Canonical Allele Identifier: CA1239260263

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234312_25234313delinsGA , CM000664.2:g.25234312_25234313delinsGA	GRCh38
NC_000002.11:g.25457181_25457182delinsGA , CM000664.1:g.25457181_25457182delinsGA	GRCh37
NC_000002.10:g.25310685_25310686delinsGA	NCBI36
NG_029465.2:g.113278_113279delinsTC , LRG_459:g.113278_113279delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.954_955delinsTC
ENST00000683393.1:c.1851_1852delinsTC	ENSP00000508654.1:n.1851_1852delinsTC
ENST00000683760.1:c.2036_2037delinsTC	ENSP00000507765.1:p.Phe679=
ENST00000321117.10:c.2705_2706delinsTC MANE Select	ENSP00000324375.5:p.Phe902=
ENST00000264709.7:c.2705_2706delinsTC	ENSP00000264709.3:p.Phe902=
ENST00000321117.9:c.2705_2706delinsTC	ENSP00000324375.5:p.Phe902=
ENST00000380746.8:c.2138_2139delinsTC	ENSP00000370122.4:p.Phe713=
ENST00000380756.7:c.*558_*559delinsTC	ENSP00000370132.3:n.*558_*559delinsTC
ENST00000402667.1:c.2036_2037delinsTC	ENSP00000384237.1:p.Phe679=
NM_022552.4:c.2705_2706delinsTC , LRG_459t1:c.2705_2706delinsTC	NP_072046.2:p.Phe902=
NM_153759.3:c.2138_2139delinsTC , LRG_459t2:c.2138_2139delinsTC	NP_715640.2:p.Phe713=
NM_175629.2:c.2705_2706delinsTC , LRG_459t4:c.2705_2706delinsTC	NP_783328.1:p.Phe902=
XM_005264175.3:c.2705_2706delinsTC	XP_005264232.1:p.Phe902=
XM_005264177.3:c.2036_2037delinsTC	XP_005264234.1:p.Phe679=
XM_006711958.2:c.2261_2262delinsTC	XP_006712021.1:p.Phe754=
XM_011532662.1:c.2558_2559delinsTC	XP_011530964.1:p.Phe853=
XM_011532663.1:c.2540_2541delinsTC	XP_011530965.1:p.Phe847=
XM_011532665.1:c.2249_2250delinsTC	XP_011530967.1:p.Phe750=
XM_011532666.1:c.2177_2178delinsTC	XP_011530968.1:p.Phe726=
XM_011532667.1:c.2036_2037delinsTC	XP_011530969.1:p.Phe679=
NM_001320893.1:c.2249_2250delinsTC	NP_001307822.1:p.Phe750=
NR_135490.1:n.3242_3243delinsTC
XM_005264175.5:c.2705_2706delinsTC	XP_005264232.1:p.Phe902=
XM_005264177.4:c.2036_2037delinsTC	XP_005264234.1:p.Phe679=
XM_011532662.2:c.2558_2559delinsTC	XP_011530964.1:p.Phe853=
XM_011532663.2:c.2540_2541delinsTC	XP_011530965.1:p.Phe847=
XM_011532666.2:c.2177_2178delinsTC	XP_011530968.1:p.Phe726=
XM_011532667.3:c.2036_2037delinsTC	XP_011530969.1:p.Phe679=
XM_017003526.1:c.2705_2706delinsTC	XP_016859015.1:p.Phe902=
XM_017003527.1:c.2036_2037delinsTC	XP_016859016.1:p.Phe679=
XR_001738657.1:n.2912_2913delinsTC
NM_001375819.1:c.2036_2037delinsTC	NP_001362748.1:p.Phe679=
NR_135490.2:n.3135_3136delinsTC
NM_022552.5:c.2705_2706delinsTC MANE Select	NP_072046.2:p.Phe902=