Canonical Allele Identifier: CA2322289525

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154591T= , CM000681.2:g.10154591T=	GRCh38
NC_000019.9:g.10265267T= , CM000681.1:g.10265267T=	GRCh37
NC_000019.8:g.10126267T=	NCBI36
NG_028016.3:g.81696A= , LRG_362:g.81696A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1827A= MANE Select	ENSP00000352516.3:p.Gly609=
ENST00000676604.1:n.1439A=
ENST00000676610.1:c.1779A=	ENSP00000504236.1:p.Gly593=
ENST00000676820.1:n.1835A=
ENST00000676868.1:n.2463A=
ENST00000677013.1:c.*1469A=	ENSP00000503135.1:n.*1469A=
ENST00000677250.1:c.*899A=	ENSP00000502894.1:n.*899A=
ENST00000677616.1:c.1470A=	ENSP00000503055.1:p.Gly490=
ENST00000677634.1:c.1779A=	ENSP00000504246.1:p.Gly593=
ENST00000677685.1:c.*1004A=	ENSP00000503407.1:n.*1004A=
ENST00000677783.1:n.2249A=
ENST00000677946.1:c.1779A=	ENSP00000504202.1:p.Gly593=
ENST00000678024.1:n.1922A=
ENST00000678694.1:n.1100A=
ENST00000678804.1:c.1779A=	ENSP00000503853.1:p.Gly593=
ENST00000679103.1:c.1779A=	ENSP00000503151.1:p.Gly593=
ENST00000679313.1:c.1779A=	ENSP00000504512.1:p.Gly593=
ENST00000340748.8:c.1779A=	ENSP00000345739.3:p.Gly593=
ENST00000359526.8:c.1827A=	ENSP00000352516.3:p.Gly609=
ENST00000540357.5:c.771A=	ENSP00000440457.2:p.Gly257=
ENST00000586799.1:c.213A=
ENST00000592705.5:c.*1517A=	ENSP00000466657.1:n.*1517A=
NM_001130823.1:c.1827A= , LRG_362t1:c.1827A=	NP_001124295.1:p.Gly609=
NM_001379.2:c.1779A=	NP_001370.1:p.Gly593=
XM_011527772.1:c.1827A=	XP_011526074.1:p.Gly609=
XM_011527773.1:c.1779A=	XP_011526075.1:p.Gly593=
XM_011527774.1:c.1416A=	XP_011526076.1:p.Gly472=
NM_001130823.2:c.1827A=	NP_001124295.1:p.Gly609=
NM_001318730.1:c.1779A=	NP_001305659.1:p.Gly593=
NM_001318731.1:c.1464A=	NP_001305660.1:p.Gly488=
NM_001379.3:c.1779A=	NP_001370.1:p.Gly593=
NM_001130823.3:c.1827A= MANE Select	NP_001124295.1:p.Gly609=
NM_001318730.2:c.1779A=	NP_001305659.1:p.Gly593=
NM_001318731.2:c.1464A=	NP_001305660.1:p.Gly488=
NM_001379.4:c.1779A=	NP_001370.1:p.Gly593=