Canonical Allele Identifier: CA2652423203

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32805497-ACTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805502_32805504del , CM000682.2:g.32805502_32805504del	GRCh38
NC_000020.10:g.31393308_31393310del , CM000682.1:g.31393308_31393310del	GRCh37
NC_000020.9:g.30856969_30856971del	NCBI36
NG_007290.1:g.48118_48120del , LRG_56:g.48118_48120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+95_*1252+97del	ENSP00000512497.1:n.*1252+95_*1252+97del
ENST00000696232.1:c.2232-2260_2232-2258del	ENSP00000512498.1:n.2232-2260_2232-2258del
ENST00000696233.1:c.*975-2260_*975-2258del	ENSP00000512499.1:n.*975-2260_*975-2258del
ENST00000696238.1:c.*1044+95_*1044+97del	ENSP00000512502.1:n.*1044+95_*1044+97del
ENST00000696239.1:c.2082+95_2082+97del	ENSP00000512503.1:n.2082+95_2082+97del
ENST00000696245.1:n.327-707_327-705del
ENST00000201963.3:c.2277+95_2277+97del	ENSP00000201963.3:n.2277+95_2277+97del
ENST00000328111.6:c.2301+95_2301+97del MANE Select	ENSP00000328547.2:n.2301+95_2301+97del
ENST00000348286.6:c.2172-2260_2172-2258del	ENSP00000337764.2:n.2172-2260_2172-2258del
ENST00000353855.6:c.2241+95_2241+97del	ENSP00000313397.4:n.2241+95_2241+97del
ENST00000443239.7:c.2046-2260_2046-2258del	ENSP00000403169.2:n.2046-2260_2046-2258del
ENST00000456297.6:c.1944-2260_1944-2258del	ENSP00000412305.1:n.1944-2260_1944-2258del
NM_001207055.1:c.2046-2260_2046-2258del	NP_001193984.1:n.2046-2260_2046-2258del
NM_001207056.1:c.1944-2260_1944-2258del	NP_001193985.1:n.1944-2260_1944-2258del
NM_006892.3:c.2301+95_2301+97del , LRG_56t1:c.2301+95_2301+97del	NP_008823.1:n.2301+95_2301+97del
NM_175848.1:c.2241+95_2241+97del	NP_787044.1:n.2241+95_2241+97del
NM_175849.1:c.2172-2260_2172-2258del	NP_787045.1:n.2172-2260_2172-2258del
NM_175850.2:c.2277+95_2277+97del	NP_787046.1:n.2277+95_2277+97del
XM_011528653.1:c.2208-2260_2208-2258del	XP_011526955.1:n.2208-2260_2208-2258del
XM_011528654.1:c.2082-2260_2082-2258del	XP_011526956.1:n.2082-2260_2082-2258del
XR_936510.1:n.2268+95_2268+97del
XR_936511.1:n.2199-2260_2199-2258del
XR_936512.1:n.2143+95_2143+97del
XM_011528653.2:c.2208-2260_2208-2258del	XP_011526955.1:n.2208-2260_2208-2258del
XM_011528654.2:c.2082-2260_2082-2258del	XP_011526956.1:n.2082-2260_2082-2258del
XR_936510.2:n.2279+95_2279+97del
XR_936511.2:n.2210-2260_2210-2258del
XR_936512.2:n.2155+95_2155+97del
NM_001207055.2:c.2046-2260_2046-2258del	NP_001193984.1:n.2046-2260_2046-2258del
NM_001207056.2:c.1944-2260_1944-2258del	NP_001193985.1:n.1944-2260_1944-2258del
NM_006892.4:c.2301+95_2301+97del MANE Select	NP_008823.1:n.2301+95_2301+97del
NM_175848.2:c.2241+95_2241+97del	NP_787044.1:n.2241+95_2241+97del
NM_175849.2:c.2172-2260_2172-2258del	NP_787045.1:n.2172-2260_2172-2258del
NM_175850.3:c.2277+95_2277+97del	NP_787046.1:n.2277+95_2277+97del