Canonical Allele Identifier: CA1016994020

Gene: DNMT3B

Linked Data

• gnomAD v3: 20-32805515-C-CTCG
• gnomAD v4: 20-32805515-C-CTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805516_32805517insCGT , CM000682.2:g.32805516_32805517insCGT	GRCh38
NC_000020.10:g.31393322_31393323insCGT , CM000682.1:g.31393322_31393323insCGT	GRCh37
NC_000020.9:g.30856983_30856984insCGT	NCBI36
NG_007290.1:g.48132_48133insCGT , LRG_56:g.48132_48133insCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+109_*1252+110insCGT	ENSP00000512497.1:n.*1252+109_*1252+110insCGT
ENST00000696232.1:c.2232-2246_2232-2245insCGT	ENSP00000512498.1:n.2232-2246_2232-2245insCGT
ENST00000696233.1:c.*975-2246_*975-2245insCGT	ENSP00000512499.1:n.*975-2246_*975-2245insCGT
ENST00000696238.1:c.*1044+109_*1044+110insCGT	ENSP00000512502.1:n.*1044+109_*1044+110insCGT
ENST00000696239.1:c.2082+109_2082+110insCGT	ENSP00000512503.1:n.2082+109_2082+110insCGT
ENST00000696245.1:n.327-693_327-692insCGT
ENST00000201963.3:c.2277+109_2277+110insCGT	ENSP00000201963.3:n.2277+109_2277+110insCGT
ENST00000328111.6:c.2301+109_2301+110insCGT MANE Select	ENSP00000328547.2:n.2301+109_2301+110insCGT
ENST00000348286.6:c.2172-2246_2172-2245insCGT	ENSP00000337764.2:n.2172-2246_2172-2245insCGT
ENST00000353855.6:c.2241+109_2241+110insCGT	ENSP00000313397.4:n.2241+109_2241+110insCGT
ENST00000443239.7:c.2046-2246_2046-2245insCGT	ENSP00000403169.2:n.2046-2246_2046-2245insCGT
ENST00000456297.6:c.1944-2246_1944-2245insCGT	ENSP00000412305.1:n.1944-2246_1944-2245insCGT
NM_001207055.1:c.2046-2246_2046-2245insCGT	NP_001193984.1:n.2046-2246_2046-2245insCGT
NM_001207056.1:c.1944-2246_1944-2245insCGT	NP_001193985.1:n.1944-2246_1944-2245insCGT
NM_006892.3:c.2301+109_2301+110insCGT , LRG_56t1:c.2301+109_2301+110insCGT	NP_008823.1:n.2301+109_2301+110insCGT
NM_175848.1:c.2241+109_2241+110insCGT	NP_787044.1:n.2241+109_2241+110insCGT
NM_175849.1:c.2172-2246_2172-2245insCGT	NP_787045.1:n.2172-2246_2172-2245insCGT
NM_175850.2:c.2277+109_2277+110insCGT	NP_787046.1:n.2277+109_2277+110insCGT
XM_011528653.1:c.2208-2246_2208-2245insCGT	XP_011526955.1:n.2208-2246_2208-2245insCGT
XM_011528654.1:c.2082-2246_2082-2245insCGT	XP_011526956.1:n.2082-2246_2082-2245insCGT
XR_936510.1:n.2268+109_2268+110insCGT
XR_936511.1:n.2199-2246_2199-2245insCGT
XR_936512.1:n.2143+109_2143+110insCGT
XM_011528653.2:c.2208-2246_2208-2245insCGT	XP_011526955.1:n.2208-2246_2208-2245insCGT
XM_011528654.2:c.2082-2246_2082-2245insCGT	XP_011526956.1:n.2082-2246_2082-2245insCGT
XR_936510.2:n.2279+109_2279+110insCGT
XR_936511.2:n.2210-2246_2210-2245insCGT
XR_936512.2:n.2155+109_2155+110insCGT
NM_001207055.2:c.2046-2246_2046-2245insCGT	NP_001193984.1:n.2046-2246_2046-2245insCGT
NM_001207056.2:c.1944-2246_1944-2245insCGT	NP_001193985.1:n.1944-2246_1944-2245insCGT
NM_006892.4:c.2301+109_2301+110insCGT MANE Select	NP_008823.1:n.2301+109_2301+110insCGT
NM_175848.2:c.2241+109_2241+110insCGT	NP_787044.1:n.2241+109_2241+110insCGT
NM_175849.2:c.2172-2246_2172-2245insCGT	NP_787045.1:n.2172-2246_2172-2245insCGT
NM_175850.3:c.2277+109_2277+110insCGT	NP_787046.1:n.2277+109_2277+110insCGT