Canonical Allele Identifier: CA2322287382

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149924C= , CM000681.2:g.10149924C=	GRCh38
NC_000019.9:g.10260600C= , CM000681.1:g.10260600C=	GRCh37
NC_000019.8:g.10121600C=	NCBI36
NG_028016.3:g.86363G= , LRG_362:g.86363G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2310G= MANE Select	ENSP00000352516.3:p.Ala770=
ENST00000586667.2:n.345G=
ENST00000676604.1:n.1922G=
ENST00000676610.1:c.2262G=	ENSP00000504236.1:p.Ala754=
ENST00000676820.1:n.2318G=
ENST00000676868.1:n.2946G=
ENST00000677013.1:c.*1952G=	ENSP00000503135.1:n.*1952G=
ENST00000677250.1:c.*1382G=	ENSP00000502894.1:n.*1382G=
ENST00000677616.1:c.1953G=	ENSP00000503055.1:p.Ala651=
ENST00000677634.1:c.2262G=	ENSP00000504246.1:p.Ala754=
ENST00000677685.1:c.*1487G=	ENSP00000503407.1:n.*1487G=
ENST00000677783.1:n.2732G=
ENST00000677946.1:c.2262G=	ENSP00000504202.1:p.Ala754=
ENST00000678024.1:n.2405G=
ENST00000678647.1:n.395G=
ENST00000678694.1:n.1583G=
ENST00000678804.1:c.2262G=	ENSP00000503853.1:p.Ala754=
ENST00000679100.1:n.449G=
ENST00000679103.1:c.2262G=	ENSP00000503151.1:p.Ala754=
ENST00000679313.1:c.2262G=	ENSP00000504512.1:p.Ala754=
ENST00000340748.8:c.2262G=	ENSP00000345739.3:p.Ala754=
ENST00000359526.8:c.2310G=	ENSP00000352516.3:p.Ala770=
ENST00000540357.5:c.1254G=	ENSP00000440457.2:p.Ala418=
ENST00000586667.1:n.345G=
ENST00000592705.5:c.*2000G=	ENSP00000466657.1:n.*2000G=
NM_001130823.1:c.2310G= , LRG_362t1:c.2310G=	NP_001124295.1:p.Ala770=
NM_001379.2:c.2262G=	NP_001370.1:p.Ala754=
XM_011527772.1:c.2310G=	XP_011526074.1:p.Ala770=
XM_011527773.1:c.2262G=	XP_011526075.1:p.Ala754=
XM_011527774.1:c.1899G=	XP_011526076.1:p.Ala633=
NM_001130823.2:c.2310G=	NP_001124295.1:p.Ala770=
NM_001318730.1:c.2262G=	NP_001305659.1:p.Ala754=
NM_001318731.1:c.1947G=	NP_001305660.1:p.Ala649=
NM_001379.3:c.2262G=	NP_001370.1:p.Ala754=
NM_001130823.3:c.2310G= MANE Select	NP_001124295.1:p.Ala770=
NM_001318730.2:c.2262G=	NP_001305659.1:p.Ala754=
NM_001318731.2:c.1947G=	NP_001305660.1:p.Ala649=
NM_001379.4:c.2262G=	NP_001370.1:p.Ala754=