Canonical Allele Identifier: CA1239264852
Gene: DNMT3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25240053_25240057delinsGTCCT , CM000664.2:g.25240053_25240057delinsGTCCT GRCh38
NC_000002.11:g.25462922_25462926delinsGTCCT , CM000664.1:g.25462922_25462926delinsGTCCT GRCh37
NC_000002.10:g.25316426_25316430delinsGTCCT NCBI36
NG_029465.2:g.107534_107538delinsAGGAC , LRG_459:g.107534_107538delinsAGGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.641+245_641+249delinsAGGAC
ENST00000683393.1:c.1468+245_1468+249delinsAGGAC ENSP00000508654.1:n.1468+245_1468+249delinsAGGAC
ENST00000683760.1:c.1653+245_1653+249delinsAGGAC ENSP00000507765.1:n.1653+245_1653+249delinsAGGAC
ENST00000321117.10:c.2322+245_2322+249delinsAGGAC MANE Select ENSP00000324375.5:n.2322+245_2322+249delinsAGGAC
ENST00000264709.7:c.2322+245_2322+249delinsAGGAC ENSP00000264709.3:n.2322+245_2322+249delinsAGGAC
ENST00000321117.9:c.2322+245_2322+249delinsAGGAC ENSP00000324375.5:n.2322+245_2322+249delinsAGGAC
ENST00000380746.8:c.1755+245_1755+249delinsAGGAC ENSP00000370122.4:n.1755+245_1755+249delinsAGGAC
ENST00000380756.7:c.2322+245_2322+249delinsAGGAC ENSP00000370132.3:n.2322+245_2322+249delinsAGGAC
ENST00000402667.1:c.1653+245_1653+249delinsAGGAC ENSP00000384237.1:n.1653+245_1653+249delinsAGGAC
ENST00000461228.1:n.541+245_541+249delinsAGGAC
ENST00000466601.5:n.694+245_694+249delinsAGGAC
ENST00000474887.5:n.641+245_641+249delinsAGGAC
ENST00000482935.5:n.322+245_322+249delinsAGGAC
ENST00000491288.5:n.310+583_310+587delinsAGGAC
NM_022552.4:c.2322+245_2322+249delinsAGGAC , LRG_459t1:c.2322+245_2322+249delinsAGGAC NP_072046.2:n.2322+245_2322+249delinsAGGAC
NM_153759.3:c.1755+245_1755+249delinsAGGAC , LRG_459t2:c.1755+245_1755+249delinsAGGAC NP_715640.2:n.1755+245_1755+249delinsAGGAC
NM_175629.2:c.2322+245_2322+249delinsAGGAC , LRG_459t4:c.2322+245_2322+249delinsAGGAC NP_783328.1:n.2322+245_2322+249delinsAGGAC
XM_005264175.3:c.2322+245_2322+249delinsAGGAC XP_005264232.1:n.2322+245_2322+249delinsAGGAC
XM_005264177.3:c.1653+245_1653+249delinsAGGAC XP_005264234.1:n.1653+245_1653+249delinsAGGAC
XM_006711957.2:c.2322+245_2322+249delinsAGGAC XP_006712020.1:n.2322+245_2322+249delinsAGGAC
XM_006711958.2:c.1878+245_1878+249delinsAGGAC XP_006712021.1:n.1878+245_1878+249delinsAGGAC
XM_011532662.1:c.2175+245_2175+249delinsAGGAC XP_011530964.1:n.2175+245_2175+249delinsAGGAC
XM_011532663.1:c.2157+245_2157+249delinsAGGAC XP_011530965.1:n.2157+245_2157+249delinsAGGAC
XM_011532664.1:c.2322+245_2322+249delinsAGGAC XP_011530966.1:n.2322+245_2322+249delinsAGGAC
XM_011532665.1:c.1866+245_1866+249delinsAGGAC XP_011530967.1:n.1866+245_1866+249delinsAGGAC
XM_011532666.1:c.1794+245_1794+249delinsAGGAC XP_011530968.1:n.1794+245_1794+249delinsAGGAC
XM_011532667.1:c.1653+245_1653+249delinsAGGAC XP_011530969.1:n.1653+245_1653+249delinsAGGAC
XM_011532668.1:c.2322+245_2322+249delinsAGGAC XP_011530970.1:n.2322+245_2322+249delinsAGGAC
NM_001320893.1:c.1866+245_1866+249delinsAGGAC NP_001307822.1:n.1866+245_1866+249delinsAGGAC
NR_135490.1:n.2660+245_2660+249delinsAGGAC
XM_005264175.5:c.2322+245_2322+249delinsAGGAC XP_005264232.1:n.2322+245_2322+249delinsAGGAC
XM_005264177.4:c.1653+245_1653+249delinsAGGAC XP_005264234.1:n.1653+245_1653+249delinsAGGAC
XM_011532662.2:c.2175+245_2175+249delinsAGGAC XP_011530964.1:n.2175+245_2175+249delinsAGGAC
XM_011532663.2:c.2157+245_2157+249delinsAGGAC XP_011530965.1:n.2157+245_2157+249delinsAGGAC
XM_011532664.2:c.2322+245_2322+249delinsAGGAC XP_011530966.1:n.2322+245_2322+249delinsAGGAC
XM_011532666.2:c.1794+245_1794+249delinsAGGAC XP_011530968.1:n.1794+245_1794+249delinsAGGAC
XM_011532667.3:c.1653+245_1653+249delinsAGGAC XP_011530969.1:n.1653+245_1653+249delinsAGGAC
XM_017003526.1:c.2322+245_2322+249delinsAGGAC XP_016859015.1:n.2322+245_2322+249delinsAGGAC
XM_017003527.1:c.1653+245_1653+249delinsAGGAC XP_016859016.1:n.1653+245_1653+249delinsAGGAC
XR_001738657.1:n.2599+245_2599+249delinsAGGAC
NM_001375819.1:c.1653+245_1653+249delinsAGGAC NP_001362748.1:n.1653+245_1653+249delinsAGGAC
NR_135490.2:n.2553+245_2553+249delinsAGGAC
NM_022552.5:c.2322+245_2322+249delinsAGGAC MANE Select NP_072046.2:n.2322+245_2322+249delinsAGGAC