Canonical Allele Identifier: CA2652424140
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32808163_32808164insCAAGTTT , CM000682.2:g.32808163_32808164insCAAGTTT GRCh38
NC_000020.10:g.31395969_31395970insCAAGTTT , CM000682.1:g.31395969_31395970insCAAGTTT GRCh37
NC_000020.9:g.30859630_30859631insCAAGTTT NCBI36
NG_007290.1:g.50779_50780insCAAGTTT , LRG_56:g.50779_50780insCAAGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1773_*1774insCAAGTTT ENSP00000512497.1:n.*1773_*1774insCAAGTTT
ENST00000696232.1:c.*260_*261insCAAGTTT ENSP00000512498.1:n.*260_*261insCAAGTTT
ENST00000696233.1:c.*1376_*1377insCAAGTTT ENSP00000512499.1:n.*1376_*1377insCAAGTTT
ENST00000696238.1:c.*1565_*1566insCAAGTTT ENSP00000512502.1:n.*1565_*1566insCAAGTTT
ENST00000696245.1:n.847_848insCAAGTTT
ENST00000201963.3:c.*260_*261insCAAGTTT ENSP00000201963.3:n.*260_*261insCAAGTTT
ENST00000328111.6:c.*260_*261insCAAGTTT MANE Select ENSP00000328547.2:n.*260_*261insCAAGTTT
ENST00000348286.6:c.*260_*261insCAAGTTT ENSP00000337764.2:n.*260_*261insCAAGTTT
ENST00000353855.6:c.*260_*261insCAAGTTT ENSP00000313397.4:n.*260_*261insCAAGTTT
ENST00000443239.7:c.*260_*261insCAAGTTT ENSP00000403169.2:n.*260_*261insCAAGTTT
NM_001207055.1:c.*260_*261insCAAGTTT NP_001193984.1:n.*260_*261insCAAGTTT
NM_001207056.1:c.*260_*261insCAAGTTT NP_001193985.1:n.*260_*261insCAAGTTT
NM_006892.3:c.*260_*261insCAAGTTT , LRG_56t1:c.*260_*261insCAAGTTT NP_008823.1:n.*260_*261insCAAGTTT
NM_175848.1:c.*260_*261insCAAGTTT NP_787044.1:n.*260_*261insCAAGTTT
NM_175849.1:c.*260_*261insCAAGTTT NP_787045.1:n.*260_*261insCAAGTTT
NM_175850.2:c.*260_*261insCAAGTTT NP_787046.1:n.*260_*261insCAAGTTT
XM_011528653.1:c.*260_*261insCAAGTTT XP_011526955.1:n.*260_*261insCAAGTTT
XM_011528654.1:c.*260_*261insCAAGTTT XP_011526956.1:n.*260_*261insCAAGTTT
XR_936511.1:n.2600_2601insCAAGTTT
XM_011528653.2:c.*260_*261insCAAGTTT XP_011526955.1:n.*260_*261insCAAGTTT
XM_011528654.2:c.*260_*261insCAAGTTT XP_011526956.1:n.*260_*261insCAAGTTT
XR_936511.2:n.2611_2612insCAAGTTT
NM_001207055.2:c.*260_*261insCAAGTTT NP_001193984.1:n.*260_*261insCAAGTTT
NM_001207056.2:c.*260_*261insCAAGTTT NP_001193985.1:n.*260_*261insCAAGTTT
NM_006892.4:c.*260_*261insCAAGTTT MANE Select NP_008823.1:n.*260_*261insCAAGTTT
NM_175848.2:c.*260_*261insCAAGTTT NP_787044.1:n.*260_*261insCAAGTTT
NM_175849.2:c.*260_*261insCAAGTTT NP_787045.1:n.*260_*261insCAAGTTT
NM_175850.3:c.*260_*261insCAAGTTT NP_787046.1:n.*260_*261insCAAGTTT