Canonical Allele Identifier: CA1016994007

Gene: DNMT3B

Linked Data

• gnomAD v3: 20-32805514-A-AT
• gnomAD v4: 20-32805514-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805514_32805515insT , CM000682.2:g.32805514_32805515insT	GRCh38
NC_000020.10:g.31393320_31393321insT , CM000682.1:g.31393320_31393321insT	GRCh37
NC_000020.9:g.30856981_30856982insT	NCBI36
NG_007290.1:g.48130_48131insT , LRG_56:g.48130_48131insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+107_*1252+108insT	ENSP00000512497.1:n.*1252+107_*1252+108insT
ENST00000696232.1:c.2232-2248_2232-2247insT	ENSP00000512498.1:n.2232-2248_2232-2247insT
ENST00000696233.1:c.*975-2248_*975-2247insT	ENSP00000512499.1:n.*975-2248_*975-2247insT
ENST00000696238.1:c.*1044+107_*1044+108insT	ENSP00000512502.1:n.*1044+107_*1044+108insT
ENST00000696239.1:c.2082+107_2082+108insT	ENSP00000512503.1:n.2082+107_2082+108insT
ENST00000696245.1:n.327-695_327-694insT
ENST00000201963.3:c.2277+107_2277+108insT	ENSP00000201963.3:n.2277+107_2277+108insT
ENST00000328111.6:c.2301+107_2301+108insT MANE Select	ENSP00000328547.2:n.2301+107_2301+108insT
ENST00000348286.6:c.2172-2248_2172-2247insT	ENSP00000337764.2:n.2172-2248_2172-2247insT
ENST00000353855.6:c.2241+107_2241+108insT	ENSP00000313397.4:n.2241+107_2241+108insT
ENST00000443239.7:c.2046-2248_2046-2247insT	ENSP00000403169.2:n.2046-2248_2046-2247insT
ENST00000456297.6:c.1944-2248_1944-2247insT	ENSP00000412305.1:n.1944-2248_1944-2247insT
NM_001207055.1:c.2046-2248_2046-2247insT	NP_001193984.1:n.2046-2248_2046-2247insT
NM_001207056.1:c.1944-2248_1944-2247insT	NP_001193985.1:n.1944-2248_1944-2247insT
NM_006892.3:c.2301+107_2301+108insT , LRG_56t1:c.2301+107_2301+108insT	NP_008823.1:n.2301+107_2301+108insT
NM_175848.1:c.2241+107_2241+108insT	NP_787044.1:n.2241+107_2241+108insT
NM_175849.1:c.2172-2248_2172-2247insT	NP_787045.1:n.2172-2248_2172-2247insT
NM_175850.2:c.2277+107_2277+108insT	NP_787046.1:n.2277+107_2277+108insT
XM_011528653.1:c.2208-2248_2208-2247insT	XP_011526955.1:n.2208-2248_2208-2247insT
XM_011528654.1:c.2082-2248_2082-2247insT	XP_011526956.1:n.2082-2248_2082-2247insT
XR_936510.1:n.2268+107_2268+108insT
XR_936511.1:n.2199-2248_2199-2247insT
XR_936512.1:n.2143+107_2143+108insT
XM_011528653.2:c.2208-2248_2208-2247insT	XP_011526955.1:n.2208-2248_2208-2247insT
XM_011528654.2:c.2082-2248_2082-2247insT	XP_011526956.1:n.2082-2248_2082-2247insT
XR_936510.2:n.2279+107_2279+108insT
XR_936511.2:n.2210-2248_2210-2247insT
XR_936512.2:n.2155+107_2155+108insT
NM_001207055.2:c.2046-2248_2046-2247insT	NP_001193984.1:n.2046-2248_2046-2247insT
NM_001207056.2:c.1944-2248_1944-2247insT	NP_001193985.1:n.1944-2248_1944-2247insT
NM_006892.4:c.2301+107_2301+108insT MANE Select	NP_008823.1:n.2301+107_2301+108insT
NM_175848.2:c.2241+107_2241+108insT	NP_787044.1:n.2241+107_2241+108insT
NM_175849.2:c.2172-2248_2172-2247insT	NP_787045.1:n.2172-2248_2172-2247insT
NM_175850.3:c.2277+107_2277+108insT	NP_787046.1:n.2277+107_2277+108insT