Canonical Allele Identifier: CA403938328
Gene: DNMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10156494G>C , CM000681.2:g.10156494G>C GRCh38
NC_000019.9:g.10267170G>C , CM000681.1:g.10267170G>C GRCh37
NC_000019.8:g.10128170G>C NCBI36
NG_028016.3:g.79793C>G , LRG_362:g.79793C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1296C>G MANE Select ENSP00000352516.3:p.His432Gln
ENST00000676604.1:n.908C>G
ENST00000676610.1:c.1248C>G ENSP00000504236.1:p.His416Gln
ENST00000676820.1:n.1304C>G
ENST00000676868.1:n.1932C>G
ENST00000677013.1:c.*938C>G ENSP00000503135.1:n.*938C>G
ENST00000677250.1:c.*368C>G ENSP00000502894.1:n.*368C>G
ENST00000677616.1:c.939C>G ENSP00000503055.1:p.His313Gln
ENST00000677634.1:c.1248C>G ENSP00000504246.1:p.His416Gln
ENST00000677685.1:c.*473C>G ENSP00000503407.1:n.*473C>G
ENST00000677783.1:n.1718C>G
ENST00000677946.1:c.1248C>G ENSP00000504202.1:p.His416Gln
ENST00000678024.1:n.1391C>G
ENST00000678694.1:n.569C>G
ENST00000678804.1:c.1248C>G ENSP00000503853.1:p.His416Gln
ENST00000679103.1:c.1248C>G ENSP00000503151.1:p.His416Gln
ENST00000679313.1:c.1248C>G ENSP00000504512.1:p.His416Gln
ENST00000340748.8:c.1248C>G ENSP00000345739.3:p.His416Gln
ENST00000359526.8:c.1296C>G ENSP00000352516.3:p.His432Gln
ENST00000540357.5:c.240C>G ENSP00000440457.2:p.His80Gln
ENST00000585843.1:n.453C>G
ENST00000592705.5:c.*986C>G ENSP00000466657.1:n.*986C>G
NM_001130823.1:c.1296C>G , LRG_362t1:c.1296C>G NP_001124295.1:p.His432Gln
NM_001379.2:c.1248C>G NP_001370.1:p.His416Gln
XM_011527772.1:c.1296C>G XP_011526074.1:p.His432Gln
XM_011527773.1:c.1248C>G XP_011526075.1:p.His416Gln
XM_011527774.1:c.885C>G XP_011526076.1:p.His295Gln
NM_001130823.2:c.1296C>G NP_001124295.1:p.His432Gln
NM_001318730.1:c.1248C>G NP_001305659.1:p.His416Gln
NM_001318731.1:c.933C>G NP_001305660.1:p.His311Gln
NM_001379.3:c.1248C>G NP_001370.1:p.His416Gln
NM_001130823.3:c.1296C>G MANE Select NP_001124295.1:p.His432Gln
NM_001318730.2:c.1248C>G NP_001305659.1:p.His416Gln
NM_001318731.2:c.933C>G NP_001305660.1:p.His311Gln
NM_001379.4:c.1248C>G NP_001370.1:p.His416Gln