Canonical Allele Identifier: CA645515162

Gene: DNMT3A

Linked Data

• COSMIC: COSM5944473

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240314_25240315insCG , CM000664.2:g.25240314_25240315insCG	GRCh38
NC_000002.11:g.25463183_25463184insCG , CM000664.1:g.25463183_25463184insCG	GRCh37
NC_000002.10:g.25316687_25316688insCG	NCBI36
NG_029465.2:g.107276_107277insCG , LRG_459:g.107276_107277insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.628_629insCG
ENST00000683393.1:c.1455_1456insCG	ENSP00000508654.1:n.1455_1456insCG
ENST00000683760.1:c.1640_1641insCG	ENSP00000507765.1:p.Arg548GlyfsTer9
ENST00000321117.10:c.2309_2310insCG MANE Select	ENSP00000324375.5:p.Arg771GlyfsTer9
ENST00000264709.7:c.2309_2310insCG	ENSP00000264709.3:p.Arg771GlyfsTer9
ENST00000321117.9:c.2309_2310insCG	ENSP00000324375.5:p.Arg771GlyfsTer9
ENST00000380746.8:c.1742_1743insCG	ENSP00000370122.4:p.Arg582GlyfsTer9
ENST00000380756.7:c.2309_2310insCG	ENSP00000370132.3:p.Arg771GlyfsTer?
ENST00000402667.1:c.1640_1641insCG	ENSP00000384237.1:p.Arg548GlyfsTer9
ENST00000461228.1:n.528_529insCG
ENST00000466601.5:n.681_682insCG
ENST00000474887.5:n.628_629insCG
ENST00000482935.5:n.309_310insCG
ENST00000491288.5:n.310+325_310+326insCG
NM_022552.4:c.2309_2310insCG , LRG_459t1:c.2309_2310insCG	NP_072046.2:p.Arg771GlyfsTer9
NM_153759.3:c.1742_1743insCG , LRG_459t2:c.1742_1743insCG	NP_715640.2:p.Arg582GlyfsTer9
NM_175629.2:c.2309_2310insCG , LRG_459t4:c.2309_2310insCG	NP_783328.1:p.Arg771GlyfsTer9
XM_005264175.3:c.2309_2310insCG	XP_005264232.1:p.Arg771GlyfsTer9
XM_005264177.3:c.1640_1641insCG	XP_005264234.1:p.Arg548GlyfsTer9
XM_006711957.2:c.2309_2310insCG	XP_006712020.1:p.Arg771GlyfsTer9
XM_006711958.2:c.1865_1866insCG	XP_006712021.1:p.Arg623GlyfsTer9
XM_011532662.1:c.2162_2163insCG	XP_011530964.1:p.Arg722GlyfsTer9
XM_011532663.1:c.2144_2145insCG	XP_011530965.1:p.Arg716GlyfsTer9
XM_011532664.1:c.2309_2310insCG	XP_011530966.1:p.Arg771GlyfsTer?
XM_011532665.1:c.1853_1854insCG	XP_011530967.1:p.Arg619GlyfsTer9
XM_011532666.1:c.1781_1782insCG	XP_011530968.1:p.Arg595GlyfsTer9
XM_011532667.1:c.1640_1641insCG	XP_011530969.1:p.Arg548GlyfsTer9
XM_011532668.1:c.2309_2310insCG	XP_011530970.1:p.Arg771GlyfsTer?
NM_001320893.1:c.1853_1854insCG	NP_001307822.1:p.Arg619GlyfsTer9
NR_135490.1:n.2647_2648insCG
XM_005264175.5:c.2309_2310insCG	XP_005264232.1:p.Arg771GlyfsTer9
XM_005264177.4:c.1640_1641insCG	XP_005264234.1:p.Arg548GlyfsTer9
XM_011532662.2:c.2162_2163insCG	XP_011530964.1:p.Arg722GlyfsTer9
XM_011532663.2:c.2144_2145insCG	XP_011530965.1:p.Arg716GlyfsTer9
XM_011532664.2:c.2309_2310insCG	XP_011530966.1:p.Arg771GlyfsTer?
XM_011532666.2:c.1781_1782insCG	XP_011530968.1:p.Arg595GlyfsTer9
XM_011532667.3:c.1640_1641insCG	XP_011530969.1:p.Arg548GlyfsTer9
XM_017003526.1:c.2309_2310insCG	XP_016859015.1:p.Arg771GlyfsTer9
XM_017003527.1:c.1640_1641insCG	XP_016859016.1:p.Arg548GlyfsTer9
XR_001738657.1:n.2586_2587insCG
NM_001375819.1:c.1640_1641insCG	NP_001362748.1:p.Arg548GlyfsTer9
NR_135490.2:n.2540_2541insCG
NM_022552.5:c.2309_2310insCG MANE Select	NP_072046.2:p.Arg771GlyfsTer9