Canonical Allele Identifier: CA1239254638

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234387_25234397delinsGACGTCAGTAT , CM000664.2:g.25234387_25234397delinsGACGTCAGTAT	GRCh38
NC_000002.11:g.25457256_25457266delinsGACGTCAGTAT , CM000664.1:g.25457256_25457266delinsGACGTCAGTAT	GRCh37
NC_000002.10:g.25310760_25310770delinsGACGTCAGTAT	NCBI36
NG_029465.2:g.113194_113204delinsATACTGACGTC , LRG_459:g.113194_113204delinsATACTGACGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.870_880delinsATACTGACGTC
ENST00000683393.1:c.1767_1777delinsATACTGACGTC	ENSP00000508654.1:n.1767_1777delinsATACTGACGTC
ENST00000683760.1:c.1952_1962delinsATACTGACGTC	ENSP00000507765.1:p.Tyr651=
ENST00000321117.10:c.2621_2631delinsATACTGACGTC MANE Select	ENSP00000324375.5:p.Tyr874=
ENST00000264709.7:c.2621_2631delinsATACTGACGTC	ENSP00000264709.3:p.Tyr874=
ENST00000321117.9:c.2621_2631delinsATACTGACGTC	ENSP00000324375.5:p.Tyr874=
ENST00000380746.8:c.2054_2064delinsATACTGACGTC	ENSP00000370122.4:p.Tyr685=
ENST00000380756.7:c.*474_*484delinsATACTGACGTC	ENSP00000370132.3:n.*474_*484delinsATACTGACGTC
ENST00000402667.1:c.1952_1962delinsATACTGACGTC	ENSP00000384237.1:p.Tyr651=
NM_022552.4:c.2621_2631delinsATACTGACGTC , LRG_459t1:c.2621_2631delinsATACTGACGTC	NP_072046.2:p.Tyr874=
NM_153759.3:c.2054_2064delinsATACTGACGTC , LRG_459t2:c.2054_2064delinsATACTGACGTC	NP_715640.2:p.Tyr685=
NM_175629.2:c.2621_2631delinsATACTGACGTC , LRG_459t4:c.2621_2631delinsATACTGACGTC	NP_783328.1:p.Tyr874=
XM_005264175.3:c.2621_2631delinsATACTGACGTC	XP_005264232.1:p.Tyr874=
XM_005264177.3:c.1952_1962delinsATACTGACGTC	XP_005264234.1:p.Tyr651=
XM_006711958.2:c.2177_2187delinsATACTGACGTC	XP_006712021.1:p.Tyr726=
XM_011532662.1:c.2474_2484delinsATACTGACGTC	XP_011530964.1:p.Tyr825=
XM_011532663.1:c.2456_2466delinsATACTGACGTC	XP_011530965.1:p.Tyr819=
XM_011532665.1:c.2165_2175delinsATACTGACGTC	XP_011530967.1:p.Tyr722=
XM_011532666.1:c.2093_2103delinsATACTGACGTC	XP_011530968.1:p.Tyr698=
XM_011532667.1:c.1952_1962delinsATACTGACGTC	XP_011530969.1:p.Tyr651=
NM_001320893.1:c.2165_2175delinsATACTGACGTC	NP_001307822.1:p.Tyr722=
NR_135490.1:n.3158_3168delinsATACTGACGTC
XM_005264175.5:c.2621_2631delinsATACTGACGTC	XP_005264232.1:p.Tyr874=
XM_005264177.4:c.1952_1962delinsATACTGACGTC	XP_005264234.1:p.Tyr651=
XM_011532662.2:c.2474_2484delinsATACTGACGTC	XP_011530964.1:p.Tyr825=
XM_011532663.2:c.2456_2466delinsATACTGACGTC	XP_011530965.1:p.Tyr819=
XM_011532666.2:c.2093_2103delinsATACTGACGTC	XP_011530968.1:p.Tyr698=
XM_011532667.3:c.1952_1962delinsATACTGACGTC	XP_011530969.1:p.Tyr651=
XM_017003526.1:c.2621_2631delinsATACTGACGTC	XP_016859015.1:p.Tyr874=
XM_017003527.1:c.1952_1962delinsATACTGACGTC	XP_016859016.1:p.Tyr651=
XR_001738657.1:n.2828_2838delinsATACTGACGTC
NM_001375819.1:c.1952_1962delinsATACTGACGTC	NP_001362748.1:p.Tyr651=
NR_135490.2:n.3051_3061delinsATACTGACGTC
NM_022552.5:c.2621_2631delinsATACTGACGTC MANE Select	NP_072046.2:p.Tyr874=