Canonical Allele Identifier: CA2576694275

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244172_25244175del , CM000664.2:g.25244172_25244175del	GRCh38
NC_000002.11:g.25467041_25467044del , CM000664.1:g.25467041_25467044del	GRCh37
NC_000002.10:g.25320545_25320548del	NCBI36
NG_029465.2:g.103417_103420del , LRG_459:g.103417_103420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.151_154del
ENST00000683393.1:c.978_981del	ENSP00000508654.1:n.978_981del
ENST00000683760.1:c.1163_1166del	ENSP00000507765.1:p.Asn388ThrfsTer?
ENST00000321117.10:c.1832_1835del MANE Select	ENSP00000324375.5:p.Asn611ThrfsTer?
ENST00000264709.7:c.1832_1835del	ENSP00000264709.3:p.Asn611ThrfsTer?
ENST00000321117.9:c.1832_1835del	ENSP00000324375.5:p.Asn611ThrfsTer?
ENST00000380746.8:c.1265_1268del	ENSP00000370122.4:p.Asn422ThrfsTer?
ENST00000380756.7:c.1832_1835del	ENSP00000370132.3:p.Asn611ThrfsTer?
ENST00000402667.1:c.1163_1166del	ENSP00000384237.1:p.Asn388ThrfsTer?
ENST00000474887.5:n.151_154del
NM_022552.4:c.1832_1835del , LRG_459t1:c.1832_1835del	NP_072046.2:p.Asn611ThrfsTer?
NM_153759.3:c.1265_1268del , LRG_459t2:c.1265_1268del	NP_715640.2:p.Asn422ThrfsTer?
NM_175629.2:c.1832_1835del , LRG_459t4:c.1832_1835del	NP_783328.1:p.Asn611ThrfsTer?
XM_005264175.3:c.1832_1835del	XP_005264232.1:p.Asn611ThrfsTer?
XM_005264177.3:c.1163_1166del	XP_005264234.1:p.Asn388ThrfsTer?
XM_006711957.2:c.1832_1835del	XP_006712020.1:p.Asn611ThrfsTer?
XM_006711958.2:c.1388_1391del	XP_006712021.1:p.Asn463ThrfsTer?
XM_011532662.1:c.1685_1688del	XP_011530964.1:p.Asn562ThrfsTer?
XM_011532663.1:c.1667_1670del	XP_011530965.1:p.Asn556ThrfsTer?
XM_011532664.1:c.1832_1835del	XP_011530966.1:p.Asn611ThrfsTer?
XM_011532665.1:c.1376_1379del	XP_011530967.1:p.Asn459ThrfsTer?
XM_011532666.1:c.1304_1307del	XP_011530968.1:p.Asn435ThrfsTer?
XM_011532667.1:c.1163_1166del	XP_011530969.1:p.Asn388ThrfsTer?
XM_011532668.1:c.1832_1835del	XP_011530970.1:p.Asn611ThrfsTer?
NM_001320893.1:c.1376_1379del	NP_001307822.1:p.Asn459ThrfsTer?
NR_135490.1:n.2170_2173del
XM_005264175.5:c.1832_1835del	XP_005264232.1:p.Asn611ThrfsTer?
XM_005264177.4:c.1163_1166del	XP_005264234.1:p.Asn388ThrfsTer?
XM_011532662.2:c.1685_1688del	XP_011530964.1:p.Asn562ThrfsTer?
XM_011532663.2:c.1667_1670del	XP_011530965.1:p.Asn556ThrfsTer?
XM_011532664.2:c.1832_1835del	XP_011530966.1:p.Asn611ThrfsTer?
XM_011532666.2:c.1304_1307del	XP_011530968.1:p.Asn435ThrfsTer?
XM_011532667.3:c.1163_1166del	XP_011530969.1:p.Asn388ThrfsTer?
XM_017003526.1:c.1832_1835del	XP_016859015.1:p.Asn611ThrfsTer?
XM_017003527.1:c.1163_1166del	XP_016859016.1:p.Asn388ThrfsTer?
XR_001738657.1:n.2109_2112del
NM_001375819.1:c.1163_1166del	NP_001362748.1:p.Asn388ThrfsTer?
NR_135490.2:n.2063_2066del
NM_022552.5:c.1832_1835del MANE Select	NP_072046.2:p.Asn611ThrfsTer?