Canonical Allele Identifier: CA2652423213

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32805506-CCCACGTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805508_32805515del , CM000682.2:g.32805508_32805515del	GRCh38
NC_000020.10:g.31393314_31393321del , CM000682.1:g.31393314_31393321del	GRCh37
NC_000020.9:g.30856975_30856982del	NCBI36
NG_007290.1:g.48124_48131del , LRG_56:g.48124_48131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+101_*1252+108del	ENSP00000512497.1:n.*1252+101_*1252+108del
ENST00000696232.1:c.2232-2254_2232-2247del	ENSP00000512498.1:n.2232-2254_2232-2247del
ENST00000696233.1:c.*975-2254_*975-2247del	ENSP00000512499.1:n.*975-2254_*975-2247del
ENST00000696238.1:c.*1044+101_*1044+108del	ENSP00000512502.1:n.*1044+101_*1044+108del
ENST00000696239.1:c.2082+101_2082+108del	ENSP00000512503.1:n.2082+101_2082+108del
ENST00000696245.1:n.327-701_327-694del
ENST00000201963.3:c.2277+101_2277+108del	ENSP00000201963.3:n.2277+101_2277+108del
ENST00000328111.6:c.2301+101_2301+108del MANE Select	ENSP00000328547.2:n.2301+101_2301+108del
ENST00000348286.6:c.2172-2254_2172-2247del	ENSP00000337764.2:n.2172-2254_2172-2247del
ENST00000353855.6:c.2241+101_2241+108del	ENSP00000313397.4:n.2241+101_2241+108del
ENST00000443239.7:c.2046-2254_2046-2247del	ENSP00000403169.2:n.2046-2254_2046-2247del
ENST00000456297.6:c.1944-2254_1944-2247del	ENSP00000412305.1:n.1944-2254_1944-2247del
NM_001207055.1:c.2046-2254_2046-2247del	NP_001193984.1:n.2046-2254_2046-2247del
NM_001207056.1:c.1944-2254_1944-2247del	NP_001193985.1:n.1944-2254_1944-2247del
NM_006892.3:c.2301+101_2301+108del , LRG_56t1:c.2301+101_2301+108del	NP_008823.1:n.2301+101_2301+108del
NM_175848.1:c.2241+101_2241+108del	NP_787044.1:n.2241+101_2241+108del
NM_175849.1:c.2172-2254_2172-2247del	NP_787045.1:n.2172-2254_2172-2247del
NM_175850.2:c.2277+101_2277+108del	NP_787046.1:n.2277+101_2277+108del
XM_011528653.1:c.2208-2254_2208-2247del	XP_011526955.1:n.2208-2254_2208-2247del
XM_011528654.1:c.2082-2254_2082-2247del	XP_011526956.1:n.2082-2254_2082-2247del
XR_936510.1:n.2268+101_2268+108del
XR_936511.1:n.2199-2254_2199-2247del
XR_936512.1:n.2143+101_2143+108del
XM_011528653.2:c.2208-2254_2208-2247del	XP_011526955.1:n.2208-2254_2208-2247del
XM_011528654.2:c.2082-2254_2082-2247del	XP_011526956.1:n.2082-2254_2082-2247del
XR_936510.2:n.2279+101_2279+108del
XR_936511.2:n.2210-2254_2210-2247del
XR_936512.2:n.2155+101_2155+108del
NM_001207055.2:c.2046-2254_2046-2247del	NP_001193984.1:n.2046-2254_2046-2247del
NM_001207056.2:c.1944-2254_1944-2247del	NP_001193985.1:n.1944-2254_1944-2247del
NM_006892.4:c.2301+101_2301+108del MANE Select	NP_008823.1:n.2301+101_2301+108del
NM_175848.2:c.2241+101_2241+108del	NP_787044.1:n.2241+101_2241+108del
NM_175849.2:c.2172-2254_2172-2247del	NP_787045.1:n.2172-2254_2172-2247del
NM_175850.3:c.2277+101_2277+108del	NP_787046.1:n.2277+101_2277+108del