Canonical Allele Identifier: CA2534714157

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805518_32805519insGGAAGAG , CM000682.2:g.32805518_32805519insGGAAGAG	GRCh38
NC_000020.10:g.31393324_31393325insGGAAGAG , CM000682.1:g.31393324_31393325insGGAAGAG	GRCh37
NC_000020.9:g.30856985_30856986insGGAAGAG	NCBI36
NG_007290.1:g.48134_48135insGGAAGAG , LRG_56:g.48134_48135insGGAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1252+111_*1252+112insGGAAGAG	ENSP00000512497.1:n.*1252+111_*1252+112insGGAAGAG
ENST00000696232.1:c.2232-2244_2232-2243insGGAAGAG	ENSP00000512498.1:n.2232-2244_2232-2243insGGAAGAG
ENST00000696233.1:c.*975-2244_*975-2243insGGAAGAG	ENSP00000512499.1:n.*975-2244_*975-2243insGGAAGAG
ENST00000696238.1:c.*1044+111_*1044+112insGGAAGAG	ENSP00000512502.1:n.*1044+111_*1044+112insGGAAGAG
ENST00000696239.1:c.2082+111_2082+112insGGAAGAG	ENSP00000512503.1:n.2082+111_2082+112insGGAAGAG
ENST00000696245.1:n.327-691_327-690insGGAAGAG
ENST00000201963.3:c.2277+111_2277+112insGGAAGAG	ENSP00000201963.3:n.2277+111_2277+112insGGAAGAG
ENST00000328111.6:c.2301+111_2301+112insGGAAGAG MANE Select	ENSP00000328547.2:n.2301+111_2301+112insGGAAGAG
ENST00000348286.6:c.2172-2244_2172-2243insGGAAGAG	ENSP00000337764.2:n.2172-2244_2172-2243insGGAAGAG
ENST00000353855.6:c.2241+111_2241+112insGGAAGAG	ENSP00000313397.4:n.2241+111_2241+112insGGAAGAG
ENST00000443239.7:c.2046-2244_2046-2243insGGAAGAG	ENSP00000403169.2:n.2046-2244_2046-2243insGGAAGAG
ENST00000456297.6:c.1944-2244_1944-2243insGGAAGAG	ENSP00000412305.1:n.1944-2244_1944-2243insGGAAGAG
NM_001207055.1:c.2046-2244_2046-2243insGGAAGAG	NP_001193984.1:n.2046-2244_2046-2243insGGAAGAG
NM_001207056.1:c.1944-2244_1944-2243insGGAAGAG	NP_001193985.1:n.1944-2244_1944-2243insGGAAGAG
NM_006892.3:c.2301+111_2301+112insGGAAGAG , LRG_56t1:c.2301+111_2301+112insGGAAGAG	NP_008823.1:n.2301+111_2301+112insGGAAGAG
NM_175848.1:c.2241+111_2241+112insGGAAGAG	NP_787044.1:n.2241+111_2241+112insGGAAGAG
NM_175849.1:c.2172-2244_2172-2243insGGAAGAG	NP_787045.1:n.2172-2244_2172-2243insGGAAGAG
NM_175850.2:c.2277+111_2277+112insGGAAGAG	NP_787046.1:n.2277+111_2277+112insGGAAGAG
XM_011528653.1:c.2208-2244_2208-2243insGGAAGAG	XP_011526955.1:n.2208-2244_2208-2243insGGAAGAG
XM_011528654.1:c.2082-2244_2082-2243insGGAAGAG	XP_011526956.1:n.2082-2244_2082-2243insGGAAGAG
XR_936510.1:n.2268+111_2268+112insGGAAGAG
XR_936511.1:n.2199-2244_2199-2243insGGAAGAG
XR_936512.1:n.2143+111_2143+112insGGAAGAG
XM_011528653.2:c.2208-2244_2208-2243insGGAAGAG	XP_011526955.1:n.2208-2244_2208-2243insGGAAGAG
XM_011528654.2:c.2082-2244_2082-2243insGGAAGAG	XP_011526956.1:n.2082-2244_2082-2243insGGAAGAG
XR_936510.2:n.2279+111_2279+112insGGAAGAG
XR_936511.2:n.2210-2244_2210-2243insGGAAGAG
XR_936512.2:n.2155+111_2155+112insGGAAGAG
NM_001207055.2:c.2046-2244_2046-2243insGGAAGAG	NP_001193984.1:n.2046-2244_2046-2243insGGAAGAG
NM_001207056.2:c.1944-2244_1944-2243insGGAAGAG	NP_001193985.1:n.1944-2244_1944-2243insGGAAGAG
NM_006892.4:c.2301+111_2301+112insGGAAGAG MANE Select	NP_008823.1:n.2301+111_2301+112insGGAAGAG
NM_175848.2:c.2241+111_2241+112insGGAAGAG	NP_787044.1:n.2241+111_2241+112insGGAAGAG
NM_175849.2:c.2172-2244_2172-2243insGGAAGAG	NP_787045.1:n.2172-2244_2172-2243insGGAAGAG
NM_175850.3:c.2277+111_2277+112insGGAAGAG	NP_787046.1:n.2277+111_2277+112insGGAAGAG