Canonical Allele Identifier: CA9187485

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10136274G>A , CM000681.2:g.10136274G>A	GRCh38
NC_000019.9:g.10246950G>A , CM000681.1:g.10246950G>A	GRCh37
NC_000019.8:g.10107950G>A	NCBI36
NG_028016.3:g.100013C>T , LRG_362:g.100013C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.4503C>T MANE Select	ENSP00000352516.3:p.Cys1501=
ENST00000586667.2:n.2538C>T
ENST00000589351.6:n.3689C>T
ENST00000676604.1:n.4115C>T
ENST00000676610.1:c.4455C>T	ENSP00000504236.1:p.Cys1485=
ENST00000676820.1:n.5349C>T
ENST00000676868.1:n.5139C>T
ENST00000677013.1:c.*4145C>T	ENSP00000503135.1:n.*4145C>T
ENST00000677038.1:n.1051C>T
ENST00000677250.1:c.*3575C>T	ENSP00000502894.1:n.*3575C>T
ENST00000677616.1:c.*725C>T	ENSP00000503055.1:n.*725C>T
ENST00000677634.1:c.*1058C>T	ENSP00000504246.1:n.*1058C>T
ENST00000677685.1:c.*3680C>T	ENSP00000503407.1:n.*3680C>T
ENST00000677783.1:n.5763C>T
ENST00000677946.1:c.4455C>T	ENSP00000504202.1:p.Cys1485=
ENST00000678024.1:n.5436C>T
ENST00000678107.1:n.1498C>T
ENST00000678239.1:n.1356C>T
ENST00000678647.1:n.2597C>T
ENST00000678694.1:n.3776C>T
ENST00000678804.1:c.4464C>T	ENSP00000503853.1:p.Cys1488=
ENST00000678851.1:n.497C>T
ENST00000678957.1:n.2167C>T
ENST00000679100.1:n.2642C>T
ENST00000679103.1:c.4455C>T	ENSP00000503151.1:p.Cys1485=
ENST00000679313.1:c.4464C>T	ENSP00000504512.1:p.Cys1488=
ENST00000340748.8:c.4455C>T	ENSP00000345739.3:p.Cys1485=
ENST00000359526.8:c.4503C>T	ENSP00000352516.3:p.Cys1501=
ENST00000540357.5:c.3447C>T	ENSP00000440457.2:p.Cys1149=
ENST00000586588.5:n.2376C>T
ENST00000588913.5:c.782C>T
ENST00000592705.5:c.*4193C>T	ENSP00000466657.1:n.*4193C>T
NM_001130823.1:c.4503C>T , LRG_362t1:c.4503C>T	NP_001124295.1:p.Cys1501=
NM_001379.2:c.4455C>T	NP_001370.1:p.Cys1485=
XM_011527772.1:c.4512C>T	XP_011526074.1:p.Cys1504=
XM_011527773.1:c.4464C>T	XP_011526075.1:p.Cys1488=
XM_011527774.1:c.4101C>T	XP_011526076.1:p.Cys1367=
NM_001130823.2:c.4503C>T	NP_001124295.1:p.Cys1501=
NM_001318730.1:c.4464C>T	NP_001305659.1:p.Cys1488=
NM_001318731.1:c.4140C>T	NP_001305660.1:p.Cys1380=
NM_001379.3:c.4455C>T	NP_001370.1:p.Cys1485=
NM_001130823.3:c.4503C>T MANE Select	NP_001124295.1:p.Cys1501=
NM_001318730.2:c.4464C>T	NP_001305659.1:p.Cys1488=
NM_001318731.2:c.4140C>T	NP_001305660.1:p.Cys1380=
NM_001379.4:c.4455C>T	NP_001370.1:p.Cys1485=