Canonical Allele Identifier: CA2652423788

Gene: DNMT3B

Linked Data

• gnomAD v4: 20-32807791-A-ACATGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32807792_32807793insATGGGCC , CM000682.2:g.32807792_32807793insATGGGCC	GRCh38
NC_000020.10:g.31395598_31395599insATGGGCC , CM000682.1:g.31395598_31395599insATGGGCC	GRCh37
NC_000020.9:g.30859259_30859260insATGGGCC	NCBI36
NG_007290.1:g.50408_50409insATGGGCC , LRG_56:g.50408_50409insATGGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1402_*1403insATGGGCC	ENSP00000512497.1:n.*1402_*1403insATGGGCC
ENST00000696232.1:c.2262_2263insATGGGCC	ENSP00000512498.1:p.Val755MetfsTer?
ENST00000696233.1:c.*1005_*1006insATGGGCC	ENSP00000512499.1:n.*1005_*1006insATGGGCC
ENST00000696238.1:c.*1194_*1195insATGGGCC	ENSP00000512502.1:n.*1194_*1195insATGGGCC
ENST00000696239.1:c.2232_2233insATGGGCC	ENSP00000512503.1:p.Val745MetfsTer?
ENST00000696245.1:n.476_477insATGGGCC
ENST00000201963.3:c.2427_2428insATGGGCC	ENSP00000201963.3:p.Val810MetfsTer?
ENST00000328111.6:c.2451_2452insATGGGCC MANE Select	ENSP00000328547.2:p.Val818MetfsTer?
ENST00000348286.6:c.2202_2203insATGGGCC	ENSP00000337764.2:p.Val735MetfsTer?
ENST00000353855.6:c.2391_2392insATGGGCC	ENSP00000313397.4:p.Val798MetfsTer?
ENST00000443239.7:c.2076_2077insATGGGCC	ENSP00000403169.2:p.Val693MetfsTer?
ENST00000456297.6:c.1974_1975insATGGGCC	ENSP00000412305.1:p.Val659MetfsTer?
NM_001207055.1:c.2076_2077insATGGGCC	NP_001193984.1:p.Val693MetfsTer?
NM_001207056.1:c.1974_1975insATGGGCC	NP_001193985.1:p.Val659MetfsTer?
NM_006892.3:c.2451_2452insATGGGCC , LRG_56t1:c.2451_2452insATGGGCC	NP_008823.1:p.Val818MetfsTer?
NM_175848.1:c.2391_2392insATGGGCC	NP_787044.1:p.Val798MetfsTer?
NM_175849.1:c.2202_2203insATGGGCC	NP_787045.1:p.Val735MetfsTer?
NM_175850.2:c.2427_2428insATGGGCC	NP_787046.1:p.Val810MetfsTer?
XM_011528653.1:c.2238_2239insATGGGCC	XP_011526955.1:p.Val747MetfsTer?
XM_011528654.1:c.2112_2113insATGGGCC	XP_011526956.1:p.Val705MetfsTer?
XR_936511.1:n.2229_2230insATGGGCC
XM_011528653.2:c.2238_2239insATGGGCC	XP_011526955.1:p.Val747MetfsTer?
XM_011528654.2:c.2112_2113insATGGGCC	XP_011526956.1:p.Val705MetfsTer?
XR_936511.2:n.2240_2241insATGGGCC
NM_001207055.2:c.2076_2077insATGGGCC	NP_001193984.1:p.Val693MetfsTer?
NM_001207056.2:c.1974_1975insATGGGCC	NP_001193985.1:p.Val659MetfsTer?
NM_006892.4:c.2451_2452insATGGGCC MANE Select	NP_008823.1:p.Val818MetfsTer?
NM_175848.2:c.2391_2392insATGGGCC	NP_787044.1:p.Val798MetfsTer?
NM_175849.2:c.2202_2203insATGGGCC	NP_787045.1:p.Val735MetfsTer?
NM_175850.3:c.2427_2428insATGGGCC	NP_787046.1:p.Val810MetfsTer?