Canonical Allele Identifier: CA2360466354

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808155_32808163delinsCTAAAACTT , CM000682.2:g.32808155_32808163delinsCTAAAACTT	GRCh38
NC_000020.10:g.31395961_31395969delinsCTAAAACTT , CM000682.1:g.31395961_31395969delinsCTAAAACTT	GRCh37
NC_000020.9:g.30859622_30859630delinsCTAAAACTT	NCBI36
NG_007290.1:g.50771_50779delinsCTAAAACTT , LRG_56:g.50771_50779delinsCTAAAACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1765_*1773delinsCTAAAACTT	ENSP00000512497.1:n.*1765_*1773delinsCTAAAACTT
ENST00000696232.1:c.*252_*260delinsCTAAAACTT	ENSP00000512498.1:n.*252_*260delinsCTAAAACTT
ENST00000696233.1:c.*1368_*1376delinsCTAAAACTT	ENSP00000512499.1:n.*1368_*1376delinsCTAAAACTT
ENST00000696238.1:c.*1557_*1565delinsCTAAAACTT	ENSP00000512502.1:n.*1557_*1565delinsCTAAAACTT
ENST00000696245.1:n.839_847delinsCTAAAACTT
ENST00000201963.3:c.*252_*260delinsCTAAAACTT	ENSP00000201963.3:n.*252_*260delinsCTAAAACTT
ENST00000328111.6:c.*252_*260delinsCTAAAACTT MANE Select	ENSP00000328547.2:n.*252_*260delinsCTAAAACTT
ENST00000348286.6:c.*252_*260delinsCTAAAACTT	ENSP00000337764.2:n.*252_*260delinsCTAAAACTT
ENST00000353855.6:c.*252_*260delinsCTAAAACTT	ENSP00000313397.4:n.*252_*260delinsCTAAAACTT
ENST00000443239.7:c.*252_*260delinsCTAAAACTT	ENSP00000403169.2:n.*252_*260delinsCTAAAACTT
NM_001207055.1:c.*252_*260delinsCTAAAACTT	NP_001193984.1:n.*252_*260delinsCTAAAACTT
NM_001207056.1:c.*252_*260delinsCTAAAACTT	NP_001193985.1:n.*252_*260delinsCTAAAACTT
NM_006892.3:c.*252_*260delinsCTAAAACTT , LRG_56t1:c.*252_*260delinsCTAAAACTT	NP_008823.1:n.*252_*260delinsCTAAAACTT
NM_175848.1:c.*252_*260delinsCTAAAACTT	NP_787044.1:n.*252_*260delinsCTAAAACTT
NM_175849.1:c.*252_*260delinsCTAAAACTT	NP_787045.1:n.*252_*260delinsCTAAAACTT
NM_175850.2:c.*252_*260delinsCTAAAACTT	NP_787046.1:n.*252_*260delinsCTAAAACTT
XM_011528653.1:c.*252_*260delinsCTAAAACTT	XP_011526955.1:n.*252_*260delinsCTAAAACTT
XM_011528654.1:c.*252_*260delinsCTAAAACTT	XP_011526956.1:n.*252_*260delinsCTAAAACTT
XR_936511.1:n.2592_2600delinsCTAAAACTT
XM_011528653.2:c.*252_*260delinsCTAAAACTT	XP_011526955.1:n.*252_*260delinsCTAAAACTT
XM_011528654.2:c.*252_*260delinsCTAAAACTT	XP_011526956.1:n.*252_*260delinsCTAAAACTT
XR_936511.2:n.2603_2611delinsCTAAAACTT
NM_001207055.2:c.*252_*260delinsCTAAAACTT	NP_001193984.1:n.*252_*260delinsCTAAAACTT
NM_001207056.2:c.*252_*260delinsCTAAAACTT	NP_001193985.1:n.*252_*260delinsCTAAAACTT
NM_006892.4:c.*252_*260delinsCTAAAACTT MANE Select	NP_008823.1:n.*252_*260delinsCTAAAACTT
NM_175848.2:c.*252_*260delinsCTAAAACTT	NP_787044.1:n.*252_*260delinsCTAAAACTT
NM_175849.2:c.*252_*260delinsCTAAAACTT	NP_787045.1:n.*252_*260delinsCTAAAACTT
NM_175850.3:c.*252_*260delinsCTAAAACTT	NP_787046.1:n.*252_*260delinsCTAAAACTT