Canonical Allele Identifier: CA2322289523

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154587T= , CM000681.2:g.10154587T=	GRCh38
NC_000019.9:g.10265263T= , CM000681.1:g.10265263T=	GRCh37
NC_000019.8:g.10126263T=	NCBI36
NG_028016.3:g.81700A= , LRG_362:g.81700A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1831A= MANE Select	ENSP00000352516.3:p.Arg611=
ENST00000676604.1:n.1443A=
ENST00000676610.1:c.1783A=	ENSP00000504236.1:p.Arg595=
ENST00000676820.1:n.1839A=
ENST00000676868.1:n.2467A=
ENST00000677013.1:c.*1473A=	ENSP00000503135.1:n.*1473A=
ENST00000677250.1:c.*903A=	ENSP00000502894.1:n.*903A=
ENST00000677616.1:c.1474A=	ENSP00000503055.1:p.Arg492=
ENST00000677634.1:c.1783A=	ENSP00000504246.1:p.Arg595=
ENST00000677685.1:c.*1008A=	ENSP00000503407.1:n.*1008A=
ENST00000677783.1:n.2253A=
ENST00000677946.1:c.1783A=	ENSP00000504202.1:p.Arg595=
ENST00000678024.1:n.1926A=
ENST00000678694.1:n.1104A=
ENST00000678804.1:c.1783A=	ENSP00000503853.1:p.Arg595=
ENST00000679103.1:c.1783A=	ENSP00000503151.1:p.Arg595=
ENST00000679313.1:c.1783A=	ENSP00000504512.1:p.Arg595=
ENST00000340748.8:c.1783A=	ENSP00000345739.3:p.Arg595=
ENST00000359526.8:c.1831A=	ENSP00000352516.3:p.Arg611=
ENST00000540357.5:c.775A=	ENSP00000440457.2:p.Arg259=
ENST00000586799.1:c.217A=
ENST00000592705.5:c.*1521A=	ENSP00000466657.1:n.*1521A=
NM_001130823.1:c.1831A= , LRG_362t1:c.1831A=	NP_001124295.1:p.Arg611=
NM_001379.2:c.1783A=	NP_001370.1:p.Arg595=
XM_011527772.1:c.1831A=	XP_011526074.1:p.Arg611=
XM_011527773.1:c.1783A=	XP_011526075.1:p.Arg595=
XM_011527774.1:c.1420A=	XP_011526076.1:p.Arg474=
NM_001130823.2:c.1831A=	NP_001124295.1:p.Arg611=
NM_001318730.1:c.1783A=	NP_001305659.1:p.Arg595=
NM_001318731.1:c.1468A=	NP_001305660.1:p.Arg490=
NM_001379.3:c.1783A=	NP_001370.1:p.Arg595=
NM_001130823.3:c.1831A= MANE Select	NP_001124295.1:p.Arg611=
NM_001318730.2:c.1783A=	NP_001305659.1:p.Arg595=
NM_001318731.2:c.1468A=	NP_001305660.1:p.Arg490=
NM_001379.4:c.1783A=	NP_001370.1:p.Arg595=