Canonical Allele Identifier: CA346068056
Gene: DNMT3A HGNC NCBI

Linked Data

dbSNP Id: rs200800201

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234312G>C , CM000664.2:g.25234312G>C GRCh38
NC_000002.11:g.25457181G>C , CM000664.1:g.25457181G>C GRCh37
NC_000002.10:g.25310685G>C NCBI36
NG_029465.2:g.113279C>G , LRG_459:g.113279C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.955C>G
ENST00000683393.1:c.1852C>G ENSP00000508654.1:n.1852C>G
ENST00000683760.1:c.2037C>G ENSP00000507765.1:p.Phe679Leu
ENST00000321117.10:c.2706C>G MANE Select ENSP00000324375.5:p.Phe902Leu
ENST00000264709.7:c.2706C>G ENSP00000264709.3:p.Phe902Leu
ENST00000321117.9:c.2706C>G ENSP00000324375.5:p.Phe902Leu
ENST00000380746.8:c.2139C>G ENSP00000370122.4:p.Phe713Leu
ENST00000380756.7:c.*559C>G ENSP00000370132.3:n.*559C>G
ENST00000402667.1:c.2037C>G ENSP00000384237.1:p.Phe679Leu
NM_022552.4:c.2706C>G , LRG_459t1:c.2706C>G NP_072046.2:p.Phe902Leu
NM_153759.3:c.2139C>G , LRG_459t2:c.2139C>G NP_715640.2:p.Phe713Leu
NM_175629.2:c.2706C>G , LRG_459t4:c.2706C>G NP_783328.1:p.Phe902Leu
XM_005264175.3:c.2706C>G XP_005264232.1:p.Phe902Leu
XM_005264177.3:c.2037C>G XP_005264234.1:p.Phe679Leu
XM_006711958.2:c.2262C>G XP_006712021.1:p.Phe754Leu
XM_011532662.1:c.2559C>G XP_011530964.1:p.Phe853Leu
XM_011532663.1:c.2541C>G XP_011530965.1:p.Phe847Leu
XM_011532665.1:c.2250C>G XP_011530967.1:p.Phe750Leu
XM_011532666.1:c.2178C>G XP_011530968.1:p.Phe726Leu
XM_011532667.1:c.2037C>G XP_011530969.1:p.Phe679Leu
NM_001320893.1:c.2250C>G NP_001307822.1:p.Phe750Leu
NR_135490.1:n.3243C>G
XM_005264175.5:c.2706C>G XP_005264232.1:p.Phe902Leu
XM_005264177.4:c.2037C>G XP_005264234.1:p.Phe679Leu
XM_011532662.2:c.2559C>G XP_011530964.1:p.Phe853Leu
XM_011532663.2:c.2541C>G XP_011530965.1:p.Phe847Leu
XM_011532666.2:c.2178C>G XP_011530968.1:p.Phe726Leu
XM_011532667.3:c.2037C>G XP_011530969.1:p.Phe679Leu
XM_017003526.1:c.2706C>G XP_016859015.1:p.Phe902Leu
XM_017003527.1:c.2037C>G XP_016859016.1:p.Phe679Leu
XR_001738657.1:n.2913C>G
NM_001375819.1:c.2037C>G NP_001362748.1:p.Phe679Leu
NR_135490.2:n.3136C>G
NM_022552.5:c.2706C>G MANE Select NP_072046.2:p.Phe902Leu