Canonical Allele Identifier: CA2594345642
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25246628_25246633del , CM000664.2:g.25246628_25246633del GRCh38
NC_000002.11:g.25469497_25469502del , CM000664.1:g.25469497_25469502del GRCh37
NC_000002.10:g.25323001_25323006del NCBI36
NG_029465.2:g.100958_100963del , LRG_459:g.100958_100963del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683393.1:c.412_417del ENSP00000508654.1:n.412_417del
ENST00000683760.1:c.597_602del ENSP00000507765.1:p.Glu200_Pro201del
ENST00000321117.10:c.1266_1271del MANE Select ENSP00000324375.5:p.Glu423_Pro424del
ENST00000264709.7:c.1266_1271del ENSP00000264709.3:p.Glu423_Pro424del
ENST00000321117.9:c.1266_1271del ENSP00000324375.5:p.Glu423_Pro424del
ENST00000380746.8:c.699_704del ENSP00000370122.4:p.Glu234_Pro235del
ENST00000380756.7:c.1266_1271del ENSP00000370132.3:p.Glu423_Pro424del
ENST00000402667.1:c.597_602del ENSP00000384237.1:p.Glu200_Pro201del
ENST00000474807.5:n.561_566del
NM_022552.4:c.1266_1271del , LRG_459t1:c.1266_1271del NP_072046.2:p.Glu423_Pro424del
NM_153759.3:c.699_704del , LRG_459t2:c.699_704del NP_715640.2:p.Glu234_Pro235del
NM_175629.2:c.1266_1271del , LRG_459t4:c.1266_1271del NP_783328.1:p.Glu423_Pro424del
XM_005264175.3:c.1266_1271del XP_005264232.1:p.Glu423_Pro424del
XM_005264177.3:c.597_602del XP_005264234.1:p.Glu200_Pro201del
XM_006711957.2:c.1266_1271del XP_006712020.1:p.Glu423_Pro424del
XM_006711958.2:c.822_827del XP_006712021.1:p.Glu275_Pro276del
XM_011532662.1:c.1119_1124del XP_011530964.1:p.Glu374_Pro375del
XM_011532663.1:c.1101_1106del XP_011530965.1:p.Glu368_Pro369del
XM_011532664.1:c.1266_1271del XP_011530966.1:p.Glu423_Pro424del
XM_011532665.1:c.810_815del XP_011530967.1:p.Glu271_Pro272del
XM_011532666.1:c.738_743del XP_011530968.1:p.Glu247_Pro248del
XM_011532667.1:c.597_602del XP_011530969.1:p.Glu200_Pro201del
XM_011532668.1:c.1266_1271del XP_011530970.1:p.Glu423_Pro424del
NM_001320893.1:c.810_815del NP_001307822.1:p.Glu271_Pro272del
NR_135490.1:n.1604_1609del
XM_005264175.5:c.1266_1271del XP_005264232.1:p.Glu423_Pro424del
XM_005264177.4:c.597_602del XP_005264234.1:p.Glu200_Pro201del
XM_011532662.2:c.1119_1124del XP_011530964.1:p.Glu374_Pro375del
XM_011532663.2:c.1101_1106del XP_011530965.1:p.Glu368_Pro369del
XM_011532664.2:c.1266_1271del XP_011530966.1:p.Glu423_Pro424del
XM_011532666.2:c.738_743del XP_011530968.1:p.Glu247_Pro248del
XM_011532667.3:c.597_602del XP_011530969.1:p.Glu200_Pro201del
XM_017003526.1:c.1266_1271del XP_016859015.1:p.Glu423_Pro424del
XM_017003527.1:c.597_602del XP_016859016.1:p.Glu200_Pro201del
XR_001738657.1:n.1543_1548del
NM_001375819.1:c.597_602del NP_001362748.1:p.Glu200_Pro201del
NR_135490.2:n.1497_1502del
NM_022552.5:c.1266_1271del MANE Select NP_072046.2:p.Glu423_Pro424del