1463delinsTC ENSP00000508654.1:n.1462_1463delinsTC
ENST00000683760.1:c.1647_1648delinsTC ENSP00000507765.1:p.Phe549=
ENST00000321117.10:c.2316_2317delinsTC MANE Select ENSP00000324375.5:p.Phe772=
ENST00000264709.7:c.2316_2317delinsTC ENSP00000264709.3:p.Phe772=
ENST00000321117.9:c.2316_2317delinsTC ENSP00000324375.5:p.Phe772=
ENST00000380746.8:c.1749_1750delinsTC ENSP00000370122.4:p.Phe583=
ENST00000380756.7:c.2316_2317delinsTC ENSP00000370132.3:p.Phe772=
ENST00000402667.1:c.1647_1648delinsTC ENSP00000384237.1:p.Phe549=
ENST00000461228.1:n.535_536delinsTC
ENST00000466601.5:n.688_689delinsTC
ENST00000474887.5:n.635_636delinsTC
ENST00000482935.5:n.316_317delinsTC
ENST00000491288.5:n.310+332_310+333delinsTC
NM_022552.4:c.2316_2317delinsTC , LRG_459t1:c.2316_2317delinsTC NP_072046.2:p.Phe772=
NM_153759.3:c.1749_1750delinsTC , LRG_459t2:c.1749_1750delinsTC NP_715640.2:p.Phe583=
NM_175629.2:c.2316_2317delinsTC , LRG_459t4:c.2316_2317delinsTC NP_783328.1:p.Phe772=
XM_005264175.3:c.2316_2317delinsTC XP_005264232.1:p.Phe772=
XM_005264177.3:c.1647_1648delinsTC XP_005264234.1:p.Phe549=
XM_006711957.2:c.2316_2317delinsTC XP_006712020.1:p.Phe772=
XM_006711958.2:c.1872_1873delinsTC XP_006712021.1:p.Phe624=
XM_011532662.1:c.2169_2170delinsTC XP_011530964.1:p.Phe723=
XM_011532663.1:c.2151_2152delinsTC XP_011530965.1:p.Phe717=
XM_011532664.1:c.2316_2317delinsTC XP_011530966.1:p.Phe772=
XM_011532665.1:c.1860_1861delinsTC XP_011530967.1:p.Phe620=
XM_011532666.1:c.1788_1789delinsTC XP_011530968.1:p.Phe596=
XM_011532667.1:c.1647_1648delinsTC XP_011530969.1:p.Phe549=
XM_011532668.1:c.2316_2317delinsTC XP_011530970.1:p.Phe772=
NM_001320893.1:c.1860_1861delinsTC NP_001307822.1:p.Phe620=
NR_135490.1:n.2654_2655delinsTC
XM_005264175.5:c.2316_2317delinsTC XP_005264232.1:p.Phe772=
XM_005264177.4:c.1647_1648delinsTC XP_005264234.1:p.Phe549=
XM_011532662.2:c.2169_2170delinsTC XP_011530964.1:p.Phe723=
XM_011532663.2:c.2151_2152delinsTC XP_011530965.1:p.Phe717=
XM_011532664.2:c.2316_2317delinsTC XP_011530966.1:p.Phe772=
XM_011532666.2:c.1788_1789delinsTC XP_011530968.1:p.Phe596=
XM_011532667.3:c.1647_1648delinsTC XP_011530969.1:p.Phe549=
XM_017003526.1:c.2316_2317delinsTC XP_016859015.1:p.Phe772=
XM_017003527.1:c.1647_1648delinsTC XP_016859016.1:p.Phe549=
XR_001738657.1:n.2593_2594delinsTC
NM_001375819.1:c.1647_1648delinsTC NP_001362748.1:p.Phe549=
NR_135490.2:n.2547_2548delinsTC
NM_022552.5:c.2316_2317delinsTC MANE Select NP_072046.2:p.Phe772=