Canonical Allele Identifier: CA2652396149

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32787143-TGCCTAGGAGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32787144_32787153del , CM000682.2:g.32787144_32787153del	GRCh38
NC_000020.10:g.31374950_31374959del , CM000682.1:g.31374950_31374959del	GRCh37
NC_000020.9:g.30838611_30838620del	NCBI36
NG_007290.1:g.29760_29769del , LRG_56:g.29760_29769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.433-86_433-77del	ENSP00000512497.1:n.433-86_433-77del
ENST00000696232.1:c.433-86_433-77del	ENSP00000512498.1:n.433-86_433-77del
ENST00000696233.1:c.433-86_433-77del	ENSP00000512499.1:n.433-86_433-77del
ENST00000696234.1:n.417-86_417-77del
ENST00000696235.1:c.307-86_307-77del	ENSP00000512500.1:n.307-86_307-77del
ENST00000696236.1:c.307-86_307-77del	ENSP00000512501.1:n.307-86_307-77del
ENST00000696237.1:n.539-86_539-77del
ENST00000696238.1:c.433-86_433-77del	ENSP00000512502.1:n.433-86_433-77del
ENST00000696239.1:c.433-86_433-77del	ENSP00000512503.1:n.433-86_433-77del
ENST00000201963.3:c.469-86_469-77del	ENSP00000201963.3:n.469-86_469-77del
ENST00000328111.6:c.433-86_433-77del MANE Select	ENSP00000328547.2:n.433-86_433-77del
ENST00000348286.6:c.433-86_433-77del	ENSP00000337764.2:n.433-86_433-77del
ENST00000353855.6:c.433-86_433-77del	ENSP00000313397.4:n.433-86_433-77del
ENST00000443239.7:c.307-86_307-77del	ENSP00000403169.2:n.307-86_307-77del
ENST00000456297.6:c.205-86_205-77del	ENSP00000412305.1:n.205-86_205-77del
NM_001207055.1:c.307-86_307-77del	NP_001193984.1:n.307-86_307-77del
NM_001207056.1:c.205-86_205-77del	NP_001193985.1:n.205-86_205-77del
NM_006892.3:c.433-86_433-77del , LRG_56t1:c.433-86_433-77del	NP_008823.1:n.433-86_433-77del
NM_175848.1:c.433-86_433-77del	NP_787044.1:n.433-86_433-77del
NM_175849.1:c.433-86_433-77del	NP_787045.1:n.433-86_433-77del
NM_175850.2:c.469-86_469-77del	NP_787046.1:n.469-86_469-77del
XM_011528653.1:c.469-86_469-77del	XP_011526955.1:n.469-86_469-77del
XM_011528654.1:c.343-86_343-77del	XP_011526956.1:n.343-86_343-77del
XR_936510.1:n.605-86_605-77del
XR_936511.1:n.605-86_605-77del
XR_936512.1:n.480-86_480-77del
XM_011528653.2:c.469-86_469-77del	XP_011526955.1:n.469-86_469-77del
XM_011528654.2:c.343-86_343-77del	XP_011526956.1:n.343-86_343-77del
XR_936510.2:n.616-86_616-77del
XR_936511.2:n.616-86_616-77del
XR_936512.2:n.492-86_492-77del
NM_001207055.2:c.307-86_307-77del	NP_001193984.1:n.307-86_307-77del
NM_001207056.2:c.205-86_205-77del	NP_001193985.1:n.205-86_205-77del
NM_006892.4:c.433-86_433-77del MANE Select	NP_008823.1:n.433-86_433-77del
NM_175848.2:c.433-86_433-77del	NP_787044.1:n.433-86_433-77del
NM_175849.2:c.433-86_433-77del	NP_787045.1:n.433-86_433-77del
NM_175850.3:c.469-86_469-77del	NP_787046.1:n.469-86_469-77del