Canonical Allele Identifier: CA2816162898

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787152_32787153insTTTTTTTTTT , CM000682.2:g.32787152_32787153insTTTTTTTTTT	GRCh38
NC_000020.10:g.31374958_31374959insTTTTTTTTTT , CM000682.1:g.31374958_31374959insTTTTTTTTTT	GRCh37
NC_000020.9:g.30838619_30838620insTTTTTTTTTT	NCBI36
NG_007290.1:g.29768_29769insTTTTTTTTTT , LRG_56:g.29768_29769insTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.433-78_433-77insTTTTTTTTTT	ENSP00000512497.1:n.433-78_433-77insTTTTTTTTTT
ENST00000696232.1:c.433-78_433-77insTTTTTTTTTT	ENSP00000512498.1:n.433-78_433-77insTTTTTTTTTT
ENST00000696233.1:c.433-78_433-77insTTTTTTTTTT	ENSP00000512499.1:n.433-78_433-77insTTTTTTTTTT
ENST00000696234.1:n.417-78_417-77insTTTTTTTTTT
ENST00000696235.1:c.307-78_307-77insTTTTTTTTTT	ENSP00000512500.1:n.307-78_307-77insTTTTTTTTTT
ENST00000696236.1:c.307-78_307-77insTTTTTTTTTT	ENSP00000512501.1:n.307-78_307-77insTTTTTTTTTT
ENST00000696237.1:n.539-78_539-77insTTTTTTTTTT
ENST00000696238.1:c.433-78_433-77insTTTTTTTTTT	ENSP00000512502.1:n.433-78_433-77insTTTTTTTTTT
ENST00000696239.1:c.433-78_433-77insTTTTTTTTTT	ENSP00000512503.1:n.433-78_433-77insTTTTTTTTTT
ENST00000201963.3:c.469-78_469-77insTTTTTTTTTT	ENSP00000201963.3:n.469-78_469-77insTTTTTTTTTT
ENST00000328111.6:c.433-78_433-77insTTTTTTTTTT MANE Select	ENSP00000328547.2:n.433-78_433-77insTTTTTTTTTT
ENST00000348286.6:c.433-78_433-77insTTTTTTTTTT	ENSP00000337764.2:n.433-78_433-77insTTTTTTTTTT
ENST00000353855.6:c.433-78_433-77insTTTTTTTTTT	ENSP00000313397.4:n.433-78_433-77insTTTTTTTTTT
ENST00000443239.7:c.307-78_307-77insTTTTTTTTTT	ENSP00000403169.2:n.307-78_307-77insTTTTTTTTTT
ENST00000456297.6:c.205-78_205-77insTTTTTTTTTT	ENSP00000412305.1:n.205-78_205-77insTTTTTTTTTT
NM_001207055.1:c.307-78_307-77insTTTTTTTTTT	NP_001193984.1:n.307-78_307-77insTTTTTTTTTT
NM_001207056.1:c.205-78_205-77insTTTTTTTTTT	NP_001193985.1:n.205-78_205-77insTTTTTTTTTT
NM_006892.3:c.433-78_433-77insTTTTTTTTTT , LRG_56t1:c.433-78_433-77insTTTTTTTTTT	NP_008823.1:n.433-78_433-77insTTTTTTTTTT
NM_175848.1:c.433-78_433-77insTTTTTTTTTT	NP_787044.1:n.433-78_433-77insTTTTTTTTTT
NM_175849.1:c.433-78_433-77insTTTTTTTTTT	NP_787045.1:n.433-78_433-77insTTTTTTTTTT
NM_175850.2:c.469-78_469-77insTTTTTTTTTT	NP_787046.1:n.469-78_469-77insTTTTTTTTTT
XM_011528653.1:c.469-78_469-77insTTTTTTTTTT	XP_011526955.1:n.469-78_469-77insTTTTTTTTTT
XM_011528654.1:c.343-78_343-77insTTTTTTTTTT	XP_011526956.1:n.343-78_343-77insTTTTTTTTTT
XR_936510.1:n.605-78_605-77insTTTTTTTTTT
XR_936511.1:n.605-78_605-77insTTTTTTTTTT
XR_936512.1:n.480-78_480-77insTTTTTTTTTT
XM_011528653.2:c.469-78_469-77insTTTTTTTTTT	XP_011526955.1:n.469-78_469-77insTTTTTTTTTT
XM_011528654.2:c.343-78_343-77insTTTTTTTTTT	XP_011526956.1:n.343-78_343-77insTTTTTTTTTT
XR_936510.2:n.616-78_616-77insTTTTTTTTTT
XR_936511.2:n.616-78_616-77insTTTTTTTTTT
XR_936512.2:n.492-78_492-77insTTTTTTTTTT
NM_001207055.2:c.307-78_307-77insTTTTTTTTTT	NP_001193984.1:n.307-78_307-77insTTTTTTTTTT
NM_001207056.2:c.205-78_205-77insTTTTTTTTTT	NP_001193985.1:n.205-78_205-77insTTTTTTTTTT
NM_006892.4:c.433-78_433-77insTTTTTTTTTT MANE Select	NP_008823.1:n.433-78_433-77insTTTTTTTTTT
NM_175848.2:c.433-78_433-77insTTTTTTTTTT	NP_787044.1:n.433-78_433-77insTTTTTTTTTT
NM_175849.2:c.433-78_433-77insTTTTTTTTTT	NP_787045.1:n.433-78_433-77insTTTTTTTTTT
NM_175850.3:c.469-78_469-77insTTTTTTTTTT	NP_787046.1:n.469-78_469-77insTTTTTTTTTT