Canonical Allele Identifier: CA645515169

Gene: DNMT3A

Linked Data

• COSMIC: COSM1583111 ; COSM5944210

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240350_25240352del , CM000664.2:g.25240350_25240352del	GRCh38
NC_000002.11:g.25463219_25463221del , CM000664.1:g.25463219_25463221del	GRCh37
NC_000002.10:g.25316723_25316725del	NCBI36
NG_029465.2:g.107243_107245del , LRG_459:g.107243_107245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.595_597del
ENST00000683393.1:c.1422_1424del	ENSP00000508654.1:n.1422_1424del
ENST00000683760.1:c.1607_1609del	ENSP00000507765.1:p.Val536del
ENST00000321117.10:c.2276_2278del MANE Select	ENSP00000324375.5:p.Val759del
ENST00000264709.7:c.2276_2278del	ENSP00000264709.3:p.Val759del
ENST00000321117.9:c.2276_2278del	ENSP00000324375.5:p.Val759del
ENST00000380746.8:c.1709_1711del	ENSP00000370122.4:p.Val570del
ENST00000380756.7:c.2276_2278del	ENSP00000370132.3:p.Val759del
ENST00000402667.1:c.1607_1609del	ENSP00000384237.1:p.Val536del
ENST00000461228.1:n.495_497del
ENST00000466601.5:n.648_650del
ENST00000474887.5:n.595_597del
ENST00000482935.5:n.276_278del
ENST00000491288.5:n.310+292_310+294del
NM_022552.4:c.2276_2278del , LRG_459t1:c.2276_2278del	NP_072046.2:p.Val759del
NM_153759.3:c.1709_1711del , LRG_459t2:c.1709_1711del	NP_715640.2:p.Val570del
NM_175629.2:c.2276_2278del , LRG_459t4:c.2276_2278del	NP_783328.1:p.Val759del
XM_005264175.3:c.2276_2278del	XP_005264232.1:p.Val759del
XM_005264177.3:c.1607_1609del	XP_005264234.1:p.Val536del
XM_006711957.2:c.2276_2278del	XP_006712020.1:p.Val759del
XM_006711958.2:c.1832_1834del	XP_006712021.1:p.Val611del
XM_011532662.1:c.2129_2131del	XP_011530964.1:p.Val710del
XM_011532663.1:c.2111_2113del	XP_011530965.1:p.Val704del
XM_011532664.1:c.2276_2278del	XP_011530966.1:p.Val759del
XM_011532665.1:c.1820_1822del	XP_011530967.1:p.Val607del
XM_011532666.1:c.1748_1750del	XP_011530968.1:p.Val583del
XM_011532667.1:c.1607_1609del	XP_011530969.1:p.Val536del
XM_011532668.1:c.2276_2278del	XP_011530970.1:p.Val759del
NM_001320893.1:c.1820_1822del	NP_001307822.1:p.Val607del
NR_135490.1:n.2614_2616del
XM_005264175.5:c.2276_2278del	XP_005264232.1:p.Val759del
XM_005264177.4:c.1607_1609del	XP_005264234.1:p.Val536del
XM_011532662.2:c.2129_2131del	XP_011530964.1:p.Val710del
XM_011532663.2:c.2111_2113del	XP_011530965.1:p.Val704del
XM_011532664.2:c.2276_2278del	XP_011530966.1:p.Val759del
XM_011532666.2:c.1748_1750del	XP_011530968.1:p.Val583del
XM_011532667.3:c.1607_1609del	XP_011530969.1:p.Val536del
XM_017003526.1:c.2276_2278del	XP_016859015.1:p.Val759del
XM_017003527.1:c.1607_1609del	XP_016859016.1:p.Val536del
XR_001738657.1:n.2553_2555del
NM_001375819.1:c.1607_1609del	NP_001362748.1:p.Val536del
NR_135490.2:n.2507_2509del
NM_022552.5:c.2276_2278del MANE Select	NP_072046.2:p.Val759del