Canonical Allele Identifier: CA645515178

Gene: DNMT3A

Linked Data

• COSMIC: COSM5611252 ; COSM5611253

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240395_25240396delinsAA , CM000664.2:g.25240395_25240396delinsAA	GRCh38
NC_000002.11:g.25463264_25463265delinsAA , CM000664.1:g.25463264_25463265delinsAA	GRCh37
NC_000002.10:g.25316768_25316769delinsAA	NCBI36
NG_029465.2:g.107195_107196delinsTT , LRG_459:g.107195_107196delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.547_548delinsTT
ENST00000683393.1:c.1374_1375delinsTT	ENSP00000508654.1:n.1374_1375delinsTT
ENST00000683760.1:c.1559_1560delinsTT	ENSP00000507765.1:p.Pro520Leu
ENST00000321117.10:c.2228_2229delinsTT MANE Select	ENSP00000324375.5:p.Pro743Leu
ENST00000264709.7:c.2228_2229delinsTT	ENSP00000264709.3:p.Pro743Leu
ENST00000321117.9:c.2228_2229delinsTT	ENSP00000324375.5:p.Pro743Leu
ENST00000380746.8:c.1661_1662delinsTT	ENSP00000370122.4:p.Pro554Leu
ENST00000380756.7:c.2228_2229delinsTT	ENSP00000370132.3:p.Pro743Leu
ENST00000402667.1:c.1559_1560delinsTT	ENSP00000384237.1:p.Pro520Leu
ENST00000461228.1:n.447_448delinsTT
ENST00000466601.5:n.600_601delinsTT
ENST00000474887.5:n.547_548delinsTT
ENST00000482935.5:n.228_229delinsTT
ENST00000491288.5:n.310+244_310+245delinsTT
NM_022552.4:c.2228_2229delinsTT , LRG_459t1:c.2228_2229delinsTT	NP_072046.2:p.Pro743Leu
NM_153759.3:c.1661_1662delinsTT , LRG_459t2:c.1661_1662delinsTT	NP_715640.2:p.Pro554Leu
NM_175629.2:c.2228_2229delinsTT , LRG_459t4:c.2228_2229delinsTT	NP_783328.1:p.Pro743Leu
XM_005264175.3:c.2228_2229delinsTT	XP_005264232.1:p.Pro743Leu
XM_005264177.3:c.1559_1560delinsTT	XP_005264234.1:p.Pro520Leu
XM_006711957.2:c.2228_2229delinsTT	XP_006712020.1:p.Pro743Leu
XM_006711958.2:c.1784_1785delinsTT	XP_006712021.1:p.Pro595Leu
XM_011532662.1:c.2081_2082delinsTT	XP_011530964.1:p.Pro694Leu
XM_011532663.1:c.2063_2064delinsTT	XP_011530965.1:p.Pro688Leu
XM_011532664.1:c.2228_2229delinsTT	XP_011530966.1:p.Pro743Leu
XM_011532665.1:c.1772_1773delinsTT	XP_011530967.1:p.Pro591Leu
XM_011532666.1:c.1700_1701delinsTT	XP_011530968.1:p.Pro567Leu
XM_011532667.1:c.1559_1560delinsTT	XP_011530969.1:p.Pro520Leu
XM_011532668.1:c.2228_2229delinsTT	XP_011530970.1:p.Pro743Leu
NM_001320893.1:c.1772_1773delinsTT	NP_001307822.1:p.Pro591Leu
NR_135490.1:n.2566_2567delinsTT
XM_005264175.5:c.2228_2229delinsTT	XP_005264232.1:p.Pro743Leu
XM_005264177.4:c.1559_1560delinsTT	XP_005264234.1:p.Pro520Leu
XM_011532662.2:c.2081_2082delinsTT	XP_011530964.1:p.Pro694Leu
XM_011532663.2:c.2063_2064delinsTT	XP_011530965.1:p.Pro688Leu
XM_011532664.2:c.2228_2229delinsTT	XP_011530966.1:p.Pro743Leu
XM_011532666.2:c.1700_1701delinsTT	XP_011530968.1:p.Pro567Leu
XM_011532667.3:c.1559_1560delinsTT	XP_011530969.1:p.Pro520Leu
XM_017003526.1:c.2228_2229delinsTT	XP_016859015.1:p.Pro743Leu
XM_017003527.1:c.1559_1560delinsTT	XP_016859016.1:p.Pro520Leu
XR_001738657.1:n.2505_2506delinsTT
NM_001375819.1:c.1559_1560delinsTT	NP_001362748.1:p.Pro520Leu
NR_135490.2:n.2459_2460delinsTT
NM_022552.5:c.2228_2229delinsTT MANE Select	NP_072046.2:p.Pro743Leu