Canonical Allele Identifier: CA1239262924

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244264_25244270delinsCAGGGGT , CM000664.2:g.25244264_25244270delinsCAGGGGT	GRCh38
NC_000002.11:g.25467133_25467139delinsCAGGGGT , CM000664.1:g.25467133_25467139delinsCAGGGGT	GRCh37
NC_000002.10:g.25320637_25320643delinsCAGGGGT	NCBI36
NG_029465.2:g.103321_103327delinsACCCCTG , LRG_459:g.103321_103327delinsACCCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.55_61delinsACCCCTG
ENST00000683393.1:c.882_888delinsACCCCTG	ENSP00000508654.1:n.882_888delinsACCCCTG
ENST00000683760.1:c.1067_1073delinsACCCCTG	ENSP00000507765.1:p.Asp356=
ENST00000321117.10:c.1736_1742delinsACCCCTG MANE Select	ENSP00000324375.5:p.Asp579=
ENST00000264709.7:c.1736_1742delinsACCCCTG	ENSP00000264709.3:p.Asp579=
ENST00000321117.9:c.1736_1742delinsACCCCTG	ENSP00000324375.5:p.Asp579=
ENST00000380746.8:c.1169_1175delinsACCCCTG	ENSP00000370122.4:p.Asp390=
ENST00000380756.7:c.1736_1742delinsACCCCTG	ENSP00000370132.3:p.Asp579=
ENST00000402667.1:c.1067_1073delinsACCCCTG	ENSP00000384237.1:p.Asp356=
ENST00000474887.5:n.55_61delinsACCCCTG
NM_022552.4:c.1736_1742delinsACCCCTG , LRG_459t1:c.1736_1742delinsACCCCTG	NP_072046.2:p.Asp579=
NM_153759.3:c.1169_1175delinsACCCCTG , LRG_459t2:c.1169_1175delinsACCCCTG	NP_715640.2:p.Asp390=
NM_175629.2:c.1736_1742delinsACCCCTG , LRG_459t4:c.1736_1742delinsACCCCTG	NP_783328.1:p.Asp579=
XM_005264175.3:c.1736_1742delinsACCCCTG	XP_005264232.1:p.Asp579=
XM_005264177.3:c.1067_1073delinsACCCCTG	XP_005264234.1:p.Asp356=
XM_006711957.2:c.1736_1742delinsACCCCTG	XP_006712020.1:p.Asp579=
XM_006711958.2:c.1292_1298delinsACCCCTG	XP_006712021.1:p.Asp431=
XM_011532662.1:c.1589_1595delinsACCCCTG	XP_011530964.1:p.Asp530=
XM_011532663.1:c.1571_1577delinsACCCCTG	XP_011530965.1:p.Asp524=
XM_011532664.1:c.1736_1742delinsACCCCTG	XP_011530966.1:p.Asp579=
XM_011532665.1:c.1280_1286delinsACCCCTG	XP_011530967.1:p.Asp427=
XM_011532666.1:c.1208_1214delinsACCCCTG	XP_011530968.1:p.Asp403=
XM_011532667.1:c.1067_1073delinsACCCCTG	XP_011530969.1:p.Asp356=
XM_011532668.1:c.1736_1742delinsACCCCTG	XP_011530970.1:p.Asp579=
NM_001320893.1:c.1280_1286delinsACCCCTG	NP_001307822.1:p.Asp427=
NR_135490.1:n.2074_2080delinsACCCCTG
XM_005264175.5:c.1736_1742delinsACCCCTG	XP_005264232.1:p.Asp579=
XM_005264177.4:c.1067_1073delinsACCCCTG	XP_005264234.1:p.Asp356=
XM_011532662.2:c.1589_1595delinsACCCCTG	XP_011530964.1:p.Asp530=
XM_011532663.2:c.1571_1577delinsACCCCTG	XP_011530965.1:p.Asp524=
XM_011532664.2:c.1736_1742delinsACCCCTG	XP_011530966.1:p.Asp579=
XM_011532666.2:c.1208_1214delinsACCCCTG	XP_011530968.1:p.Asp403=
XM_011532667.3:c.1067_1073delinsACCCCTG	XP_011530969.1:p.Asp356=
XM_017003526.1:c.1736_1742delinsACCCCTG	XP_016859015.1:p.Asp579=
XM_017003527.1:c.1067_1073delinsACCCCTG	XP_016859016.1:p.Asp356=
XR_001738657.1:n.2013_2019delinsACCCCTG
NM_001375819.1:c.1067_1073delinsACCCCTG	NP_001362748.1:p.Asp356=
NR_135490.2:n.1967_1973delinsACCCCTG
NM_022552.5:c.1736_1742delinsACCCCTG MANE Select	NP_072046.2:p.Asp579=