Canonical Allele Identifier: CA2360466170
Gene: DNMT3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32807741_32807757delinsTTTTCACTCCGGTACCC , CM000682.2:g.32807741_32807757delinsTTTTCACTCCGGTACCC GRCh38
NC_000020.10:g.31395547_31395563delinsTTTTCACTCCGGTACCC , CM000682.1:g.31395547_31395563delinsTTTTCACTCCGGTACCC GRCh37
NC_000020.9:g.30859208_30859224delinsTTTTCACTCCGGTACCC NCBI36
NG_007290.1:g.50357_50373delinsTTTTCACTCCGGTACCC , LRG_56:g.50357_50373delinsTTTTCACTCCGGTACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000696231.1:c.*1372-21_*1372-5delinsTTTTCACTCCGGTACCC ENSP00000512497.1:n.*1372-21_*1372-5delinsTTTTCACTCCGGTACCC
ENST00000696232.1:c.2232-21_2232-5delinsTTTTCACTCCGGTACCC ENSP00000512498.1:n.2232-21_2232-5delinsTTTTCACTCCGGTACCC
ENST00000696233.1:c.*975-21_*975-5delinsTTTTCACTCCGGTACCC ENSP00000512499.1:n.*975-21_*975-5delinsTTTTCACTCCGGTACCC
ENST00000696238.1:c.*1164-21_*1164-5delinsTTTTCACTCCGGTACCC ENSP00000512502.1:n.*1164-21_*1164-5delinsTTTTCACTCCGGTACCC
ENST00000696239.1:c.2202-21_2202-5delinsTTTTCACTCCGGTACCC ENSP00000512503.1:n.2202-21_2202-5delinsTTTTCACTCCGGTACCC
ENST00000696245.1:n.446-21_446-5delinsTTTTCACTCCGGTACCC
ENST00000201963.3:c.2397-21_2397-5delinsTTTTCACTCCGGTACCC ENSP00000201963.3:n.2397-21_2397-5delinsTTTTCACTCCGGTACCC
ENST00000328111.6:c.2421-21_2421-5delinsTTTTCACTCCGGTACCC MANE Select ENSP00000328547.2:n.2421-21_2421-5delinsTTTTCACTCCGGTACCC
ENST00000348286.6:c.2172-21_2172-5delinsTTTTCACTCCGGTACCC ENSP00000337764.2:n.2172-21_2172-5delinsTTTTCACTCCGGTACCC
ENST00000353855.6:c.2361-21_2361-5delinsTTTTCACTCCGGTACCC ENSP00000313397.4:n.2361-21_2361-5delinsTTTTCACTCCGGTACCC
ENST00000443239.7:c.2046-21_2046-5delinsTTTTCACTCCGGTACCC ENSP00000403169.2:n.2046-21_2046-5delinsTTTTCACTCCGGTACCC
ENST00000456297.6:c.1944-21_1944-5delinsTTTTCACTCCGGTACCC ENSP00000412305.1:n.1944-21_1944-5delinsTTTTCACTCCGGTACCC
NM_001207055.1:c.2046-21_2046-5delinsTTTTCACTCCGGTACCC NP_001193984.1:n.2046-21_2046-5delinsTTTTCACTCCGGTACCC
NM_001207056.1:c.1944-21_1944-5delinsTTTTCACTCCGGTACCC NP_001193985.1:n.1944-21_1944-5delinsTTTTCACTCCGGTACCC
NM_006892.3:c.2421-21_2421-5delinsTTTTCACTCCGGTACCC , LRG_56t1:c.2421-21_2421-5delinsTTTTCACTCCGGTACCC NP_008823.1:n.2421-21_2421-5delinsTTTTCACTCCGGTACCC
NM_175848.1:c.2361-21_2361-5delinsTTTTCACTCCGGTACCC NP_787044.1:n.2361-21_2361-5delinsTTTTCACTCCGGTACCC
NM_175849.1:c.2172-21_2172-5delinsTTTTCACTCCGGTACCC NP_787045.1:n.2172-21_2172-5delinsTTTTCACTCCGGTACCC
NM_175850.2:c.2397-21_2397-5delinsTTTTCACTCCGGTACCC NP_787046.1:n.2397-21_2397-5delinsTTTTCACTCCGGTACCC
XM_011528653.1:c.2208-21_2208-5delinsTTTTCACTCCGGTACCC XP_011526955.1:n.2208-21_2208-5delinsTTTTCACTCCGGTACCC
XM_011528654.1:c.2082-21_2082-5delinsTTTTCACTCCGGTACCC XP_011526956.1:n.2082-21_2082-5delinsTTTTCACTCCGGTACCC
XR_936511.1:n.2199-21_2199-5delinsTTTTCACTCCGGTACCC
XM_011528653.2:c.2208-21_2208-5delinsTTTTCACTCCGGTACCC XP_011526955.1:n.2208-21_2208-5delinsTTTTCACTCCGGTACCC
XM_011528654.2:c.2082-21_2082-5delinsTTTTCACTCCGGTACCC XP_011526956.1:n.2082-21_2082-5delinsTTTTCACTCCGGTACCC
XR_936511.2:n.2210-21_2210-5delinsTTTTCACTCCGGTACCC
NM_001207055.2:c.2046-21_2046-5delinsTTTTCACTCCGGTACCC NP_001193984.1:n.2046-21_2046-5delinsTTTTCACTCCGGTACCC
NM_001207056.2:c.1944-21_1944-5delinsTTTTCACTCCGGTACCC NP_001193985.1:n.1944-21_1944-5delinsTTTTCACTCCGGTACCC
NM_006892.4:c.2421-21_2421-5delinsTTTTCACTCCGGTACCC MANE Select NP_008823.1:n.2421-21_2421-5delinsTTTTCACTCCGGTACCC
NM_175848.2:c.2361-21_2361-5delinsTTTTCACTCCGGTACCC NP_787044.1:n.2361-21_2361-5delinsTTTTCACTCCGGTACCC
NM_175849.2:c.2172-21_2172-5delinsTTTTCACTCCGGTACCC NP_787045.1:n.2172-21_2172-5delinsTTTTCACTCCGGTACCC
NM_175850.3:c.2397-21_2397-5delinsTTTTCACTCCGGTACCC NP_787046.1:n.2397-21_2397-5delinsTTTTCACTCCGGTACCC