Canonical Allele Identifier: CA346068197

Gene: DNMT3A

Linked Data

• COSMIC: COSM5424675 ; COSM5424676
• MyVariant Identifiers: chr2:g.25457251T>C (hg19) ; chr2:g.25234382T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234382T>C , CM000664.2:g.25234382T>C	GRCh38
NC_000002.11:g.25457251T>C , CM000664.1:g.25457251T>C	GRCh37
NC_000002.10:g.25310755T>C	NCBI36
NG_029465.2:g.113209A>G , LRG_459:g.113209A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.885A>G
ENST00000683393.1:c.1782A>G	ENSP00000508654.1:n.1782A>G
ENST00000683760.1:c.1967A>G	ENSP00000507765.1:p.Asn656Ser
ENST00000321117.10:c.2636A>G MANE Select	ENSP00000324375.5:p.Asn879Ser
ENST00000264709.7:c.2636A>G	ENSP00000264709.3:p.Asn879Ser
ENST00000321117.9:c.2636A>G	ENSP00000324375.5:p.Asn879Ser
ENST00000380746.8:c.2069A>G	ENSP00000370122.4:p.Asn690Ser
ENST00000380756.7:c.*489A>G	ENSP00000370132.3:n.*489A>G
ENST00000402667.1:c.1967A>G	ENSP00000384237.1:p.Asn656Ser
NM_022552.4:c.2636A>G , LRG_459t1:c.2636A>G	NP_072046.2:p.Asn879Ser
NM_153759.3:c.2069A>G , LRG_459t2:c.2069A>G	NP_715640.2:p.Asn690Ser
NM_175629.2:c.2636A>G , LRG_459t4:c.2636A>G	NP_783328.1:p.Asn879Ser
XM_005264175.3:c.2636A>G	XP_005264232.1:p.Asn879Ser
XM_005264177.3:c.1967A>G	XP_005264234.1:p.Asn656Ser
XM_006711958.2:c.2192A>G	XP_006712021.1:p.Asn731Ser
XM_011532662.1:c.2489A>G	XP_011530964.1:p.Asn830Ser
XM_011532663.1:c.2471A>G	XP_011530965.1:p.Asn824Ser
XM_011532665.1:c.2180A>G	XP_011530967.1:p.Asn727Ser
XM_011532666.1:c.2108A>G	XP_011530968.1:p.Asn703Ser
XM_011532667.1:c.1967A>G	XP_011530969.1:p.Asn656Ser
NM_001320893.1:c.2180A>G	NP_001307822.1:p.Asn727Ser
NR_135490.1:n.3173A>G
XM_005264175.5:c.2636A>G	XP_005264232.1:p.Asn879Ser
XM_005264177.4:c.1967A>G	XP_005264234.1:p.Asn656Ser
XM_011532662.2:c.2489A>G	XP_011530964.1:p.Asn830Ser
XM_011532663.2:c.2471A>G	XP_011530965.1:p.Asn824Ser
XM_011532666.2:c.2108A>G	XP_011530968.1:p.Asn703Ser
XM_011532667.3:c.1967A>G	XP_011530969.1:p.Asn656Ser
XM_017003526.1:c.2636A>G	XP_016859015.1:p.Asn879Ser
XM_017003527.1:c.1967A>G	XP_016859016.1:p.Asn656Ser
XR_001738657.1:n.2843A>G
NM_001375819.1:c.1967A>G	NP_001362748.1:p.Asn656Ser
NR_135490.2:n.3066A>G
NM_022552.5:c.2636A>G MANE Select	NP_072046.2:p.Asn879Ser