Canonical Allele Identifier: CA2658168855

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244285-GCCTGGGCAGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244288_25244297del , CM000664.2:g.25244288_25244297del	GRCh38
NC_000002.11:g.25467157_25467166del , CM000664.1:g.25467157_25467166del	GRCh37
NC_000002.10:g.25320661_25320670del	NCBI36
NG_029465.2:g.103296_103305del , LRG_459:g.103296_103305del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.30_39del
ENST00000683393.1:c.857_866del	ENSP00000508654.1:n.857_866del
ENST00000683760.1:c.1042_1051del	ENSP00000507765.1:p.Ala348GlnfsTer?
ENST00000321117.10:c.1711_1720del MANE Select	ENSP00000324375.5:p.Ala571GlnfsTer?
ENST00000264709.7:c.1711_1720del	ENSP00000264709.3:p.Ala571GlnfsTer?
ENST00000321117.9:c.1711_1720del	ENSP00000324375.5:p.Ala571GlnfsTer?
ENST00000380746.8:c.1144_1153del	ENSP00000370122.4:p.Ala382GlnfsTer?
ENST00000380756.7:c.1711_1720del	ENSP00000370132.3:p.Ala571GlnfsTer?
ENST00000402667.1:c.1042_1051del	ENSP00000384237.1:p.Ala348GlnfsTer?
ENST00000474887.5:n.30_39del
NM_022552.4:c.1711_1720del , LRG_459t1:c.1711_1720del	NP_072046.2:p.Ala571GlnfsTer?
NM_153759.3:c.1144_1153del , LRG_459t2:c.1144_1153del	NP_715640.2:p.Ala382GlnfsTer?
NM_175629.2:c.1711_1720del , LRG_459t4:c.1711_1720del	NP_783328.1:p.Ala571GlnfsTer?
XM_005264175.3:c.1711_1720del	XP_005264232.1:p.Ala571GlnfsTer?
XM_005264177.3:c.1042_1051del	XP_005264234.1:p.Ala348GlnfsTer?
XM_006711957.2:c.1711_1720del	XP_006712020.1:p.Ala571GlnfsTer?
XM_006711958.2:c.1267_1276del	XP_006712021.1:p.Ala423GlnfsTer?
XM_011532662.1:c.1564_1573del	XP_011530964.1:p.Ala522GlnfsTer?
XM_011532663.1:c.1546_1555del	XP_011530965.1:p.Ala516GlnfsTer?
XM_011532664.1:c.1711_1720del	XP_011530966.1:p.Ala571GlnfsTer?
XM_011532665.1:c.1255_1264del	XP_011530967.1:p.Ala419GlnfsTer?
XM_011532666.1:c.1183_1192del	XP_011530968.1:p.Ala395GlnfsTer?
XM_011532667.1:c.1042_1051del	XP_011530969.1:p.Ala348GlnfsTer?
XM_011532668.1:c.1711_1720del	XP_011530970.1:p.Ala571GlnfsTer?
NM_001320893.1:c.1255_1264del	NP_001307822.1:p.Ala419GlnfsTer?
NR_135490.1:n.2049_2058del
XM_005264175.5:c.1711_1720del	XP_005264232.1:p.Ala571GlnfsTer?
XM_005264177.4:c.1042_1051del	XP_005264234.1:p.Ala348GlnfsTer?
XM_011532662.2:c.1564_1573del	XP_011530964.1:p.Ala522GlnfsTer?
XM_011532663.2:c.1546_1555del	XP_011530965.1:p.Ala516GlnfsTer?
XM_011532664.2:c.1711_1720del	XP_011530966.1:p.Ala571GlnfsTer?
XM_011532666.2:c.1183_1192del	XP_011530968.1:p.Ala395GlnfsTer?
XM_011532667.3:c.1042_1051del	XP_011530969.1:p.Ala348GlnfsTer?
XM_017003526.1:c.1711_1720del	XP_016859015.1:p.Ala571GlnfsTer?
XM_017003527.1:c.1042_1051del	XP_016859016.1:p.Ala348GlnfsTer?
XR_001738657.1:n.1988_1997del
NM_001375819.1:c.1042_1051del	NP_001362748.1:p.Ala348GlnfsTer?
NR_135490.2:n.1942_1951del
NM_022552.5:c.1711_1720del MANE Select	NP_072046.2:p.Ala571GlnfsTer?