Canonical Allele Identifier: CA2699053721

Gene: DNMT3A

Linked Data

• dbSNP Id: rs2149270915

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240302del , CM000664.2:g.25240302del	GRCh38
NC_000002.11:g.25463171del , CM000664.1:g.25463171del	GRCh37
NC_000002.10:g.25316675del	NCBI36
NG_029465.2:g.107290del , LRG_459:g.107290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.641+1del
ENST00000683393.1:c.1468+1del
ENST00000683760.1:c.1653+1del
ENST00000321117.10:c.2322+1del
ENST00000264709.7:c.2322+1del
ENST00000321117.9:c.2322+1del
ENST00000380746.8:c.1755+1del
ENST00000380756.7:c.2322+1del
ENST00000402667.1:c.1653+1del
ENST00000461228.1:n.541+1del
ENST00000466601.5:n.694+1del
ENST00000474887.5:n.641+1del
ENST00000482935.5:n.322+1del
ENST00000491288.5:n.310+339del
NM_022552.4:c.2322+1del , LRG_459t1:c.2322+1del
NM_153759.3:c.1755+1del , LRG_459t2:c.1755+1del
NM_175629.2:c.2322+1del , LRG_459t4:c.2322+1del
XM_005264175.3:c.2322+1del
XM_005264177.3:c.1653+1del
XM_006711957.2:c.2322+1del
XM_006711958.2:c.1878+1del
XM_011532662.1:c.2175+1del
XM_011532663.1:c.2157+1del
XM_011532664.1:c.2322+1del
XM_011532665.1:c.1866+1del
XM_011532666.1:c.1794+1del
XM_011532667.1:c.1653+1del
XM_011532668.1:c.2322+1del
NM_001320893.1:c.1866+1del
NR_135490.1:n.2660+1del
XM_005264175.5:c.2322+1del
XM_005264177.4:c.1653+1del
XM_011532662.2:c.2175+1del
XM_011532663.2:c.2157+1del
XM_011532664.2:c.2322+1del
XM_011532666.2:c.1794+1del
XM_011532667.3:c.1653+1del
XM_017003526.1:c.2322+1del
XM_017003527.1:c.1653+1del
XR_001738657.1:n.2599+1del
NM_001375819.1:c.1653+1del
NR_135490.2:n.2553+1del
NM_022552.5:c.2322+1del