Canonical Allele Identifier: CA1239265153

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240326_25240328delinsCTT , CM000664.2:g.25240326_25240328delinsCTT	GRCh38
NC_000002.11:g.25463195_25463197delinsCTT , CM000664.1:g.25463195_25463197delinsCTT	GRCh37
NC_000002.10:g.25316699_25316701delinsCTT	NCBI36
NG_029465.2:g.107263_107265delinsAAG , LRG_459:g.107263_107265delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.615_617delinsAAG
ENST00000683393.1:c.1442_1444delinsAAG	ENSP00000508654.1:n.1442_1444delinsAAG
ENST00000683760.1:c.1627_1629delinsAAG	ENSP00000507765.1:p.Lys543=
ENST00000321117.10:c.2296_2298delinsAAG MANE Select	ENSP00000324375.5:p.Lys766=
ENST00000264709.7:c.2296_2298delinsAAG	ENSP00000264709.3:p.Lys766=
ENST00000321117.9:c.2296_2298delinsAAG	ENSP00000324375.5:p.Lys766=
ENST00000380746.8:c.1729_1731delinsAAG	ENSP00000370122.4:p.Lys577=
ENST00000380756.7:c.2296_2298delinsAAG	ENSP00000370132.3:p.Lys766=
ENST00000402667.1:c.1627_1629delinsAAG	ENSP00000384237.1:p.Lys543=
ENST00000461228.1:n.515_517delinsAAG
ENST00000466601.5:n.668_670delinsAAG
ENST00000474887.5:n.615_617delinsAAG
ENST00000482935.5:n.296_298delinsAAG
ENST00000491288.5:n.310+312_310+314delinsAAG
NM_022552.4:c.2296_2298delinsAAG , LRG_459t1:c.2296_2298delinsAAG	NP_072046.2:p.Lys766=
NM_153759.3:c.1729_1731delinsAAG , LRG_459t2:c.1729_1731delinsAAG	NP_715640.2:p.Lys577=
NM_175629.2:c.2296_2298delinsAAG , LRG_459t4:c.2296_2298delinsAAG	NP_783328.1:p.Lys766=
XM_005264175.3:c.2296_2298delinsAAG	XP_005264232.1:p.Lys766=
XM_005264177.3:c.1627_1629delinsAAG	XP_005264234.1:p.Lys543=
XM_006711957.2:c.2296_2298delinsAAG	XP_006712020.1:p.Lys766=
XM_006711958.2:c.1852_1854delinsAAG	XP_006712021.1:p.Lys618=
XM_011532662.1:c.2149_2151delinsAAG	XP_011530964.1:p.Lys717=
XM_011532663.1:c.2131_2133delinsAAG	XP_011530965.1:p.Lys711=
XM_011532664.1:c.2296_2298delinsAAG	XP_011530966.1:p.Lys766=
XM_011532665.1:c.1840_1842delinsAAG	XP_011530967.1:p.Lys614=
XM_011532666.1:c.1768_1770delinsAAG	XP_011530968.1:p.Lys590=
XM_011532667.1:c.1627_1629delinsAAG	XP_011530969.1:p.Lys543=
XM_011532668.1:c.2296_2298delinsAAG	XP_011530970.1:p.Lys766=
NM_001320893.1:c.1840_1842delinsAAG	NP_001307822.1:p.Lys614=
NR_135490.1:n.2634_2636delinsAAG
XM_005264175.5:c.2296_2298delinsAAG	XP_005264232.1:p.Lys766=
XM_005264177.4:c.1627_1629delinsAAG	XP_005264234.1:p.Lys543=
XM_011532662.2:c.2149_2151delinsAAG	XP_011530964.1:p.Lys717=
XM_011532663.2:c.2131_2133delinsAAG	XP_011530965.1:p.Lys711=
XM_011532664.2:c.2296_2298delinsAAG	XP_011530966.1:p.Lys766=
XM_011532666.2:c.1768_1770delinsAAG	XP_011530968.1:p.Lys590=
XM_011532667.3:c.1627_1629delinsAAG	XP_011530969.1:p.Lys543=
XM_017003526.1:c.2296_2298delinsAAG	XP_016859015.1:p.Lys766=
XM_017003527.1:c.1627_1629delinsAAG	XP_016859016.1:p.Lys543=
XR_001738657.1:n.2573_2575delinsAAG
NM_001375819.1:c.1627_1629delinsAAG	NP_001362748.1:p.Lys543=
NR_135490.2:n.2527_2529delinsAAG
NM_022552.5:c.2296_2298delinsAAG MANE Select	NP_072046.2:p.Lys766=