Canonical Allele Identifier: CA2577367915

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807868_32807869insGAAG , CM000682.2:g.32807868_32807869insGAAG	GRCh38
NC_000020.10:g.31395674_31395675insGAAG , CM000682.1:g.31395674_31395675insGAAG	GRCh37
NC_000020.9:g.30859335_30859336insGAAG	NCBI36
NG_007290.1:g.50484_50485insGAAG , LRG_56:g.50484_50485insGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1478_*1479insGAAG	ENSP00000512497.1:n.*1478_*1479insGAAG
ENST00000696232.1:c.2338_2339insGAAG	ENSP00000512498.1:p.Phe780Ter
ENST00000696233.1:c.*1081_*1082insGAAG	ENSP00000512499.1:n.*1081_*1082insGAAG
ENST00000696238.1:c.*1270_*1271insGAAG	ENSP00000512502.1:n.*1270_*1271insGAAG
ENST00000696239.1:c.2308_2309insGAAG	ENSP00000512503.1:p.Phe770Ter
ENST00000696245.1:n.552_553insGAAG
ENST00000201963.3:c.2503_2504insGAAG	ENSP00000201963.3:p.Phe835Ter
ENST00000328111.6:c.2527_2528insGAAG MANE Select	ENSP00000328547.2:p.Phe843Ter
ENST00000348286.6:c.2278_2279insGAAG	ENSP00000337764.2:p.Phe760Ter
ENST00000353855.6:c.2467_2468insGAAG	ENSP00000313397.4:p.Phe823Ter
ENST00000443239.7:c.2152_2153insGAAG	ENSP00000403169.2:p.Phe718Ter
ENST00000456297.6:c.2050_2051insGAAG	ENSP00000412305.1:p.Phe684Ter
NM_001207055.1:c.2152_2153insGAAG	NP_001193984.1:p.Phe718Ter
NM_001207056.1:c.2050_2051insGAAG	NP_001193985.1:p.Phe684Ter
NM_006892.3:c.2527_2528insGAAG , LRG_56t1:c.2527_2528insGAAG	NP_008823.1:p.Phe843Ter
NM_175848.1:c.2467_2468insGAAG	NP_787044.1:p.Phe823Ter
NM_175849.1:c.2278_2279insGAAG	NP_787045.1:p.Phe760Ter
NM_175850.2:c.2503_2504insGAAG	NP_787046.1:p.Phe835Ter
XM_011528653.1:c.2314_2315insGAAG	XP_011526955.1:p.Phe772Ter
XM_011528654.1:c.2188_2189insGAAG	XP_011526956.1:p.Phe730Ter
XR_936511.1:n.2305_2306insGAAG
XM_011528653.2:c.2314_2315insGAAG	XP_011526955.1:p.Phe772Ter
XM_011528654.2:c.2188_2189insGAAG	XP_011526956.1:p.Phe730Ter
XR_936511.2:n.2316_2317insGAAG
NM_001207055.2:c.2152_2153insGAAG	NP_001193984.1:p.Phe718Ter
NM_001207056.2:c.2050_2051insGAAG	NP_001193985.1:p.Phe684Ter
NM_006892.4:c.2527_2528insGAAG MANE Select	NP_008823.1:p.Phe843Ter
NM_175848.2:c.2467_2468insGAAG	NP_787044.1:p.Phe823Ter
NM_175849.2:c.2278_2279insGAAG	NP_787045.1:p.Phe760Ter
NM_175850.3:c.2503_2504insGAAG	NP_787046.1:p.Phe835Ter