Canonical Allele Identifier: CA305179966
Gene: DNMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10174102A>T , CM000681.2:g.10174102A>T GRCh38
NC_000019.9:g.10284778A>T , CM000681.1:g.10284778A>T GRCh37
NC_000019.8:g.10145778A>T NCBI36
NG_028016.3:g.62185T>A , LRG_362:g.62185T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.649-197T>A MANE Select ENSP00000352516.3:n.649-197T>A
ENST00000676604.1:n.255-197T>A
ENST00000676610.1:c.601-197T>A ENSP00000504236.1:n.601-197T>A
ENST00000676820.1:n.657-197T>A
ENST00000677013.1:c.*291-197T>A ENSP00000503135.1:n.*291-197T>A
ENST00000677250.1:c.601-197T>A ENSP00000502894.1:n.601-197T>A
ENST00000677616.1:c.286-197T>A ENSP00000503055.1:n.286-197T>A
ENST00000677634.1:c.601-197T>A ENSP00000504246.1:n.601-197T>A
ENST00000677685.1:c.381-197T>A ENSP00000503407.1:n.381-197T>A
ENST00000677946.1:c.601-197T>A ENSP00000504202.1:n.601-197T>A
ENST00000678024.1:n.738-197T>A
ENST00000678804.1:c.601-197T>A ENSP00000503853.1:n.601-197T>A
ENST00000679103.1:c.601-197T>A ENSP00000503151.1:n.601-197T>A
ENST00000679313.1:c.601-197T>A ENSP00000504512.1:n.601-197T>A
ENST00000340748.8:c.601-197T>A ENSP00000345739.3:n.601-197T>A
ENST00000359526.8:c.649-197T>A ENSP00000352516.3:n.649-197T>A
ENST00000540357.5:c.-408-197T>A ENSP00000440457.2:n.-408-197T>A
ENST00000586988.5:c.*429-197T>A ENSP00000464958.1:n.*429-197T>A
ENST00000588952.5:c.238-197T>A ENSP00000467050.1:n.238-197T>A
ENST00000592705.5:c.*339-197T>A ENSP00000466657.1:n.*339-197T>A
NM_001130823.1:c.649-197T>A , LRG_362t1:c.649-197T>A NP_001124295.1:n.649-197T>A
NM_001379.2:c.601-197T>A NP_001370.1:n.601-197T>A
XM_011527772.1:c.649-197T>A XP_011526074.1:n.649-197T>A
XM_011527773.1:c.601-197T>A XP_011526075.1:n.601-197T>A
XM_011527774.1:c.238-197T>A XP_011526076.1:n.238-197T>A
NM_001130823.2:c.649-197T>A NP_001124295.1:n.649-197T>A
NM_001318730.1:c.601-197T>A NP_001305659.1:n.601-197T>A
NM_001318731.1:c.286-197T>A NP_001305660.1:n.286-197T>A
NM_001379.3:c.601-197T>A NP_001370.1:n.601-197T>A
NM_001130823.3:c.649-197T>A MANE Select NP_001124295.1:n.649-197T>A
NM_001318730.2:c.601-197T>A NP_001305659.1:n.601-197T>A
NM_001318731.2:c.286-197T>A NP_001305660.1:n.286-197T>A
NM_001379.4:c.601-197T>A NP_001370.1:n.601-197T>A
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