Canonical Allele Identifier: CA2360465120

Gene: DNMT3B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.32805325_32805326delinsTG , CM000682.2:g.32805325_32805326delinsTG	GRCh38
NC_000020.10:g.31393131_31393132delinsTG , CM000682.1:g.31393131_31393132delinsTG	GRCh37
NC_000020.9:g.30856792_30856793delinsTG	NCBI36
NG_007290.1:g.47941_47942delinsTG , LRG_56:g.47941_47942delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696231.1:c.*1183-13_*1183-12delinsTG	ENSP00000512497.1:n.*1183-13_*1183-12delinsTG
ENST00000696232.1:c.2232-2437_2232-2436delinsTG	ENSP00000512498.1:n.2232-2437_2232-2436delinsTG
ENST00000696233.1:c.*975-2437_*975-2436delinsTG	ENSP00000512499.1:n.*975-2437_*975-2436delinsTG
ENST00000696238.1:c.*975-13_*975-12delinsTG	ENSP00000512502.1:n.*975-13_*975-12delinsTG
ENST00000696239.1:c.2013-13_2013-12delinsTG	ENSP00000512503.1:n.2013-13_2013-12delinsTG
ENST00000696245.1:n.327-884_327-883delinsTG
ENST00000201963.3:c.2208-13_2208-12delinsTG	ENSP00000201963.3:n.2208-13_2208-12delinsTG
ENST00000328111.6:c.2232-13_2232-12delinsTG MANE Select	ENSP00000328547.2:n.2232-13_2232-12delinsTG
ENST00000348286.6:c.2172-2437_2172-2436delinsTG	ENSP00000337764.2:n.2172-2437_2172-2436delinsTG
ENST00000353855.6:c.2172-13_2172-12delinsTG	ENSP00000313397.4:n.2172-13_2172-12delinsTG
ENST00000443239.7:c.2046-2437_2046-2436delinsTG	ENSP00000403169.2:n.2046-2437_2046-2436delinsTG
ENST00000456297.6:c.1944-2437_1944-2436delinsTG	ENSP00000412305.1:n.1944-2437_1944-2436delinsTG
NM_001207055.1:c.2046-2437_2046-2436delinsTG	NP_001193984.1:n.2046-2437_2046-2436delinsTG
NM_001207056.1:c.1944-2437_1944-2436delinsTG	NP_001193985.1:n.1944-2437_1944-2436delinsTG
NM_006892.3:c.2232-13_2232-12delinsTG , LRG_56t1:c.2232-13_2232-12delinsTG	NP_008823.1:n.2232-13_2232-12delinsTG
NM_175848.1:c.2172-13_2172-12delinsTG	NP_787044.1:n.2172-13_2172-12delinsTG
NM_175849.1:c.2172-2437_2172-2436delinsTG	NP_787045.1:n.2172-2437_2172-2436delinsTG
NM_175850.2:c.2208-13_2208-12delinsTG	NP_787046.1:n.2208-13_2208-12delinsTG
XM_011528653.1:c.2208-2437_2208-2436delinsTG	XP_011526955.1:n.2208-2437_2208-2436delinsTG
XM_011528654.1:c.2082-2437_2082-2436delinsTG	XP_011526956.1:n.2082-2437_2082-2436delinsTG
XR_936510.1:n.2199-13_2199-12delinsTG
XR_936511.1:n.2199-2437_2199-2436delinsTG
XR_936512.1:n.2074-13_2074-12delinsTG
XM_011528653.2:c.2208-2437_2208-2436delinsTG	XP_011526955.1:n.2208-2437_2208-2436delinsTG
XM_011528654.2:c.2082-2437_2082-2436delinsTG	XP_011526956.1:n.2082-2437_2082-2436delinsTG
XR_936510.2:n.2210-13_2210-12delinsTG
XR_936511.2:n.2210-2437_2210-2436delinsTG
XR_936512.2:n.2086-13_2086-12delinsTG
NM_001207055.2:c.2046-2437_2046-2436delinsTG	NP_001193984.1:n.2046-2437_2046-2436delinsTG
NM_001207056.2:c.1944-2437_1944-2436delinsTG	NP_001193985.1:n.1944-2437_1944-2436delinsTG
NM_006892.4:c.2232-13_2232-12delinsTG MANE Select	NP_008823.1:n.2232-13_2232-12delinsTG
NM_175848.2:c.2172-13_2172-12delinsTG	NP_787044.1:n.2172-13_2172-12delinsTG
NM_175849.2:c.2172-2437_2172-2436delinsTG	NP_787045.1:n.2172-2437_2172-2436delinsTG
NM_175850.3:c.2208-13_2208-12delinsTG	NP_787046.1:n.2208-13_2208-12delinsTG