Canonical Allele Identifier: CA2652423157
Gene: DNMT3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32805258_32805259insCCCCC , CM000682.2:g.32805258_32805259insCCCCC GRCh38
NC_000020.10:g.31393064_31393065insCCCCC , CM000682.1:g.31393064_31393065insCCCCC GRCh37
NC_000020.9:g.30856725_30856726insCCCCC NCBI36
NG_007290.1:g.47874_47875insCCCCC , LRG_56:g.47874_47875insCCCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000696231.1:c.*1183-80_*1183-79insCCCCC ENSP00000512497.1:n.*1183-80_*1183-79insC...
ENST00000696232.1:c.2232-2504_2232-2503insCCCCC ENSP00000512498.1:n.2232-2504_2232-2503in...
ENST00000696233.1:c.*975-2504_*975-2503insCCCCC ENSP00000512499.1:n.*975-2504_*975-2503in...
ENST00000696238.1:c.*975-80_*975-79insCCCCC ENSP00000512502.1:n.*975-80_*975-79insCCC...
ENST00000696239.1:c.2013-80_2013-79insCCCCC ENSP00000512503.1:n.2013-80_2013-79insCCC...
ENST00000696245.1:n.327-951_327-950insCCCCC
ENST00000201963.3:c.2208-80_2208-79insCCCCC ENSP00000201963.3:n.2208-80_2208-79insCCC...
ENST00000328111.6:c.2232-80_2232-79insCCCCC MANE Select ENSP00000328547.2:n.2232-80_2232-79insCCC...
ENST00000348286.6:c.2172-2504_2172-2503insCCCCC ENSP00000337764.2:n.2172-2504_2172-2503in...
ENST00000353855.6:c.2172-80_2172-79insCCCCC ENSP00000313397.4:n.2172-80_2172-79insCCC...
ENST00000443239.7:c.2046-2504_2046-2503insCCCCC ENSP00000403169.2:n.2046-2504_2046-2503in...
ENST00000456297.6:c.1944-2504_1944-2503insCCCCC ENSP00000412305.1:n.1944-2504_1944-2503in...
NM_001207055.1:c.2046-2504_2046-2503insCCCCC NP_001193984.1:n.2046-2504_2046-2503insCC...
NM_001207056.1:c.1944-2504_1944-2503insCCCCC NP_001193985.1:n.1944-2504_1944-2503insCC...
NM_006892.3:c.2232-80_2232-79insCCCCC , LRG_56t1:c.2232-80_2232-79insCCCCC NP_008823.1:n.2232-80_2232-79insCCCCC
NM_175848.1:c.2172-80_2172-79insCCCCC NP_787044.1:n.2172-80_2172-79insCCCCC
NM_175849.1:c.2172-2504_2172-2503insCCCCC NP_787045.1:n.2172-2504_2172-2503insCCCCC...
NM_175850.2:c.2208-80_2208-79insCCCCC NP_787046.1:n.2208-80_2208-79insCCCCC
XM_011528653.1:c.2208-2504_2208-2503insCCCCC XP_011526955.1:n.2208-2504_2208-2503insCC...
XM_011528654.1:c.2082-2504_2082-2503insCCCCC XP_011526956.1:n.2082-2504_2082-2503insCC...
XR_936510.1:n.2199-80_2199-79insCCCCC
XR_936511.1:n.2199-2504_2199-2503insCCCCC
XR_936512.1:n.2074-80_2074-79insCCCCC
XM_011528653.2:c.2208-2504_2208-2503insCCCCC XP_011526955.1:n.2208-2504_2208-2503insCC...
XM_011528654.2:c.2082-2504_2082-2503insCCCCC XP_011526956.1:n.2082-2504_2082-2503insCC...
XR_936510.2:n.2210-80_2210-79insCCCCC
XR_936511.2:n.2210-2504_2210-2503insCCCCC
XR_936512.2:n.2086-80_2086-79insCCCCC
NM_001207055.2:c.2046-2504_2046-2503insCCCCC NP_001193984.1:n.2046-2504_2046-2503insCC...
NM_001207056.2:c.1944-2504_1944-2503insCCCCC NP_001193985.1:n.1944-2504_1944-2503insCC...
NM_006892.4:c.2232-80_2232-79insCCCCC MANE Select NP_008823.1:n.2232-80_2232-79insCCCCC
NM_175848.2:c.2172-80_2172-79insCCCCC NP_787044.1:n.2172-80_2172-79insCCCCC
NM_175849.2:c.2172-2504_2172-2503insCCCCC NP_787045.1:n.2172-2504_2172-2503insCCCCC...
NM_175850.3:c.2208-80_2208-79insCCCCC NP_787046.1:n.2208-80_2208-79insCCCCC