Canonical Allele Identifier: CA2741661735

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808195_32808202dup , CM000682.2:g.32808195_32808202dup	GRCh38
NC_000020.10:g.31396001_31396008dup , CM000682.1:g.31396001_31396008dup	GRCh37
NC_000020.9:g.30859662_30859669dup	NCBI36
NG_007290.1:g.50811_50818dup , LRG_56:g.50811_50818dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1805_*1812dup	ENSP00000512497.1:n.*1805_*1812dup
ENST00000696232.1:c.*292_*299dup	ENSP00000512498.1:n.*292_*299dup
ENST00000696233.1:c.*1408_*1415dup	ENSP00000512499.1:n.*1408_*1415dup
ENST00000696238.1:c.*1597_*1604dup	ENSP00000512502.1:n.*1597_*1604dup
ENST00000696245.1:n.879_886dup
ENST00000201963.3:c.*292_*299dup	ENSP00000201963.3:n.*292_*299dup
ENST00000328111.6:c.*292_*299dup MANE Select	ENSP00000328547.2:n.*292_*299dup
ENST00000348286.6:c.*292_*299dup	ENSP00000337764.2:n.*292_*299dup
ENST00000353855.6:c.*292_*299dup	ENSP00000313397.4:n.*292_*299dup
ENST00000443239.7:c.*292_*299dup	ENSP00000403169.2:n.*292_*299dup
NM_001207055.1:c.*292_*299dup	NP_001193984.1:n.*292_*299dup
NM_001207056.1:c.*292_*299dup	NP_001193985.1:n.*292_*299dup
NM_006892.3:c.*292_*299dup , LRG_56t1:c.*292_*299dup	NP_008823.1:n.*292_*299dup
NM_175848.1:c.*292_*299dup	NP_787044.1:n.*292_*299dup
NM_175849.1:c.*292_*299dup	NP_787045.1:n.*292_*299dup
NM_175850.2:c.*292_*299dup	NP_787046.1:n.*292_*299dup
XM_011528653.1:c.*292_*299dup	XP_011526955.1:n.*292_*299dup
XM_011528654.1:c.*292_*299dup	XP_011526956.1:n.*292_*299dup
XR_936511.1:n.2632_2639dup
XM_011528653.2:c.*292_*299dup	XP_011526955.1:n.*292_*299dup
XM_011528654.2:c.*292_*299dup	XP_011526956.1:n.*292_*299dup
XR_936511.2:n.2643_2650dup
NM_001207055.2:c.*292_*299dup	NP_001193984.1:n.*292_*299dup
NM_001207056.2:c.*292_*299dup	NP_001193985.1:n.*292_*299dup
NM_006892.4:c.*292_*299dup MANE Select	NP_008823.1:n.*292_*299dup
NM_175848.2:c.*292_*299dup	NP_787044.1:n.*292_*299dup
NM_175849.2:c.*292_*299dup	NP_787045.1:n.*292_*299dup
NM_175850.3:c.*292_*299dup	NP_787046.1:n.*292_*299dup