Canonical Allele Identifier: CA2652423195
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805457_32805458insCCCCACTTGGA , CM000682.2:g.32805457_32805458insCCCCACTTGGA GRCh38
NC_000020.10:g.31393263_31393264insCCCCACTTGGA , CM000682.1:g.31393263_31393264insCCCCACTTGGA GRCh37
NC_000020.9:g.30856924_30856925insCCCCACTTGGA NCBI36
NG_007290.1:g.48073_48074insCCCCACTTGGA , LRG_56:g.48073_48074insCCCCACTTGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1252+50_*1252+51insCCCCACTTGGA ENSP00000512497.1:n.*1252+50_*1252+51insCCCCACTTGGA
ENST00000696232.1:c.2232-2305_2232-2304insCCCCACTTGGA ENSP00000512498.1:n.2232-2305_2232-2304insCCCCACTTGGA
ENST00000696233.1:c.*975-2305_*975-2304insCCCCACTTGGA ENSP00000512499.1:n.*975-2305_*975-2304insCCCCACTTGGA
ENST00000696238.1:c.*1044+50_*1044+51insCCCCACTTGGA ENSP00000512502.1:n.*1044+50_*1044+51insCCCCACTTGGA
ENST00000696239.1:c.2082+50_2082+51insCCCCACTTGGA ENSP00000512503.1:n.2082+50_2082+51insCCCCACTTGGA
ENST00000696245.1:n.327-752_327-751insCCCCACTTGGA
ENST00000201963.3:c.2277+50_2277+51insCCCCACTTGGA ENSP00000201963.3:n.2277+50_2277+51insCCCCACTTGGA
ENST00000328111.6:c.2301+50_2301+51insCCCCACTTGGA MANE Select ENSP00000328547.2:n.2301+50_2301+51insCCCCACTTGGA
ENST00000348286.6:c.2172-2305_2172-2304insCCCCACTTGGA ENSP00000337764.2:n.2172-2305_2172-2304insCCCCACTTGGA
ENST00000353855.6:c.2241+50_2241+51insCCCCACTTGGA ENSP00000313397.4:n.2241+50_2241+51insCCCCACTTGGA
ENST00000443239.7:c.2046-2305_2046-2304insCCCCACTTGGA ENSP00000403169.2:n.2046-2305_2046-2304insCCCCACTTGGA
ENST00000456297.6:c.1944-2305_1944-2304insCCCCACTTGGA ENSP00000412305.1:n.1944-2305_1944-2304insCCCCACTTGGA
NM_001207055.1:c.2046-2305_2046-2304insCCCCACTTGGA NP_001193984.1:n.2046-2305_2046-2304insCCCCACTTGGA
NM_001207056.1:c.1944-2305_1944-2304insCCCCACTTGGA NP_001193985.1:n.1944-2305_1944-2304insCCCCACTTGGA
NM_006892.3:c.2301+50_2301+51insCCCCACTTGGA , LRG_56t1:c.2301+50_2301+51insCCCCACTTGGA NP_008823.1:n.2301+50_2301+51insCCCCACTTGGA
NM_175848.1:c.2241+50_2241+51insCCCCACTTGGA NP_787044.1:n.2241+50_2241+51insCCCCACTTGGA
NM_175849.1:c.2172-2305_2172-2304insCCCCACTTGGA NP_787045.1:n.2172-2305_2172-2304insCCCCACTTGGA
NM_175850.2:c.2277+50_2277+51insCCCCACTTGGA NP_787046.1:n.2277+50_2277+51insCCCCACTTGGA
XM_011528653.1:c.2208-2305_2208-2304insCCCCACTTGGA XP_011526955.1:n.2208-2305_2208-2304insCCCCACTTGGA
XM_011528654.1:c.2082-2305_2082-2304insCCCCACTTGGA XP_011526956.1:n.2082-2305_2082-2304insCCCCACTTGGA
XR_936510.1:n.2268+50_2268+51insCCCCACTTGGA
XR_936511.1:n.2199-2305_2199-2304insCCCCACTTGGA
XR_936512.1:n.2143+50_2143+51insCCCCACTTGGA
XM_011528653.2:c.2208-2305_2208-2304insCCCCACTTGGA XP_011526955.1:n.2208-2305_2208-2304insCCCCACTTGGA
XM_011528654.2:c.2082-2305_2082-2304insCCCCACTTGGA XP_011526956.1:n.2082-2305_2082-2304insCCCCACTTGGA
XR_936510.2:n.2279+50_2279+51insCCCCACTTGGA
XR_936511.2:n.2210-2305_2210-2304insCCCCACTTGGA
XR_936512.2:n.2155+50_2155+51insCCCCACTTGGA
NM_001207055.2:c.2046-2305_2046-2304insCCCCACTTGGA NP_001193984.1:n.2046-2305_2046-2304insCCCCACTTGGA
NM_001207056.2:c.1944-2305_1944-2304insCCCCACTTGGA NP_001193985.1:n.1944-2305_1944-2304insCCCCACTTGGA
NM_006892.4:c.2301+50_2301+51insCCCCACTTGGA MANE Select NP_008823.1:n.2301+50_2301+51insCCCCACTTGGA
NM_175848.2:c.2241+50_2241+51insCCCCACTTGGA NP_787044.1:n.2241+50_2241+51insCCCCACTTGGA
NM_175849.2:c.2172-2305_2172-2304insCCCCACTTGGA NP_787045.1:n.2172-2305_2172-2304insCCCCACTTGGA
NM_175850.3:c.2277+50_2277+51insCCCCACTTGGA NP_787046.1:n.2277+50_2277+51insCCCCACTTGGA