Canonical Allele Identifier: CA403937966
Gene: DNMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10156404G>T , CM000681.2:g.10156404G>T GRCh38
NC_000019.9:g.10267080G>T , CM000681.1:g.10267080G>T GRCh37
NC_000019.8:g.10128080G>T NCBI36
NG_028016.3:g.79883C>A , LRG_362:g.79883C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1386C>A MANE Select ENSP00000352516.3:p.Asp462Glu
ENST00000676604.1:n.998C>A
ENST00000676610.1:c.1338C>A ENSP00000504236.1:p.Asp446Glu
ENST00000676820.1:n.1394C>A
ENST00000676868.1:n.2022C>A
ENST00000677013.1:c.*1028C>A ENSP00000503135.1:n.*1028C>A
ENST00000677250.1:c.*458C>A ENSP00000502894.1:n.*458C>A
ENST00000677616.1:c.1029C>A ENSP00000503055.1:p.Asp343Glu
ENST00000677634.1:c.1338C>A ENSP00000504246.1:p.Asp446Glu
ENST00000677685.1:c.*563C>A ENSP00000503407.1:n.*563C>A
ENST00000677783.1:n.1808C>A
ENST00000677946.1:c.1338C>A ENSP00000504202.1:p.Asp446Glu
ENST00000678024.1:n.1481C>A
ENST00000678694.1:n.659C>A
ENST00000678804.1:c.1338C>A ENSP00000503853.1:p.Asp446Glu
ENST00000679103.1:c.1338C>A ENSP00000503151.1:p.Asp446Glu
ENST00000679313.1:c.1338C>A ENSP00000504512.1:p.Asp446Glu
ENST00000340748.8:c.1338C>A ENSP00000345739.3:p.Asp446Glu
ENST00000359526.8:c.1386C>A ENSP00000352516.3:p.Asp462Glu
ENST00000540357.5:c.330C>A ENSP00000440457.2:p.Asp110Glu
ENST00000585843.1:n.543C>A
ENST00000592705.5:c.*1076C>A ENSP00000466657.1:n.*1076C>A
NM_001130823.1:c.1386C>A , LRG_362t1:c.1386C>A NP_001124295.1:p.Asp462Glu
NM_001379.2:c.1338C>A NP_001370.1:p.Asp446Glu
XM_011527772.1:c.1386C>A XP_011526074.1:p.Asp462Glu
XM_011527773.1:c.1338C>A XP_011526075.1:p.Asp446Glu
XM_011527774.1:c.975C>A XP_011526076.1:p.Asp325Glu
NM_001130823.2:c.1386C>A NP_001124295.1:p.Asp462Glu
NM_001318730.1:c.1338C>A NP_001305659.1:p.Asp446Glu
NM_001318731.1:c.1023C>A NP_001305660.1:p.Asp341Glu
NM_001379.3:c.1338C>A NP_001370.1:p.Asp446Glu
NM_001130823.3:c.1386C>A MANE Select NP_001124295.1:p.Asp462Glu
NM_001318730.2:c.1338C>A NP_001305659.1:p.Asp446Glu
NM_001318731.2:c.1023C>A NP_001305660.1:p.Asp341Glu
NM_001379.4:c.1338C>A NP_001370.1:p.Asp446Glu