Canonical Allele Identifier: CA346073004
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25246640T>G , CM000664.2:g.25246640T>G GRCh38
NC_000002.11:g.25469509T>G , CM000664.1:g.25469509T>G GRCh37
NC_000002.10:g.25323013T>G NCBI36
NG_029465.2:g.100951A>C , LRG_459:g.100951A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683393.1:c.405A>C ENSP00000508654.1:n.405A>C
ENST00000683760.1:c.590A>C ENSP00000507765.1:p.Lys197Thr
ENST00000321117.10:c.1259A>C MANE Select ENSP00000324375.5:p.Lys420Thr
ENST00000264709.7:c.1259A>C ENSP00000264709.3:p.Lys420Thr
ENST00000321117.9:c.1259A>C ENSP00000324375.5:p.Lys420Thr
ENST00000380746.8:c.692A>C ENSP00000370122.4:p.Lys231Thr
ENST00000380756.7:c.1259A>C ENSP00000370132.3:p.Lys420Thr
ENST00000402667.1:c.590A>C ENSP00000384237.1:p.Lys197Thr
ENST00000474807.5:n.554A>C
NM_022552.4:c.1259A>C , LRG_459t1:c.1259A>C NP_072046.2:p.Lys420Thr
NM_153759.3:c.692A>C , LRG_459t2:c.692A>C NP_715640.2:p.Lys231Thr
NM_175629.2:c.1259A>C , LRG_459t4:c.1259A>C NP_783328.1:p.Lys420Thr
XM_005264175.3:c.1259A>C XP_005264232.1:p.Lys420Thr
XM_005264177.3:c.590A>C XP_005264234.1:p.Lys197Thr
XM_006711957.2:c.1259A>C XP_006712020.1:p.Lys420Thr
XM_006711958.2:c.815A>C XP_006712021.1:p.Lys272Thr
XM_011532662.1:c.1112A>C XP_011530964.1:p.Lys371Thr
XM_011532663.1:c.1094A>C XP_011530965.1:p.Lys365Thr
XM_011532664.1:c.1259A>C XP_011530966.1:p.Lys420Thr
XM_011532665.1:c.803A>C XP_011530967.1:p.Lys268Thr
XM_011532666.1:c.731A>C XP_011530968.1:p.Lys244Thr
XM_011532667.1:c.590A>C XP_011530969.1:p.Lys197Thr
XM_011532668.1:c.1259A>C XP_011530970.1:p.Lys420Thr
NM_001320893.1:c.803A>C NP_001307822.1:p.Lys268Thr
NR_135490.1:n.1597A>C
XM_005264175.5:c.1259A>C XP_005264232.1:p.Lys420Thr
XM_005264177.4:c.590A>C XP_005264234.1:p.Lys197Thr
XM_011532662.2:c.1112A>C XP_011530964.1:p.Lys371Thr
XM_011532663.2:c.1094A>C XP_011530965.1:p.Lys365Thr
XM_011532664.2:c.1259A>C XP_011530966.1:p.Lys420Thr
XM_011532666.2:c.731A>C XP_011530968.1:p.Lys244Thr
XM_011532667.3:c.590A>C XP_011530969.1:p.Lys197Thr
XM_017003526.1:c.1259A>C XP_016859015.1:p.Lys420Thr
XM_017003527.1:c.590A>C XP_016859016.1:p.Lys197Thr
XR_001738657.1:n.1536A>C
NM_001375819.1:c.590A>C NP_001362748.1:p.Lys197Thr
NR_135490.2:n.1490A>C
NM_022552.5:c.1259A>C MANE Select NP_072046.2:p.Lys420Thr