Canonical Allele Identifier: CA2360465190

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805483_32805487delinsTTTGA , CM000682.2:g.32805483_32805487delinsTTTGA	GRCh38
NC_000020.10:g.31393289_31393293delinsTTTGA , CM000682.1:g.31393289_31393293delinsTTTGA	GRCh37
NC_000020.9:g.30856950_30856954delinsTTTGA	NCBI36
NG_007290.1:g.48099_48103delinsTTTGA , LRG_56:g.48099_48103delinsTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+76_*1252+80delinsTTTGA	ENSP00000512497.1:n.*1252+76_*1252+80delinsTTTGA
ENST00000696232.1:c.2232-2279_2232-2275delinsTTTGA	ENSP00000512498.1:n.2232-2279_2232-2275delinsTTTGA
ENST00000696233.1:c.*975-2279_*975-2275delinsTTTGA	ENSP00000512499.1:n.*975-2279_*975-2275delinsTTTGA
ENST00000696238.1:c.*1044+76_*1044+80delinsTTTGA	ENSP00000512502.1:n.*1044+76_*1044+80delinsTTTGA
ENST00000696239.1:c.2082+76_2082+80delinsTTTGA	ENSP00000512503.1:n.2082+76_2082+80delinsTTTGA
ENST00000696245.1:n.327-726_327-722delinsTTTGA
ENST00000201963.3:c.2277+76_2277+80delinsTTTGA	ENSP00000201963.3:n.2277+76_2277+80delinsTTTGA
ENST00000328111.6:c.2301+76_2301+80delinsTTTGA MANE Select	ENSP00000328547.2:n.2301+76_2301+80delinsTTTGA
ENST00000348286.6:c.2172-2279_2172-2275delinsTTTGA	ENSP00000337764.2:n.2172-2279_2172-2275delinsTTTGA
ENST00000353855.6:c.2241+76_2241+80delinsTTTGA	ENSP00000313397.4:n.2241+76_2241+80delinsTTTGA
ENST00000443239.7:c.2046-2279_2046-2275delinsTTTGA	ENSP00000403169.2:n.2046-2279_2046-2275delinsTTTGA
ENST00000456297.6:c.1944-2279_1944-2275delinsTTTGA	ENSP00000412305.1:n.1944-2279_1944-2275delinsTTTGA
NM_001207055.1:c.2046-2279_2046-2275delinsTTTGA	NP_001193984.1:n.2046-2279_2046-2275delinsTTTGA
NM_001207056.1:c.1944-2279_1944-2275delinsTTTGA	NP_001193985.1:n.1944-2279_1944-2275delinsTTTGA
NM_006892.3:c.2301+76_2301+80delinsTTTGA , LRG_56t1:c.2301+76_2301+80delinsTTTGA	NP_008823.1:n.2301+76_2301+80delinsTTTGA
NM_175848.1:c.2241+76_2241+80delinsTTTGA	NP_787044.1:n.2241+76_2241+80delinsTTTGA
NM_175849.1:c.2172-2279_2172-2275delinsTTTGA	NP_787045.1:n.2172-2279_2172-2275delinsTTTGA
NM_175850.2:c.2277+76_2277+80delinsTTTGA	NP_787046.1:n.2277+76_2277+80delinsTTTGA
XM_011528653.1:c.2208-2279_2208-2275delinsTTTGA	XP_011526955.1:n.2208-2279_2208-2275delinsTTTGA
XM_011528654.1:c.2082-2279_2082-2275delinsTTTGA	XP_011526956.1:n.2082-2279_2082-2275delinsTTTGA
XR_936510.1:n.2268+76_2268+80delinsTTTGA
XR_936511.1:n.2199-2279_2199-2275delinsTTTGA
XR_936512.1:n.2143+76_2143+80delinsTTTGA
XM_011528653.2:c.2208-2279_2208-2275delinsTTTGA	XP_011526955.1:n.2208-2279_2208-2275delinsTTTGA
XM_011528654.2:c.2082-2279_2082-2275delinsTTTGA	XP_011526956.1:n.2082-2279_2082-2275delinsTTTGA
XR_936510.2:n.2279+76_2279+80delinsTTTGA
XR_936511.2:n.2210-2279_2210-2275delinsTTTGA
XR_936512.2:n.2155+76_2155+80delinsTTTGA
NM_001207055.2:c.2046-2279_2046-2275delinsTTTGA	NP_001193984.1:n.2046-2279_2046-2275delinsTTTGA
NM_001207056.2:c.1944-2279_1944-2275delinsTTTGA	NP_001193985.1:n.1944-2279_1944-2275delinsTTTGA
NM_006892.4:c.2301+76_2301+80delinsTTTGA MANE Select	NP_008823.1:n.2301+76_2301+80delinsTTTGA
NM_175848.2:c.2241+76_2241+80delinsTTTGA	NP_787044.1:n.2241+76_2241+80delinsTTTGA
NM_175849.2:c.2172-2279_2172-2275delinsTTTGA	NP_787045.1:n.2172-2279_2172-2275delinsTTTGA
NM_175850.3:c.2277+76_2277+80delinsTTTGA	NP_787046.1:n.2277+76_2277+80delinsTTTGA