Canonical Allele Identifier: CA2652423182

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32805416-AGCTGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805419_32805424del , CM000682.2:g.32805419_32805424del	GRCh38
NC_000020.10:g.31393225_31393230del , CM000682.1:g.31393225_31393230del	GRCh37
NC_000020.9:g.30856886_30856891del	NCBI36
NG_007290.1:g.48035_48040del , LRG_56:g.48035_48040del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+12_*1252+17del	ENSP00000512497.1:n.*1252+12_*1252+17del
ENST00000696232.1:c.2232-2343_2232-2338del	ENSP00000512498.1:n.2232-2343_2232-2338del
ENST00000696233.1:c.*975-2343_*975-2338del	ENSP00000512499.1:n.*975-2343_*975-2338del
ENST00000696238.1:c.*1044+12_*1044+17del	ENSP00000512502.1:n.*1044+12_*1044+17del
ENST00000696239.1:c.2082+12_2082+17del	ENSP00000512503.1:n.2082+12_2082+17del
ENST00000696245.1:n.327-790_327-785del
ENST00000201963.3:c.2277+12_2277+17del	ENSP00000201963.3:n.2277+12_2277+17del
ENST00000328111.6:c.2301+12_2301+17del MANE Select	ENSP00000328547.2:n.2301+12_2301+17del
ENST00000348286.6:c.2172-2343_2172-2338del	ENSP00000337764.2:n.2172-2343_2172-2338del
ENST00000353855.6:c.2241+12_2241+17del	ENSP00000313397.4:n.2241+12_2241+17del
ENST00000443239.7:c.2046-2343_2046-2338del	ENSP00000403169.2:n.2046-2343_2046-2338del
ENST00000456297.6:c.1944-2343_1944-2338del	ENSP00000412305.1:n.1944-2343_1944-2338del
NM_001207055.1:c.2046-2343_2046-2338del	NP_001193984.1:n.2046-2343_2046-2338del
NM_001207056.1:c.1944-2343_1944-2338del	NP_001193985.1:n.1944-2343_1944-2338del
NM_006892.3:c.2301+12_2301+17del , LRG_56t1:c.2301+12_2301+17del	NP_008823.1:n.2301+12_2301+17del
NM_175848.1:c.2241+12_2241+17del	NP_787044.1:n.2241+12_2241+17del
NM_175849.1:c.2172-2343_2172-2338del	NP_787045.1:n.2172-2343_2172-2338del
NM_175850.2:c.2277+12_2277+17del	NP_787046.1:n.2277+12_2277+17del
XM_011528653.1:c.2208-2343_2208-2338del	XP_011526955.1:n.2208-2343_2208-2338del
XM_011528654.1:c.2082-2343_2082-2338del	XP_011526956.1:n.2082-2343_2082-2338del
XR_936510.1:n.2268+12_2268+17del
XR_936511.1:n.2199-2343_2199-2338del
XR_936512.1:n.2143+12_2143+17del
XM_011528653.2:c.2208-2343_2208-2338del	XP_011526955.1:n.2208-2343_2208-2338del
XM_011528654.2:c.2082-2343_2082-2338del	XP_011526956.1:n.2082-2343_2082-2338del
XR_936510.2:n.2279+12_2279+17del
XR_936511.2:n.2210-2343_2210-2338del
XR_936512.2:n.2155+12_2155+17del
NM_001207055.2:c.2046-2343_2046-2338del	NP_001193984.1:n.2046-2343_2046-2338del
NM_001207056.2:c.1944-2343_1944-2338del	NP_001193985.1:n.1944-2343_1944-2338del
NM_006892.4:c.2301+12_2301+17del MANE Select	NP_008823.1:n.2301+12_2301+17del
NM_175848.2:c.2241+12_2241+17del	NP_787044.1:n.2241+12_2241+17del
NM_175849.2:c.2172-2343_2172-2338del	NP_787045.1:n.2172-2343_2172-2338del
NM_175850.3:c.2277+12_2277+17del	NP_787046.1:n.2277+12_2277+17del