Canonical Allele Identifier: CA425181427

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25463218_25463219insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240349_25240350insT , CM000664.2:g.25240349_25240350insT	GRCh38
NC_000002.11:g.25463218_25463219insT , CM000664.1:g.25463218_25463219insT	GRCh37
NC_000002.10:g.25316722_25316723insT	NCBI36
NG_029465.2:g.107241_107242insA , LRG_459:g.107241_107242insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.593_594insA
ENST00000683393.1:c.1420_1421insA	ENSP00000508654.1:n.1420_1421insA
ENST00000683760.1:c.1605_1606insA	ENSP00000507765.1:p.Val536SerfsTer6
ENST00000321117.10:c.2274_2275insA MANE Select	ENSP00000324375.5:p.Val759SerfsTer6
ENST00000264709.7:c.2274_2275insA	ENSP00000264709.3:p.Val759SerfsTer6
ENST00000321117.9:c.2274_2275insA	ENSP00000324375.5:p.Val759SerfsTer6
ENST00000380746.8:c.1707_1708insA	ENSP00000370122.4:p.Val570SerfsTer6
ENST00000380756.7:c.2274_2275insA	ENSP00000370132.3:p.Val759SerfsTer6
ENST00000402667.1:c.1605_1606insA	ENSP00000384237.1:p.Val536SerfsTer6
ENST00000461228.1:n.493_494insA
ENST00000466601.5:n.646_647insA
ENST00000474887.5:n.593_594insA
ENST00000482935.5:n.274_275insA
ENST00000491288.5:n.310+290_310+291insA
NM_022552.4:c.2274_2275insA , LRG_459t1:c.2274_2275insA	NP_072046.2:p.Val759SerfsTer6
NM_153759.3:c.1707_1708insA , LRG_459t2:c.1707_1708insA	NP_715640.2:p.Val570SerfsTer6
NM_175629.2:c.2274_2275insA , LRG_459t4:c.2274_2275insA	NP_783328.1:p.Val759SerfsTer6
XM_005264175.3:c.2274_2275insA	XP_005264232.1:p.Val759SerfsTer6
XM_005264177.3:c.1605_1606insA	XP_005264234.1:p.Val536SerfsTer6
XM_006711957.2:c.2274_2275insA	XP_006712020.1:p.Val759SerfsTer6
XM_006711958.2:c.1830_1831insA	XP_006712021.1:p.Val611SerfsTer6
XM_011532662.1:c.2127_2128insA	XP_011530964.1:p.Val710SerfsTer6
XM_011532663.1:c.2109_2110insA	XP_011530965.1:p.Val704SerfsTer6
XM_011532664.1:c.2274_2275insA	XP_011530966.1:p.Val759SerfsTer6
XM_011532665.1:c.1818_1819insA	XP_011530967.1:p.Val607SerfsTer6
XM_011532666.1:c.1746_1747insA	XP_011530968.1:p.Val583SerfsTer6
XM_011532667.1:c.1605_1606insA	XP_011530969.1:p.Val536SerfsTer6
XM_011532668.1:c.2274_2275insA	XP_011530970.1:p.Val759SerfsTer6
NM_001320893.1:c.1818_1819insA	NP_001307822.1:p.Val607SerfsTer6
NR_135490.1:n.2612_2613insA
XM_005264175.5:c.2274_2275insA	XP_005264232.1:p.Val759SerfsTer6
XM_005264177.4:c.1605_1606insA	XP_005264234.1:p.Val536SerfsTer6
XM_011532662.2:c.2127_2128insA	XP_011530964.1:p.Val710SerfsTer6
XM_011532663.2:c.2109_2110insA	XP_011530965.1:p.Val704SerfsTer6
XM_011532664.2:c.2274_2275insA	XP_011530966.1:p.Val759SerfsTer6
XM_011532666.2:c.1746_1747insA	XP_011530968.1:p.Val583SerfsTer6
XM_011532667.3:c.1605_1606insA	XP_011530969.1:p.Val536SerfsTer6
XM_017003526.1:c.2274_2275insA	XP_016859015.1:p.Val759SerfsTer6
XM_017003527.1:c.1605_1606insA	XP_016859016.1:p.Val536SerfsTer6
XR_001738657.1:n.2551_2552insA
NM_001375819.1:c.1605_1606insA	NP_001362748.1:p.Val536SerfsTer6
NR_135490.2:n.2505_2506insA
NM_022552.5:c.2274_2275insA MANE Select	NP_072046.2:p.Val759SerfsTer6