Canonical Allele Identifier: CA2509052722

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805149_32805150insAGAAACC , CM000682.2:g.32805149_32805150insAGAAACC	GRCh38
NC_000020.10:g.31392955_31392956insAGAAACC , CM000682.1:g.31392955_31392956insAGAAACC	GRCh37
NC_000020.9:g.30856616_30856617insAGAAACC	NCBI36
NG_007290.1:g.47765_47766insAGAAACC , LRG_56:g.47765_47766insAGAAACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1183-189_*1183-188insAGAAACC	ENSP00000512497.1:n.*1183-189_*1183-188insAGAAACC
ENST00000696232.1:c.2232-2613_2232-2612insAGAAACC	ENSP00000512498.1:n.2232-2613_2232-2612insAGAAACC
ENST00000696233.1:c.*975-2613_*975-2612insAGAAACC	ENSP00000512499.1:n.*975-2613_*975-2612insAGAAACC
ENST00000696238.1:c.*975-189_*975-188insAGAAACC	ENSP00000512502.1:n.*975-189_*975-188insAGAAACC
ENST00000696239.1:c.2013-189_2013-188insAGAAACC	ENSP00000512503.1:n.2013-189_2013-188insAGAAACC
ENST00000696245.1:n.327-1060_327-1059insAGAAACC
ENST00000201963.3:c.2208-189_2208-188insAGAAACC	ENSP00000201963.3:n.2208-189_2208-188insAGAAACC
ENST00000328111.6:c.2232-189_2232-188insAGAAACC MANE Select	ENSP00000328547.2:n.2232-189_2232-188insAGAAACC
ENST00000348286.6:c.2172-2613_2172-2612insAGAAACC	ENSP00000337764.2:n.2172-2613_2172-2612insAGAAACC
ENST00000353855.6:c.2172-189_2172-188insAGAAACC	ENSP00000313397.4:n.2172-189_2172-188insAGAAACC
ENST00000443239.7:c.2046-2613_2046-2612insAGAAACC	ENSP00000403169.2:n.2046-2613_2046-2612insAGAAACC
ENST00000456297.6:c.1944-2613_1944-2612insAGAAACC	ENSP00000412305.1:n.1944-2613_1944-2612insAGAAACC
NM_001207055.1:c.2046-2613_2046-2612insAGAAACC	NP_001193984.1:n.2046-2613_2046-2612insAGAAACC
NM_001207056.1:c.1944-2613_1944-2612insAGAAACC	NP_001193985.1:n.1944-2613_1944-2612insAGAAACC
NM_006892.3:c.2232-189_2232-188insAGAAACC , LRG_56t1:c.2232-189_2232-188insAGAAACC	NP_008823.1:n.2232-189_2232-188insAGAAACC
NM_175848.1:c.2172-189_2172-188insAGAAACC	NP_787044.1:n.2172-189_2172-188insAGAAACC
NM_175849.1:c.2172-2613_2172-2612insAGAAACC	NP_787045.1:n.2172-2613_2172-2612insAGAAACC
NM_175850.2:c.2208-189_2208-188insAGAAACC	NP_787046.1:n.2208-189_2208-188insAGAAACC
XM_011528653.1:c.2208-2613_2208-2612insAGAAACC	XP_011526955.1:n.2208-2613_2208-2612insAGAAACC
XM_011528654.1:c.2082-2613_2082-2612insAGAAACC	XP_011526956.1:n.2082-2613_2082-2612insAGAAACC
XR_936510.1:n.2199-189_2199-188insAGAAACC
XR_936511.1:n.2199-2613_2199-2612insAGAAACC
XR_936512.1:n.2074-189_2074-188insAGAAACC
XM_011528653.2:c.2208-2613_2208-2612insAGAAACC	XP_011526955.1:n.2208-2613_2208-2612insAGAAACC
XM_011528654.2:c.2082-2613_2082-2612insAGAAACC	XP_011526956.1:n.2082-2613_2082-2612insAGAAACC
XR_936510.2:n.2210-189_2210-188insAGAAACC
XR_936511.2:n.2210-2613_2210-2612insAGAAACC
XR_936512.2:n.2086-189_2086-188insAGAAACC
NM_001207055.2:c.2046-2613_2046-2612insAGAAACC	NP_001193984.1:n.2046-2613_2046-2612insAGAAACC
NM_001207056.2:c.1944-2613_1944-2612insAGAAACC	NP_001193985.1:n.1944-2613_1944-2612insAGAAACC
NM_006892.4:c.2232-189_2232-188insAGAAACC MANE Select	NP_008823.1:n.2232-189_2232-188insAGAAACC
NM_175848.2:c.2172-189_2172-188insAGAAACC	NP_787044.1:n.2172-189_2172-188insAGAAACC
NM_175849.2:c.2172-2613_2172-2612insAGAAACC	NP_787045.1:n.2172-2613_2172-2612insAGAAACC
NM_175850.3:c.2208-189_2208-188insAGAAACC	NP_787046.1:n.2208-189_2208-188insAGAAACC