Canonical Allele Identifier: CA1239260198

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234223_25234227delinsGTTTT , CM000664.2:g.25234223_25234227delinsGTTTT	GRCh38
NC_000002.11:g.25457092_25457096delinsGTTTT , CM000664.1:g.25457092_25457096delinsGTTTT	GRCh37
NC_000002.10:g.25310596_25310600delinsGTTTT	NCBI36
NG_029465.2:g.113364_113368delinsAAAAC , LRG_459:g.113364_113368delinsAAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683393.1:c.1937_1941delinsAAAAC	ENSP00000508654.1:n.1937_1941delinsAAAAC
ENST00000683760.1:c.*52_*56delinsAAAAC	ENSP00000507765.1:n.*52_*56delinsAAAAC
ENST00000321117.10:c.*52_*56delinsAAAAC MANE Select	ENSP00000324375.5:n.*52_*56delinsAAAAC
ENST00000264709.7:c.*52_*56delinsAAAAC	ENSP00000264709.3:n.*52_*56delinsAAAAC
ENST00000321117.9:c.*52_*56delinsAAAAC	ENSP00000324375.5:n.*52_*56delinsAAAAC
ENST00000380746.8:c.*52_*56delinsAAAAC	ENSP00000370122.4:n.*52_*56delinsAAAAC
ENST00000380756.7:c.*644_*648delinsAAAAC	ENSP00000370132.3:n.*644_*648delinsAAAAC
ENST00000402667.1:c.*52_*56delinsAAAAC	ENSP00000384237.1:n.*52_*56delinsAAAAC
NM_022552.4:c.*52_*56delinsAAAAC , LRG_459t1:c.*52_*56delinsAAAAC	NP_072046.2:n.*52_*56delinsAAAAC
NM_153759.3:c.*52_*56delinsAAAAC , LRG_459t2:c.*52_*56delinsAAAAC	NP_715640.2:n.*52_*56delinsAAAAC
NM_175629.2:c.*52_*56delinsAAAAC , LRG_459t4:c.*52_*56delinsAAAAC	NP_783328.1:n.*52_*56delinsAAAAC
XM_005264175.3:c.*52_*56delinsAAAAC	XP_005264232.1:n.*52_*56delinsAAAAC
XM_005264177.3:c.*52_*56delinsAAAAC	XP_005264234.1:n.*52_*56delinsAAAAC
XM_006711958.2:c.*52_*56delinsAAAAC	XP_006712021.1:n.*52_*56delinsAAAAC
XM_011532662.1:c.*52_*56delinsAAAAC	XP_011530964.1:n.*52_*56delinsAAAAC
XM_011532663.1:c.*52_*56delinsAAAAC	XP_011530965.1:n.*52_*56delinsAAAAC
XM_011532665.1:c.*52_*56delinsAAAAC	XP_011530967.1:n.*52_*56delinsAAAAC
XM_011532666.1:c.*52_*56delinsAAAAC	XP_011530968.1:n.*52_*56delinsAAAAC
XM_011532667.1:c.*52_*56delinsAAAAC	XP_011530969.1:n.*52_*56delinsAAAAC
NM_001320893.1:c.*52_*56delinsAAAAC	NP_001307822.1:n.*52_*56delinsAAAAC
NR_135490.1:n.3328_3332delinsAAAAC
XM_005264175.5:c.*52_*56delinsAAAAC	XP_005264232.1:n.*52_*56delinsAAAAC
XM_005264177.4:c.*52_*56delinsAAAAC	XP_005264234.1:n.*52_*56delinsAAAAC
XM_011532662.2:c.*52_*56delinsAAAAC	XP_011530964.1:n.*52_*56delinsAAAAC
XM_011532663.2:c.*52_*56delinsAAAAC	XP_011530965.1:n.*52_*56delinsAAAAC
XM_011532666.2:c.*52_*56delinsAAAAC	XP_011530968.1:n.*52_*56delinsAAAAC
XM_011532667.3:c.*52_*56delinsAAAAC	XP_011530969.1:n.*52_*56delinsAAAAC
XM_017003526.1:c.*52_*56delinsAAAAC	XP_016859015.1:n.*52_*56delinsAAAAC
XM_017003527.1:c.*52_*56delinsAAAAC	XP_016859016.1:n.*52_*56delinsAAAAC
XR_001738657.1:n.2998_3002delinsAAAAC
NM_001375819.1:c.*52_*56delinsAAAAC	NP_001362748.1:n.*52_*56delinsAAAAC
NR_135490.2:n.3221_3225delinsAAAAC
NM_022552.5:c.*52_*56delinsAAAAC MANE Select	NP_072046.2:n.*52_*56delinsAAAAC