Canonical Allele Identifier: CA2322287380

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149919G= , CM000681.2:g.10149919G=	GRCh38
NC_000019.9:g.10260595G= , CM000681.1:g.10260595G=	GRCh37
NC_000019.8:g.10121595G=	NCBI36
NG_028016.3:g.86368C= , LRG_362:g.86368C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2315C= MANE Select	ENSP00000352516.3:p.Thr772=
ENST00000586667.2:n.350C=
ENST00000676604.1:n.1927C=
ENST00000676610.1:c.2267C=	ENSP00000504236.1:p.Thr756=
ENST00000676820.1:n.2323C=
ENST00000676868.1:n.2951C=
ENST00000677013.1:c.*1957C=	ENSP00000503135.1:n.*1957C=
ENST00000677250.1:c.*1387C=	ENSP00000502894.1:n.*1387C=
ENST00000677616.1:c.1958C=	ENSP00000503055.1:p.Thr653=
ENST00000677634.1:c.2267C=	ENSP00000504246.1:p.Thr756=
ENST00000677685.1:c.*1492C=	ENSP00000503407.1:n.*1492C=
ENST00000677783.1:n.2737C=
ENST00000677946.1:c.2267C=	ENSP00000504202.1:p.Thr756=
ENST00000678024.1:n.2410C=
ENST00000678647.1:n.400C=
ENST00000678694.1:n.1588C=
ENST00000678804.1:c.2267C=	ENSP00000503853.1:p.Thr756=
ENST00000679100.1:n.454C=
ENST00000679103.1:c.2267C=	ENSP00000503151.1:p.Thr756=
ENST00000679313.1:c.2267C=	ENSP00000504512.1:p.Thr756=
ENST00000340748.8:c.2267C=	ENSP00000345739.3:p.Thr756=
ENST00000359526.8:c.2315C=	ENSP00000352516.3:p.Thr772=
ENST00000540357.5:c.1259C=	ENSP00000440457.2:p.Thr420=
ENST00000586667.1:n.350C=
ENST00000592705.5:c.*2005C=	ENSP00000466657.1:n.*2005C=
NM_001130823.1:c.2315C= , LRG_362t1:c.2315C=	NP_001124295.1:p.Thr772=
NM_001379.2:c.2267C=	NP_001370.1:p.Thr756=
XM_011527772.1:c.2315C=	XP_011526074.1:p.Thr772=
XM_011527773.1:c.2267C=	XP_011526075.1:p.Thr756=
XM_011527774.1:c.1904C=	XP_011526076.1:p.Thr635=
NM_001130823.2:c.2315C=	NP_001124295.1:p.Thr772=
NM_001318730.1:c.2267C=	NP_001305659.1:p.Thr756=
NM_001318731.1:c.1952C=	NP_001305660.1:p.Thr651=
NM_001379.3:c.2267C=	NP_001370.1:p.Thr756=
NM_001130823.3:c.2315C= MANE Select	NP_001124295.1:p.Thr772=
NM_001318730.2:c.2267C=	NP_001305659.1:p.Thr756=
NM_001318731.2:c.1952C=	NP_001305660.1:p.Thr651=
NM_001379.4:c.2267C=	NP_001370.1:p.Thr756=