Canonical Allele Identifier: CA646567115

Gene: DNMT3A

Linked Data

• COSMIC: COSN15655332

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234260_25234261insT , CM000664.2:g.25234260_25234261insT	GRCh38
NC_000002.11:g.25457129_25457130insT , CM000664.1:g.25457129_25457130insT	GRCh37
NC_000002.10:g.25310633_25310634insT	NCBI36
NG_029465.2:g.113330_113331insA , LRG_459:g.113330_113331insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.1903_1904insA	ENSP00000508654.1:n.1903_1904insA
ENST00000683760.1:c.*18_*19insA	ENSP00000507765.1:n.*18_*19insA
ENST00000321117.10:c.*18_*19insA MANE Select	ENSP00000324375.5:n.*18_*19insA
ENST00000264709.7:c.*18_*19insA	ENSP00000264709.3:n.*18_*19insA
ENST00000321117.9:c.*18_*19insA	ENSP00000324375.5:n.*18_*19insA
ENST00000380746.8:c.*18_*19insA	ENSP00000370122.4:n.*18_*19insA
ENST00000380756.7:c.*610_*611insA	ENSP00000370132.3:n.*610_*611insA
ENST00000402667.1:c.*18_*19insA	ENSP00000384237.1:n.*18_*19insA
NM_022552.4:c.*18_*19insA , LRG_459t1:c.*18_*19insA	NP_072046.2:n.*18_*19insA
NM_153759.3:c.*18_*19insA , LRG_459t2:c.*18_*19insA	NP_715640.2:n.*18_*19insA
NM_175629.2:c.*18_*19insA , LRG_459t4:c.*18_*19insA	NP_783328.1:n.*18_*19insA
XM_005264175.3:c.*18_*19insA	XP_005264232.1:n.*18_*19insA
XM_005264177.3:c.*18_*19insA	XP_005264234.1:n.*18_*19insA
XM_006711958.2:c.*18_*19insA	XP_006712021.1:n.*18_*19insA
XM_011532662.1:c.*18_*19insA	XP_011530964.1:n.*18_*19insA
XM_011532663.1:c.*18_*19insA	XP_011530965.1:n.*18_*19insA
XM_011532665.1:c.*18_*19insA	XP_011530967.1:n.*18_*19insA
XM_011532666.1:c.*18_*19insA	XP_011530968.1:n.*18_*19insA
XM_011532667.1:c.*18_*19insA	XP_011530969.1:n.*18_*19insA
NM_001320893.1:c.*18_*19insA	NP_001307822.1:n.*18_*19insA
NR_135490.1:n.3294_3295insA
XM_005264175.5:c.*18_*19insA	XP_005264232.1:n.*18_*19insA
XM_005264177.4:c.*18_*19insA	XP_005264234.1:n.*18_*19insA
XM_011532662.2:c.*18_*19insA	XP_011530964.1:n.*18_*19insA
XM_011532663.2:c.*18_*19insA	XP_011530965.1:n.*18_*19insA
XM_011532666.2:c.*18_*19insA	XP_011530968.1:n.*18_*19insA
XM_011532667.3:c.*18_*19insA	XP_011530969.1:n.*18_*19insA
XM_017003526.1:c.*18_*19insA	XP_016859015.1:n.*18_*19insA
XM_017003527.1:c.*18_*19insA	XP_016859016.1:n.*18_*19insA
XR_001738657.1:n.2964_2965insA
NM_001375819.1:c.*18_*19insA	NP_001362748.1:n.*18_*19insA
NR_135490.2:n.3187_3188insA
NM_022552.5:c.*18_*19insA MANE Select	NP_072046.2:n.*18_*19insA