Canonical Allele Identifier: CA743667246

Gene: DNMT3B

Linked Data

• dbSNP Id: rs1446038380
• MyVariant Identifiers: chr20:g.31393371_31393376del (hg19) ; chr20:g.32805565_32805570del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805567_32805572del , CM000682.2:g.32805567_32805572del	GRCh38
NC_000020.10:g.31393373_31393378del , CM000682.1:g.31393373_31393378del	GRCh37
NC_000020.9:g.30857034_30857039del	NCBI36
NG_007290.1:g.48183_48188del , LRG_56:g.48183_48188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+160_*1252+165del	ENSP00000512497.1:n.*1252+160_*1252+165del
ENST00000696232.1:c.2232-2195_2232-2190del	ENSP00000512498.1:n.2232-2195_2232-2190del
ENST00000696233.1:c.*975-2195_*975-2190del	ENSP00000512499.1:n.*975-2195_*975-2190del
ENST00000696238.1:c.*1044+160_*1044+165del	ENSP00000512502.1:n.*1044+160_*1044+165del
ENST00000696239.1:c.2082+160_2082+165del	ENSP00000512503.1:n.2082+160_2082+165del
ENST00000696245.1:n.327-642_327-637del
ENST00000201963.3:c.2277+160_2277+165del	ENSP00000201963.3:n.2277+160_2277+165del
ENST00000328111.6:c.2301+160_2301+165del MANE Select	ENSP00000328547.2:n.2301+160_2301+165del
ENST00000348286.6:c.2172-2195_2172-2190del	ENSP00000337764.2:n.2172-2195_2172-2190del
ENST00000353855.6:c.2241+160_2241+165del	ENSP00000313397.4:n.2241+160_2241+165del
ENST00000443239.7:c.2046-2195_2046-2190del	ENSP00000403169.2:n.2046-2195_2046-2190del
ENST00000456297.6:c.1944-2195_1944-2190del	ENSP00000412305.1:n.1944-2195_1944-2190del
NM_001207055.1:c.2046-2195_2046-2190del	NP_001193984.1:n.2046-2195_2046-2190del
NM_001207056.1:c.1944-2195_1944-2190del	NP_001193985.1:n.1944-2195_1944-2190del
NM_006892.3:c.2301+160_2301+165del , LRG_56t1:c.2301+160_2301+165del	NP_008823.1:n.2301+160_2301+165del
NM_175848.1:c.2241+160_2241+165del	NP_787044.1:n.2241+160_2241+165del
NM_175849.1:c.2172-2195_2172-2190del	NP_787045.1:n.2172-2195_2172-2190del
NM_175850.2:c.2277+160_2277+165del	NP_787046.1:n.2277+160_2277+165del
XM_011528653.1:c.2208-2195_2208-2190del	XP_011526955.1:n.2208-2195_2208-2190del
XM_011528654.1:c.2082-2195_2082-2190del	XP_011526956.1:n.2082-2195_2082-2190del
XR_936510.1:n.2268+160_2268+165del
XR_936511.1:n.2199-2195_2199-2190del
XR_936512.1:n.2143+160_2143+165del
XM_011528653.2:c.2208-2195_2208-2190del	XP_011526955.1:n.2208-2195_2208-2190del
XM_011528654.2:c.2082-2195_2082-2190del	XP_011526956.1:n.2082-2195_2082-2190del
XR_936510.2:n.2279+160_2279+165del
XR_936511.2:n.2210-2195_2210-2190del
XR_936512.2:n.2155+160_2155+165del
NM_001207055.2:c.2046-2195_2046-2190del	NP_001193984.1:n.2046-2195_2046-2190del
NM_001207056.2:c.1944-2195_1944-2190del	NP_001193985.1:n.1944-2195_1944-2190del
NM_006892.4:c.2301+160_2301+165del MANE Select	NP_008823.1:n.2301+160_2301+165del
NM_175848.2:c.2241+160_2241+165del	NP_787044.1:n.2241+160_2241+165del
NM_175849.2:c.2172-2195_2172-2190del	NP_787045.1:n.2172-2195_2172-2190del
NM_175850.3:c.2277+160_2277+165del	NP_787046.1:n.2277+160_2277+165del