Canonical Allele Identifier: CA2652425840

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32800299-GTGAGGGCAGTCTGTACCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32800302_32800319del , CM000682.2:g.32800302_32800319del	GRCh38
NC_000020.10:g.31388108_31388125del , CM000682.1:g.31388108_31388125del	GRCh37
NC_000020.9:g.30851769_30851786del	NCBI36
NG_007290.1:g.42918_42935del , LRG_56:g.42918_42935del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*856+4_*856+21del	ENSP00000512497.1:n.*856+4_*856+21del
ENST00000696232.1:c.1905+4_1905+21del	ENSP00000512498.1:n.1905+4_1905+21del
ENST00000696233.1:c.*648+4_*648+21del	ENSP00000512499.1:n.*648+4_*648+21del
ENST00000696235.1:c.*553+4_*553+21del	ENSP00000512500.1:n.*553+4_*553+21del
ENST00000696238.1:c.*648+4_*648+21del	ENSP00000512502.1:n.*648+4_*648+21del
ENST00000696239.1:c.1686+4_1686+21del	ENSP00000512503.1:n.1686+4_1686+21del
ENST00000201963.3:c.1881+4_1881+21del	ENSP00000201963.3:n.1881+4_1881+21del
ENST00000328111.6:c.1905+4_1905+21del MANE Select	ENSP00000328547.2:n.1905+4_1905+21del
ENST00000348286.6:c.1845+4_1845+21del	ENSP00000337764.2:n.1845+4_1845+21del
ENST00000353855.6:c.1845+4_1845+21del	ENSP00000313397.4:n.1845+4_1845+21del
ENST00000443239.7:c.1719+4_1719+21del	ENSP00000403169.2:n.1719+4_1719+21del
ENST00000456297.6:c.1617+4_1617+21del	ENSP00000412305.1:n.1617+4_1617+21del
NM_001207055.1:c.1719+4_1719+21del	NP_001193984.1:n.1719+4_1719+21del
NM_001207056.1:c.1617+4_1617+21del	NP_001193985.1:n.1617+4_1617+21del
NM_006892.3:c.1905+4_1905+21del , LRG_56t1:c.1905+4_1905+21del	NP_008823.1:n.1905+4_1905+21del
NM_175848.1:c.1845+4_1845+21del	NP_787044.1:n.1845+4_1845+21del
NM_175849.1:c.1845+4_1845+21del	NP_787045.1:n.1845+4_1845+21del
NM_175850.2:c.1881+4_1881+21del	NP_787046.1:n.1881+4_1881+21del
XM_011528653.1:c.1881+4_1881+21del	XP_011526955.1:n.1881+4_1881+21del
XM_011528654.1:c.1755+4_1755+21del	XP_011526956.1:n.1755+4_1755+21del
XR_936510.1:n.1872+4_1872+21del
XR_936511.1:n.1872+4_1872+21del
XR_936512.1:n.1747+4_1747+21del
XM_011528653.2:c.1881+4_1881+21del	XP_011526955.1:n.1881+4_1881+21del
XM_011528654.2:c.1755+4_1755+21del	XP_011526956.1:n.1755+4_1755+21del
XR_936510.2:n.1883+4_1883+21del
XR_936511.2:n.1883+4_1883+21del
XR_936512.2:n.1759+4_1759+21del
NM_001207055.2:c.1719+4_1719+21del	NP_001193984.1:n.1719+4_1719+21del
NM_001207056.2:c.1617+4_1617+21del	NP_001193985.1:n.1617+4_1617+21del
NM_006892.4:c.1905+4_1905+21del MANE Select	NP_008823.1:n.1905+4_1905+21del
NM_175848.2:c.1845+4_1845+21del	NP_787044.1:n.1845+4_1845+21del
NM_175849.2:c.1845+4_1845+21del	NP_787045.1:n.1845+4_1845+21del
NM_175850.3:c.1881+4_1881+21del	NP_787046.1:n.1881+4_1881+21del