Canonical Allele Identifier: CA1028525262
Gene: DNMT3A HGNC NCBI

Linked Data

dbSNP Id: rs1673046297

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25234064dup , CM000664.2:g.25234064dup GRCh38
NC_000002.11:g.25456933dup , CM000664.1:g.25456933dup GRCh37
NC_000002.10:g.25310437dup NCBI36
NG_029465.2:g.113528dup , LRG_459:g.113528dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000683393.1:c.2101dup ENSP00000508654.1:n.2101dup
ENST00000683760.1:c.*216dup ENSP00000507765.1:n.*216dup
ENST00000321117.10:c.*216dup MANE Select ENSP00000324375.5:n.*216dup
ENST00000264709.7:c.*216dup ENSP00000264709.3:n.*216dup
ENST00000321117.9:c.*216dup ENSP00000324375.5:n.*216dup
ENST00000380746.8:c.*216dup ENSP00000370122.4:n.*216dup
ENST00000380756.7:c.*808dup ENSP00000370132.3:n.*808dup
NM_022552.4:c.*216dup , LRG_459t1:c.*216dup NP_072046.2:n.*216dup
NM_153759.3:c.*216dup , LRG_459t2:c.*216dup NP_715640.2:n.*216dup
NM_175629.2:c.*216dup , LRG_459t4:c.*216dup NP_783328.1:n.*216dup
XM_005264175.3:c.*216dup XP_005264232.1:n.*216dup
XM_005264177.3:c.*216dup XP_005264234.1:n.*216dup
XM_006711958.2:c.*216dup XP_006712021.1:n.*216dup
XM_011532662.1:c.*216dup XP_011530964.1:n.*216dup
XM_011532663.1:c.*216dup XP_011530965.1:n.*216dup
XM_011532665.1:c.*216dup XP_011530967.1:n.*216dup
XM_011532666.1:c.*216dup XP_011530968.1:n.*216dup
XM_011532667.1:c.*216dup XP_011530969.1:n.*216dup
NM_001320893.1:c.*216dup NP_001307822.1:n.*216dup
NR_135490.1:n.3492dup
XM_005264175.5:c.*216dup XP_005264232.1:n.*216dup
XM_005264177.4:c.*216dup XP_005264234.1:n.*216dup
XM_011532662.2:c.*216dup XP_011530964.1:n.*216dup
XM_011532663.2:c.*216dup XP_011530965.1:n.*216dup
XM_011532666.2:c.*216dup XP_011530968.1:n.*216dup
XM_011532667.3:c.*216dup XP_011530969.1:n.*216dup
XM_017003526.1:c.*216dup XP_016859015.1:n.*216dup
XM_017003527.1:c.*216dup XP_016859016.1:n.*216dup
XR_001738657.1:n.3162dup
NM_001375819.1:c.*216dup NP_001362748.1:n.*216dup
NR_135490.2:n.3385dup
NM_022552.5:c.*216dup MANE Select NP_072046.2:n.*216dup