Canonical Allele Identifier: CA9187360

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10133690C>T , CM000681.2:g.10133690C>T	GRCh38
NC_000019.9:g.10244366C>T , CM000681.1:g.10244366C>T	GRCh37
NC_000019.8:g.10105366C>T	NCBI36
NG_028016.3:g.102597G>A , LRG_362:g.102597G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.4876G>A MANE Select	ENSP00000352516.3:p.Glu1626Lys
ENST00000586667.2:n.2911G>A
ENST00000589351.6:n.4062G>A
ENST00000676604.1:n.4488G>A
ENST00000676610.1:c.*1929G>A	ENSP00000504236.1:n.*1929G>A
ENST00000676820.1:n.5722G>A
ENST00000676868.1:n.5512G>A
ENST00000677013.1:c.*4518G>A	ENSP00000503135.1:n.*4518G>A
ENST00000677038.1:n.1424G>A
ENST00000677135.1:n.357G>A
ENST00000677250.1:c.*3948G>A	ENSP00000502894.1:n.*3948G>A
ENST00000677616.1:c.*1098G>A	ENSP00000503055.1:n.*1098G>A
ENST00000677634.1:c.*1431G>A	ENSP00000504246.1:n.*1431G>A
ENST00000677685.1:c.*4053G>A	ENSP00000503407.1:n.*4053G>A
ENST00000677783.1:n.6136G>A
ENST00000677946.1:c.*375G>A	ENSP00000504202.1:n.*375G>A
ENST00000678024.1:n.5809G>A
ENST00000678107.1:n.1871G>A
ENST00000678647.1:n.2970G>A
ENST00000678694.1:n.4149G>A
ENST00000678804.1:c.*375G>A	ENSP00000503853.1:n.*375G>A
ENST00000678851.1:n.2813G>A
ENST00000678957.1:n.2540G>A
ENST00000679100.1:n.3015G>A
ENST00000679103.1:c.*3G>A	ENSP00000503151.1:n.*3G>A
ENST00000679313.1:c.*3G>A	ENSP00000504512.1:n.*3G>A
ENST00000340748.8:c.4828G>A	ENSP00000345739.3:p.Glu1610Lys
ENST00000359526.8:c.4876G>A	ENSP00000352516.3:p.Glu1626Lys
ENST00000540357.5:c.3820G>A	ENSP00000440457.2:p.Glu1274Lys
ENST00000586588.5:n.2749G>A
ENST00000588913.5:c.1452G>A
ENST00000591798.5:n.182G>A
ENST00000592705.5:c.*4566G>A	ENSP00000466657.1:n.*4566G>A
NM_001130823.1:c.4876G>A , LRG_362t1:c.4876G>A	NP_001124295.1:p.Glu1626Lys
NM_001379.2:c.4828G>A	NP_001370.1:p.Glu1610Lys
XM_011527772.1:c.4885G>A	XP_011526074.1:p.Glu1629Lys
XM_011527773.1:c.4837G>A	XP_011526075.1:p.Glu1613Lys
XM_011527774.1:c.4474G>A	XP_011526076.1:p.Glu1492Lys
NM_001130823.2:c.4876G>A	NP_001124295.1:p.Glu1626Lys
NM_001318730.1:c.4837G>A	NP_001305659.1:p.Glu1613Lys
NM_001318731.1:c.4513G>A	NP_001305660.1:p.Glu1505Lys
NM_001379.3:c.4828G>A	NP_001370.1:p.Glu1610Lys
NM_001130823.3:c.4876G>A MANE Select	NP_001124295.1:p.Glu1626Lys
NM_001318730.2:c.4837G>A	NP_001305659.1:p.Glu1613Lys
NM_001318731.2:c.4513G>A	NP_001305660.1:p.Glu1505Lys
NM_001379.4:c.4828G>A	NP_001370.1:p.Glu1610Lys