Canonical Allele Identifier: CA2739277113

Gene: DNMT3B

Linked Data

• ClinVar Variation Id: 2817106
• ClinVar RCV Id: RCV003760923

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805414_32805415insACT , CM000682.2:g.32805414_32805415insACT	GRCh38
NC_000020.10:g.31393220_31393221insACT , CM000682.1:g.31393220_31393221insACT	GRCh37
NC_000020.9:g.30856881_30856882insACT	NCBI36
NG_007290.1:g.48030_48031insACT , LRG_56:g.48030_48031insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+7_*1252+8insACT	ENSP00000512497.1:n.*1252+7_*1252+8insACT
ENST00000696232.1:c.2232-2348_2232-2347insACT	ENSP00000512498.1:n.2232-2348_2232-2347insACT
ENST00000696233.1:c.*975-2348_*975-2347insACT	ENSP00000512499.1:n.*975-2348_*975-2347insACT
ENST00000696238.1:c.*1044+7_*1044+8insACT	ENSP00000512502.1:n.*1044+7_*1044+8insACT
ENST00000696239.1:c.2082+7_2082+8insACT	ENSP00000512503.1:n.2082+7_2082+8insACT
ENST00000696245.1:n.327-795_327-794insACT
ENST00000201963.3:c.2277+7_2277+8insACT	ENSP00000201963.3:n.2277+7_2277+8insACT
ENST00000328111.6:c.2301+7_2301+8insACT MANE Select	ENSP00000328547.2:n.2301+7_2301+8insACT
ENST00000348286.6:c.2172-2348_2172-2347insACT	ENSP00000337764.2:n.2172-2348_2172-2347insACT
ENST00000353855.6:c.2241+7_2241+8insACT	ENSP00000313397.4:n.2241+7_2241+8insACT
ENST00000443239.7:c.2046-2348_2046-2347insACT	ENSP00000403169.2:n.2046-2348_2046-2347insACT
ENST00000456297.6:c.1944-2348_1944-2347insACT	ENSP00000412305.1:n.1944-2348_1944-2347insACT
NM_001207055.1:c.2046-2348_2046-2347insACT	NP_001193984.1:n.2046-2348_2046-2347insACT
NM_001207056.1:c.1944-2348_1944-2347insACT	NP_001193985.1:n.1944-2348_1944-2347insACT
NM_006892.3:c.2301+7_2301+8insACT , LRG_56t1:c.2301+7_2301+8insACT	NP_008823.1:n.2301+7_2301+8insACT
NM_175848.1:c.2241+7_2241+8insACT	NP_787044.1:n.2241+7_2241+8insACT
NM_175849.1:c.2172-2348_2172-2347insACT	NP_787045.1:n.2172-2348_2172-2347insACT
NM_175850.2:c.2277+7_2277+8insACT	NP_787046.1:n.2277+7_2277+8insACT
XM_011528653.1:c.2208-2348_2208-2347insACT	XP_011526955.1:n.2208-2348_2208-2347insACT
XM_011528654.1:c.2082-2348_2082-2347insACT	XP_011526956.1:n.2082-2348_2082-2347insACT
XR_936510.1:n.2268+7_2268+8insACT
XR_936511.1:n.2199-2348_2199-2347insACT
XR_936512.1:n.2143+7_2143+8insACT
XM_011528653.2:c.2208-2348_2208-2347insACT	XP_011526955.1:n.2208-2348_2208-2347insACT
XM_011528654.2:c.2082-2348_2082-2347insACT	XP_011526956.1:n.2082-2348_2082-2347insACT
XR_936510.2:n.2279+7_2279+8insACT
XR_936511.2:n.2210-2348_2210-2347insACT
XR_936512.2:n.2155+7_2155+8insACT
NM_001207055.2:c.2046-2348_2046-2347insACT	NP_001193984.1:n.2046-2348_2046-2347insACT
NM_001207056.2:c.1944-2348_1944-2347insACT	NP_001193985.1:n.1944-2348_1944-2347insACT
NM_006892.4:c.2301+7_2301+8insACT MANE Select	NP_008823.1:n.2301+7_2301+8insACT
NM_175848.2:c.2241+7_2241+8insACT	NP_787044.1:n.2241+7_2241+8insACT
NM_175849.2:c.2172-2348_2172-2347insACT	NP_787045.1:n.2172-2348_2172-2347insACT
NM_175850.3:c.2277+7_2277+8insACT	NP_787046.1:n.2277+7_2277+8insACT