Canonical Allele Identifier: CA425181405

Gene: DNMT3A

Linked Data

• MyVariant Identifiers: chr2:g.25463186_25463187insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240317_25240318insT , CM000664.2:g.25240317_25240318insT	GRCh38
NC_000002.11:g.25463186_25463187insT , CM000664.1:g.25463186_25463187insT	GRCh37
NC_000002.10:g.25316690_25316691insT	NCBI36
NG_029465.2:g.107273_107274insA , LRG_459:g.107273_107274insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474887.6:c.625_626insA
ENST00000683393.1:c.1452_1453insA	ENSP00000508654.1:n.1452_1453insA
ENST00000683760.1:c.1637_1638insA	ENSP00000507765.1:p.Ser547LeufsTer12
ENST00000321117.10:c.2306_2307insA MANE Select	ENSP00000324375.5:p.Ser770LeufsTer12
ENST00000264709.7:c.2306_2307insA	ENSP00000264709.3:p.Ser770LeufsTer12
ENST00000321117.9:c.2306_2307insA	ENSP00000324375.5:p.Ser770LeufsTer12
ENST00000380746.8:c.1739_1740insA	ENSP00000370122.4:p.Ser581LeufsTer12
ENST00000380756.7:c.2306_2307insA	ENSP00000370132.3:p.Ser770LeufsTer9
ENST00000402667.1:c.1637_1638insA	ENSP00000384237.1:p.Ser547LeufsTer12
ENST00000461228.1:n.525_526insA
ENST00000466601.5:n.678_679insA
ENST00000474887.5:n.625_626insA
ENST00000482935.5:n.306_307insA
ENST00000491288.5:n.310+322_310+323insA
NM_022552.4:c.2306_2307insA , LRG_459t1:c.2306_2307insA	NP_072046.2:p.Ser770LeufsTer12
NM_153759.3:c.1739_1740insA , LRG_459t2:c.1739_1740insA	NP_715640.2:p.Ser581LeufsTer12
NM_175629.2:c.2306_2307insA , LRG_459t4:c.2306_2307insA	NP_783328.1:p.Ser770LeufsTer12
XM_005264175.3:c.2306_2307insA	XP_005264232.1:p.Ser770LeufsTer12
XM_005264177.3:c.1637_1638insA	XP_005264234.1:p.Ser547LeufsTer12
XM_006711957.2:c.2306_2307insA	XP_006712020.1:p.Ser770LeufsTer12
XM_006711958.2:c.1862_1863insA	XP_006712021.1:p.Ser622LeufsTer12
XM_011532662.1:c.2159_2160insA	XP_011530964.1:p.Ser721LeufsTer12
XM_011532663.1:c.2141_2142insA	XP_011530965.1:p.Ser715LeufsTer12
XM_011532664.1:c.2306_2307insA	XP_011530966.1:p.Ser770LeufsTer9
XM_011532665.1:c.1850_1851insA	XP_011530967.1:p.Ser618LeufsTer12
XM_011532666.1:c.1778_1779insA	XP_011530968.1:p.Ser594LeufsTer12
XM_011532667.1:c.1637_1638insA	XP_011530969.1:p.Ser547LeufsTer12
XM_011532668.1:c.2306_2307insA	XP_011530970.1:p.Ser770LeufsTer9
NM_001320893.1:c.1850_1851insA	NP_001307822.1:p.Ser618LeufsTer12
NR_135490.1:n.2644_2645insA
XM_005264175.5:c.2306_2307insA	XP_005264232.1:p.Ser770LeufsTer12
XM_005264177.4:c.1637_1638insA	XP_005264234.1:p.Ser547LeufsTer12
XM_011532662.2:c.2159_2160insA	XP_011530964.1:p.Ser721LeufsTer12
XM_011532663.2:c.2141_2142insA	XP_011530965.1:p.Ser715LeufsTer12
XM_011532664.2:c.2306_2307insA	XP_011530966.1:p.Ser770LeufsTer9
XM_011532666.2:c.1778_1779insA	XP_011530968.1:p.Ser594LeufsTer12
XM_011532667.3:c.1637_1638insA	XP_011530969.1:p.Ser547LeufsTer12
XM_017003526.1:c.2306_2307insA	XP_016859015.1:p.Ser770LeufsTer12
XM_017003527.1:c.1637_1638insA	XP_016859016.1:p.Ser547LeufsTer12
XR_001738657.1:n.2583_2584insA
NM_001375819.1:c.1637_1638insA	NP_001362748.1:p.Ser547LeufsTer12
NR_135490.2:n.2537_2538insA
NM_022552.5:c.2306_2307insA MANE Select	NP_072046.2:p.Ser770LeufsTer12