Canonical Allele Identifier: CA2652423196

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32805457-TGGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805458_32805461del , CM000682.2:g.32805458_32805461del	GRCh38
NC_000020.10:g.31393264_31393267del , CM000682.1:g.31393264_31393267del	GRCh37
NC_000020.9:g.30856925_30856928del	NCBI36
NG_007290.1:g.48074_48077del , LRG_56:g.48074_48077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+51_*1252+54del	ENSP00000512497.1:n.*1252+51_*1252+54del
ENST00000696232.1:c.2232-2304_2232-2301del	ENSP00000512498.1:n.2232-2304_2232-2301del
ENST00000696233.1:c.*975-2304_*975-2301del	ENSP00000512499.1:n.*975-2304_*975-2301del
ENST00000696238.1:c.*1044+51_*1044+54del	ENSP00000512502.1:n.*1044+51_*1044+54del
ENST00000696239.1:c.2082+51_2082+54del	ENSP00000512503.1:n.2082+51_2082+54del
ENST00000696245.1:n.327-751_327-748del
ENST00000201963.3:c.2277+51_2277+54del	ENSP00000201963.3:n.2277+51_2277+54del
ENST00000328111.6:c.2301+51_2301+54del MANE Select	ENSP00000328547.2:n.2301+51_2301+54del
ENST00000348286.6:c.2172-2304_2172-2301del	ENSP00000337764.2:n.2172-2304_2172-2301del
ENST00000353855.6:c.2241+51_2241+54del	ENSP00000313397.4:n.2241+51_2241+54del
ENST00000443239.7:c.2046-2304_2046-2301del	ENSP00000403169.2:n.2046-2304_2046-2301del
ENST00000456297.6:c.1944-2304_1944-2301del	ENSP00000412305.1:n.1944-2304_1944-2301del
NM_001207055.1:c.2046-2304_2046-2301del	NP_001193984.1:n.2046-2304_2046-2301del
NM_001207056.1:c.1944-2304_1944-2301del	NP_001193985.1:n.1944-2304_1944-2301del
NM_006892.3:c.2301+51_2301+54del , LRG_56t1:c.2301+51_2301+54del	NP_008823.1:n.2301+51_2301+54del
NM_175848.1:c.2241+51_2241+54del	NP_787044.1:n.2241+51_2241+54del
NM_175849.1:c.2172-2304_2172-2301del	NP_787045.1:n.2172-2304_2172-2301del
NM_175850.2:c.2277+51_2277+54del	NP_787046.1:n.2277+51_2277+54del
XM_011528653.1:c.2208-2304_2208-2301del	XP_011526955.1:n.2208-2304_2208-2301del
XM_011528654.1:c.2082-2304_2082-2301del	XP_011526956.1:n.2082-2304_2082-2301del
XR_936510.1:n.2268+51_2268+54del
XR_936511.1:n.2199-2304_2199-2301del
XR_936512.1:n.2143+51_2143+54del
XM_011528653.2:c.2208-2304_2208-2301del	XP_011526955.1:n.2208-2304_2208-2301del
XM_011528654.2:c.2082-2304_2082-2301del	XP_011526956.1:n.2082-2304_2082-2301del
XR_936510.2:n.2279+51_2279+54del
XR_936511.2:n.2210-2304_2210-2301del
XR_936512.2:n.2155+51_2155+54del
NM_001207055.2:c.2046-2304_2046-2301del	NP_001193984.1:n.2046-2304_2046-2301del
NM_001207056.2:c.1944-2304_1944-2301del	NP_001193985.1:n.1944-2304_1944-2301del
NM_006892.4:c.2301+51_2301+54del MANE Select	NP_008823.1:n.2301+51_2301+54del
NM_175848.2:c.2241+51_2241+54del	NP_787044.1:n.2241+51_2241+54del
NM_175849.2:c.2172-2304_2172-2301del	NP_787045.1:n.2172-2304_2172-2301del
NM_175850.3:c.2277+51_2277+54del	NP_787046.1:n.2277+51_2277+54del