Canonical Allele Identifier: CA2576694276

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244174_25244180del , CM000664.2:g.25244174_25244180del	GRCh38
NC_000002.11:g.25467043_25467049del , CM000664.1:g.25467043_25467049del	GRCh37
NC_000002.10:g.25320547_25320553del	NCBI36
NG_029465.2:g.103412_103418del , LRG_459:g.103412_103418del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.146_152del
ENST00000683393.1:c.973_979del	ENSP00000508654.1:n.973_979del
ENST00000683760.1:c.1158_1164del	ENSP00000507765.1:p.Phe386LeufsTer?
ENST00000321117.10:c.1827_1833del MANE Select	ENSP00000324375.5:p.Phe609LeufsTer?
ENST00000264709.7:c.1827_1833del	ENSP00000264709.3:p.Phe609LeufsTer?
ENST00000321117.9:c.1827_1833del	ENSP00000324375.5:p.Phe609LeufsTer?
ENST00000380746.8:c.1260_1266del	ENSP00000370122.4:p.Phe420LeufsTer?
ENST00000380756.7:c.1827_1833del	ENSP00000370132.3:p.Phe609LeufsTer?
ENST00000402667.1:c.1158_1164del	ENSP00000384237.1:p.Phe386LeufsTer?
ENST00000474887.5:n.146_152del
NM_022552.4:c.1827_1833del , LRG_459t1:c.1827_1833del	NP_072046.2:p.Phe609LeufsTer?
NM_153759.3:c.1260_1266del , LRG_459t2:c.1260_1266del	NP_715640.2:p.Phe420LeufsTer?
NM_175629.2:c.1827_1833del , LRG_459t4:c.1827_1833del	NP_783328.1:p.Phe609LeufsTer?
XM_005264175.3:c.1827_1833del	XP_005264232.1:p.Phe609LeufsTer?
XM_005264177.3:c.1158_1164del	XP_005264234.1:p.Phe386LeufsTer?
XM_006711957.2:c.1827_1833del	XP_006712020.1:p.Phe609LeufsTer?
XM_006711958.2:c.1383_1389del	XP_006712021.1:p.Phe461LeufsTer?
XM_011532662.1:c.1680_1686del	XP_011530964.1:p.Phe560LeufsTer?
XM_011532663.1:c.1662_1668del	XP_011530965.1:p.Phe554LeufsTer?
XM_011532664.1:c.1827_1833del	XP_011530966.1:p.Phe609LeufsTer?
XM_011532665.1:c.1371_1377del	XP_011530967.1:p.Phe457LeufsTer?
XM_011532666.1:c.1299_1305del	XP_011530968.1:p.Phe433LeufsTer?
XM_011532667.1:c.1158_1164del	XP_011530969.1:p.Phe386LeufsTer?
XM_011532668.1:c.1827_1833del	XP_011530970.1:p.Phe609LeufsTer?
NM_001320893.1:c.1371_1377del	NP_001307822.1:p.Phe457LeufsTer?
NR_135490.1:n.2165_2171del
XM_005264175.5:c.1827_1833del	XP_005264232.1:p.Phe609LeufsTer?
XM_005264177.4:c.1158_1164del	XP_005264234.1:p.Phe386LeufsTer?
XM_011532662.2:c.1680_1686del	XP_011530964.1:p.Phe560LeufsTer?
XM_011532663.2:c.1662_1668del	XP_011530965.1:p.Phe554LeufsTer?
XM_011532664.2:c.1827_1833del	XP_011530966.1:p.Phe609LeufsTer?
XM_011532666.2:c.1299_1305del	XP_011530968.1:p.Phe433LeufsTer?
XM_011532667.3:c.1158_1164del	XP_011530969.1:p.Phe386LeufsTer?
XM_017003526.1:c.1827_1833del	XP_016859015.1:p.Phe609LeufsTer?
XM_017003527.1:c.1158_1164del	XP_016859016.1:p.Phe386LeufsTer?
XR_001738657.1:n.2104_2110del
NM_001375819.1:c.1158_1164del	NP_001362748.1:p.Phe386LeufsTer?
NR_135490.2:n.2058_2064del
NM_022552.5:c.1827_1833del MANE Select	NP_072046.2:p.Phe609LeufsTer?