Canonical Allele Identifier: CA425182155
Gene: DNMT3A HGNC NCBI

Linked Data

COSMIC: COSM144561
MyVariant Identifiers: chr2:g.25466851del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25243983del , CM000664.2:g.25243983del GRCh38
NC_000002.11:g.25466852del , CM000664.1:g.25466852del GRCh37
NC_000002.10:g.25320356del NCBI36
NG_029465.2:g.103609del , LRG_459:g.103609del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.171del
ENST00000683393.1:c.998del
ENST00000683760.1:c.1183del
ENST00000321117.10:c.1852del
ENST00000264709.7:c.1852del
ENST00000321117.9:c.1852del
ENST00000380746.8:c.1285del
ENST00000380756.7:c.1852del
ENST00000402667.1:c.1183del
ENST00000474887.5:n.171del
NM_022552.4:c.1852del , LRG_459t1:c.1852del
NM_153759.3:c.1285del , LRG_459t2:c.1285del
NM_175629.2:c.1852del , LRG_459t4:c.1852del
XM_005264175.3:c.1852del
XM_005264177.3:c.1183del
XM_006711957.2:c.1852del
XM_006711958.2:c.1408del
XM_011532662.1:c.1705del
XM_011532663.1:c.1687del
XM_011532664.1:c.1852del
XM_011532665.1:c.1396del
XM_011532666.1:c.1324del
XM_011532667.1:c.1183del
XM_011532668.1:c.1852del
NM_001320893.1:c.1396del
NR_135490.1:n.2190del
XM_005264175.5:c.1852del
XM_005264177.4:c.1183del
XM_011532662.2:c.1705del
XM_011532663.2:c.1687del
XM_011532664.2:c.1852del
XM_011532666.2:c.1324del
XM_011532667.3:c.1183del
XM_017003526.1:c.1852del
XM_017003527.1:c.1183del
XR_001738657.1:n.2129del
NM_001375819.1:c.1183del
NR_135490.2:n.2083del
NM_022552.5:c.1852del