Canonical Allele Identifier: CA2816162907

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787580_32787581del , CM000682.2:g.32787580_32787581del	GRCh38
NC_000020.10:g.31375386_31375387del , CM000682.1:g.31375386_31375387del	GRCh37
NC_000020.9:g.30839047_30839048del	NCBI36
NG_007290.1:g.30196_30197del , LRG_56:g.30196_30197del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.654+129_654+130del	ENSP00000512497.1:n.654+129_654+130del
ENST00000696232.1:c.654+129_654+130del	ENSP00000512498.1:n.654+129_654+130del
ENST00000696233.1:c.654+129_654+130del	ENSP00000512499.1:n.654+129_654+130del
ENST00000696234.1:n.638+129_638+130del
ENST00000696235.1:c.528+129_528+130del	ENSP00000512500.1:n.528+129_528+130del
ENST00000696236.1:c.528+129_528+130del	ENSP00000512501.1:n.528+129_528+130del
ENST00000696238.1:c.654+129_654+130del	ENSP00000512502.1:n.654+129_654+130del
ENST00000696239.1:c.654+129_654+130del	ENSP00000512503.1:n.654+129_654+130del
ENST00000201963.3:c.690+129_690+130del	ENSP00000201963.3:n.690+129_690+130del
ENST00000328111.6:c.654+129_654+130del MANE Select	ENSP00000328547.2:n.654+129_654+130del
ENST00000348286.6:c.654+129_654+130del	ENSP00000337764.2:n.654+129_654+130del
ENST00000353855.6:c.654+129_654+130del	ENSP00000313397.4:n.654+129_654+130del
ENST00000443239.7:c.528+129_528+130del	ENSP00000403169.2:n.528+129_528+130del
ENST00000456297.6:c.426+129_426+130del	ENSP00000412305.1:n.426+129_426+130del
NM_001207055.1:c.528+129_528+130del	NP_001193984.1:n.528+129_528+130del
NM_001207056.1:c.426+129_426+130del	NP_001193985.1:n.426+129_426+130del
NM_006892.3:c.654+129_654+130del , LRG_56t1:c.654+129_654+130del	NP_008823.1:n.654+129_654+130del
NM_175848.1:c.654+129_654+130del	NP_787044.1:n.654+129_654+130del
NM_175849.1:c.654+129_654+130del	NP_787045.1:n.654+129_654+130del
NM_175850.2:c.690+129_690+130del	NP_787046.1:n.690+129_690+130del
XM_011528653.1:c.690+129_690+130del	XP_011526955.1:n.690+129_690+130del
XM_011528654.1:c.564+129_564+130del	XP_011526956.1:n.564+129_564+130del
XR_936510.1:n.826+129_826+130del
XR_936511.1:n.826+129_826+130del
XR_936512.1:n.701+129_701+130del
XM_011528653.2:c.690+129_690+130del	XP_011526955.1:n.690+129_690+130del
XM_011528654.2:c.564+129_564+130del	XP_011526956.1:n.564+129_564+130del
XR_936510.2:n.837+129_837+130del
XR_936511.2:n.837+129_837+130del
XR_936512.2:n.713+129_713+130del
NM_001207055.2:c.528+129_528+130del	NP_001193984.1:n.528+129_528+130del
NM_001207056.2:c.426+129_426+130del	NP_001193985.1:n.426+129_426+130del
NM_006892.4:c.654+129_654+130del MANE Select	NP_008823.1:n.654+129_654+130del
NM_175848.2:c.654+129_654+130del	NP_787044.1:n.654+129_654+130del
NM_175849.2:c.654+129_654+130del	NP_787045.1:n.654+129_654+130del
NM_175850.3:c.690+129_690+130del	NP_787046.1:n.690+129_690+130del