Canonical Allele Identifier: CA505467443
Gene: DNMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10265291G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10154615G>T , CM000681.2:g.10154615G>T GRCh38
NC_000019.9:g.10265291G>T , CM000681.1:g.10265291G>T GRCh37
NC_000019.8:g.10126291G>T NCBI36
NG_028016.3:g.81672C>A , LRG_362:g.81672C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1803C>A MANE Select ENSP00000352516.3:p.Ile601=
ENST00000676604.1:n.1415C>A
ENST00000676610.1:c.1755C>A ENSP00000504236.1:p.Ile585=
ENST00000676820.1:n.1811C>A
ENST00000676868.1:n.2439C>A
ENST00000677013.1:c.*1445C>A ENSP00000503135.1:n.*1445C>A
ENST00000677250.1:c.*875C>A ENSP00000502894.1:n.*875C>A
ENST00000677616.1:c.1446C>A ENSP00000503055.1:p.Ile482=
ENST00000677634.1:c.1755C>A ENSP00000504246.1:p.Ile585=
ENST00000677685.1:c.*980C>A ENSP00000503407.1:n.*980C>A
ENST00000677783.1:n.2225C>A
ENST00000677946.1:c.1755C>A ENSP00000504202.1:p.Ile585=
ENST00000678024.1:n.1898C>A
ENST00000678694.1:n.1076C>A
ENST00000678804.1:c.1755C>A ENSP00000503853.1:p.Ile585=
ENST00000679103.1:c.1755C>A ENSP00000503151.1:p.Ile585=
ENST00000679313.1:c.1755C>A ENSP00000504512.1:p.Ile585=
ENST00000340748.8:c.1755C>A ENSP00000345739.3:p.Ile585=
ENST00000359526.8:c.1803C>A ENSP00000352516.3:p.Ile601=
ENST00000540357.5:c.747C>A ENSP00000440457.2:p.Ile249=
ENST00000586799.1:c.189C>A
ENST00000592705.5:c.*1493C>A ENSP00000466657.1:n.*1493C>A
NM_001130823.1:c.1803C>A , LRG_362t1:c.1803C>A NP_001124295.1:p.Ile601=
NM_001379.2:c.1755C>A NP_001370.1:p.Ile585=
XM_011527772.1:c.1803C>A XP_011526074.1:p.Ile601=
XM_011527773.1:c.1755C>A XP_011526075.1:p.Ile585=
XM_011527774.1:c.1392C>A XP_011526076.1:p.Ile464=
NM_001130823.2:c.1803C>A NP_001124295.1:p.Ile601=
NM_001318730.1:c.1755C>A NP_001305659.1:p.Ile585=
NM_001318731.1:c.1440C>A NP_001305660.1:p.Ile480=
NM_001379.3:c.1755C>A NP_001370.1:p.Ile585=
NM_001130823.3:c.1803C>A MANE Select NP_001124295.1:p.Ile601=
NM_001318730.2:c.1755C>A NP_001305659.1:p.Ile585=
NM_001318731.2:c.1440C>A NP_001305660.1:p.Ile480=
NM_001379.4:c.1755C>A NP_001370.1:p.Ile585=