Canonical Allele Identifier: CA2360466366

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32808191_32808193delinsCTT , CM000682.2:g.32808191_32808193delinsCTT	GRCh38
NC_000020.10:g.31395997_31395999delinsCTT , CM000682.1:g.31395997_31395999delinsCTT	GRCh37
NC_000020.9:g.30859658_30859660delinsCTT	NCBI36
NG_007290.1:g.50807_50809delinsCTT , LRG_56:g.50807_50809delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1801_*1803delinsCTT	ENSP00000512497.1:n.*1801_*1803delinsCTT
ENST00000696232.1:c.*288_*290delinsCTT	ENSP00000512498.1:n.*288_*290delinsCTT
ENST00000696233.1:c.*1404_*1406delinsCTT	ENSP00000512499.1:n.*1404_*1406delinsCTT
ENST00000696238.1:c.*1593_*1595delinsCTT	ENSP00000512502.1:n.*1593_*1595delinsCTT
ENST00000696245.1:n.875_877delinsCTT
ENST00000201963.3:c.*288_*290delinsCTT	ENSP00000201963.3:n.*288_*290delinsCTT
ENST00000328111.6:c.*288_*290delinsCTT MANE Select	ENSP00000328547.2:n.*288_*290delinsCTT
ENST00000348286.6:c.*288_*290delinsCTT	ENSP00000337764.2:n.*288_*290delinsCTT
ENST00000353855.6:c.*288_*290delinsCTT	ENSP00000313397.4:n.*288_*290delinsCTT
ENST00000443239.7:c.*288_*290delinsCTT	ENSP00000403169.2:n.*288_*290delinsCTT
NM_001207055.1:c.*288_*290delinsCTT	NP_001193984.1:n.*288_*290delinsCTT
NM_001207056.1:c.*288_*290delinsCTT	NP_001193985.1:n.*288_*290delinsCTT
NM_006892.3:c.*288_*290delinsCTT , LRG_56t1:c.*288_*290delinsCTT	NP_008823.1:n.*288_*290delinsCTT
NM_175848.1:c.*288_*290delinsCTT	NP_787044.1:n.*288_*290delinsCTT
NM_175849.1:c.*288_*290delinsCTT	NP_787045.1:n.*288_*290delinsCTT
NM_175850.2:c.*288_*290delinsCTT	NP_787046.1:n.*288_*290delinsCTT
XM_011528653.1:c.*288_*290delinsCTT	XP_011526955.1:n.*288_*290delinsCTT
XM_011528654.1:c.*288_*290delinsCTT	XP_011526956.1:n.*288_*290delinsCTT
XR_936511.1:n.2628_2630delinsCTT
XM_011528653.2:c.*288_*290delinsCTT	XP_011526955.1:n.*288_*290delinsCTT
XM_011528654.2:c.*288_*290delinsCTT	XP_011526956.1:n.*288_*290delinsCTT
XR_936511.2:n.2639_2641delinsCTT
NM_001207055.2:c.*288_*290delinsCTT	NP_001193984.1:n.*288_*290delinsCTT
NM_001207056.2:c.*288_*290delinsCTT	NP_001193985.1:n.*288_*290delinsCTT
NM_006892.4:c.*288_*290delinsCTT MANE Select	NP_008823.1:n.*288_*290delinsCTT
NM_175848.2:c.*288_*290delinsCTT	NP_787044.1:n.*288_*290delinsCTT
NM_175849.2:c.*288_*290delinsCTT	NP_787045.1:n.*288_*290delinsCTT
NM_175850.3:c.*288_*290delinsCTT	NP_787046.1:n.*288_*290delinsCTT