Canonical Allele Identifier: CA2652423279

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32805547-ATTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805550_32805552del , CM000682.2:g.32805550_32805552del	GRCh38
NC_000020.10:g.31393356_31393358del , CM000682.1:g.31393356_31393358del	GRCh37
NC_000020.9:g.30857017_30857019del	NCBI36
NG_007290.1:g.48166_48168del , LRG_56:g.48166_48168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+143_*1252+145del	ENSP00000512497.1:n.*1252+143_*1252+145del
ENST00000696232.1:c.2232-2212_2232-2210del	ENSP00000512498.1:n.2232-2212_2232-2210del
ENST00000696233.1:c.*975-2212_*975-2210del	ENSP00000512499.1:n.*975-2212_*975-2210del
ENST00000696238.1:c.*1044+143_*1044+145del	ENSP00000512502.1:n.*1044+143_*1044+145del
ENST00000696239.1:c.2082+143_2082+145del	ENSP00000512503.1:n.2082+143_2082+145del
ENST00000696245.1:n.327-659_327-657del
ENST00000201963.3:c.2277+143_2277+145del	ENSP00000201963.3:n.2277+143_2277+145del
ENST00000328111.6:c.2301+143_2301+145del MANE Select	ENSP00000328547.2:n.2301+143_2301+145del
ENST00000348286.6:c.2172-2212_2172-2210del	ENSP00000337764.2:n.2172-2212_2172-2210del
ENST00000353855.6:c.2241+143_2241+145del	ENSP00000313397.4:n.2241+143_2241+145del
ENST00000443239.7:c.2046-2212_2046-2210del	ENSP00000403169.2:n.2046-2212_2046-2210del
ENST00000456297.6:c.1944-2212_1944-2210del	ENSP00000412305.1:n.1944-2212_1944-2210del
NM_001207055.1:c.2046-2212_2046-2210del	NP_001193984.1:n.2046-2212_2046-2210del
NM_001207056.1:c.1944-2212_1944-2210del	NP_001193985.1:n.1944-2212_1944-2210del
NM_006892.3:c.2301+143_2301+145del , LRG_56t1:c.2301+143_2301+145del	NP_008823.1:n.2301+143_2301+145del
NM_175848.1:c.2241+143_2241+145del	NP_787044.1:n.2241+143_2241+145del
NM_175849.1:c.2172-2212_2172-2210del	NP_787045.1:n.2172-2212_2172-2210del
NM_175850.2:c.2277+143_2277+145del	NP_787046.1:n.2277+143_2277+145del
XM_011528653.1:c.2208-2212_2208-2210del	XP_011526955.1:n.2208-2212_2208-2210del
XM_011528654.1:c.2082-2212_2082-2210del	XP_011526956.1:n.2082-2212_2082-2210del
XR_936510.1:n.2268+143_2268+145del
XR_936511.1:n.2199-2212_2199-2210del
XR_936512.1:n.2143+143_2143+145del
XM_011528653.2:c.2208-2212_2208-2210del	XP_011526955.1:n.2208-2212_2208-2210del
XM_011528654.2:c.2082-2212_2082-2210del	XP_011526956.1:n.2082-2212_2082-2210del
XR_936510.2:n.2279+143_2279+145del
XR_936511.2:n.2210-2212_2210-2210del
XR_936512.2:n.2155+143_2155+145del
NM_001207055.2:c.2046-2212_2046-2210del	NP_001193984.1:n.2046-2212_2046-2210del
NM_001207056.2:c.1944-2212_1944-2210del	NP_001193985.1:n.1944-2212_1944-2210del
NM_006892.4:c.2301+143_2301+145del MANE Select	NP_008823.1:n.2301+143_2301+145del
NM_175848.2:c.2241+143_2241+145del	NP_787044.1:n.2241+143_2241+145del
NM_175849.2:c.2172-2212_2172-2210del	NP_787045.1:n.2172-2212_2172-2210del
NM_175850.3:c.2277+143_2277+145del	NP_787046.1:n.2277+143_2277+145del