Canonical Allele Identifier: CA2813560749
Gene: DNMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10156538C>G , CM000681.2:g.10156538C>G GRCh38
NC_000019.9:g.10267214C>G , CM000681.1:g.10267214C>G GRCh37
NC_000019.8:g.10128214C>G NCBI36
NG_028016.3:g.79749G>C , LRG_362:g.79749G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1281-29G>C MANE Select ENSP00000352516.3:n.1281-29G>C
ENST00000676604.1:n.893-29G>C
ENST00000676610.1:c.1233-29G>C ENSP00000504236.1:n.1233-29G>C
ENST00000676820.1:n.1289-29G>C
ENST00000676868.1:n.1917-29G>C
ENST00000677013.1:c.*923-29G>C ENSP00000503135.1:n.*923-29G>C
ENST00000677250.1:c.*353-29G>C ENSP00000502894.1:n.*353-29G>C
ENST00000677616.1:c.924-29G>C ENSP00000503055.1:n.924-29G>C
ENST00000677634.1:c.1233-29G>C ENSP00000504246.1:n.1233-29G>C
ENST00000677685.1:c.*458-29G>C ENSP00000503407.1:n.*458-29G>C
ENST00000677783.1:n.1703-29G>C
ENST00000677946.1:c.1233-29G>C ENSP00000504202.1:n.1233-29G>C
ENST00000678024.1:n.1376-29G>C
ENST00000678694.1:n.554-29G>C
ENST00000678804.1:c.1233-29G>C ENSP00000503853.1:n.1233-29G>C
ENST00000679103.1:c.1233-29G>C ENSP00000503151.1:n.1233-29G>C
ENST00000679313.1:c.1233-29G>C ENSP00000504512.1:n.1233-29G>C
ENST00000340748.8:c.1233-29G>C ENSP00000345739.3:n.1233-29G>C
ENST00000359526.8:c.1281-29G>C ENSP00000352516.3:n.1281-29G>C
ENST00000540357.5:c.225-29G>C ENSP00000440457.2:n.225-29G>C
ENST00000585843.1:n.438-29G>C
ENST00000592705.5:c.*971-29G>C ENSP00000466657.1:n.*971-29G>C
NM_001130823.1:c.1281-29G>C , LRG_362t1:c.1281-29G>C NP_001124295.1:n.1281-29G>C
NM_001379.2:c.1233-29G>C NP_001370.1:n.1233-29G>C
XM_011527772.1:c.1281-29G>C XP_011526074.1:n.1281-29G>C
XM_011527773.1:c.1233-29G>C XP_011526075.1:n.1233-29G>C
XM_011527774.1:c.870-29G>C XP_011526076.1:n.870-29G>C
NM_001130823.2:c.1281-29G>C NP_001124295.1:n.1281-29G>C
NM_001318730.1:c.1233-29G>C NP_001305659.1:n.1233-29G>C
NM_001318731.1:c.918-29G>C NP_001305660.1:n.918-29G>C
NM_001379.3:c.1233-29G>C NP_001370.1:n.1233-29G>C
NM_001130823.3:c.1281-29G>C MANE Select NP_001124295.1:n.1281-29G>C
NM_001318730.2:c.1233-29G>C NP_001305659.1:n.1233-29G>C
NM_001318731.2:c.918-29G>C NP_001305660.1:n.918-29G>C
NM_001379.4:c.1233-29G>C NP_001370.1:n.1233-29G>C