Canonical Allele Identifier: CA403929806

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149920T>C , CM000681.2:g.10149920T>C	GRCh38
NC_000019.9:g.10260596T>C , CM000681.1:g.10260596T>C	GRCh37
NC_000019.8:g.10121596T>C	NCBI36
NG_028016.3:g.86367A>G , LRG_362:g.86367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2314A>G MANE Select	ENSP00000352516.3:p.Thr772Ala
ENST00000586667.2:n.349A>G
ENST00000676604.1:n.1926A>G
ENST00000676610.1:c.2266A>G	ENSP00000504236.1:p.Thr756Ala
ENST00000676820.1:n.2322A>G
ENST00000676868.1:n.2950A>G
ENST00000677013.1:c.*1956A>G	ENSP00000503135.1:n.*1956A>G
ENST00000677250.1:c.*1386A>G	ENSP00000502894.1:n.*1386A>G
ENST00000677616.1:c.1957A>G	ENSP00000503055.1:p.Thr653Ala
ENST00000677634.1:c.2266A>G	ENSP00000504246.1:p.Thr756Ala
ENST00000677685.1:c.*1491A>G	ENSP00000503407.1:n.*1491A>G
ENST00000677783.1:n.2736A>G
ENST00000677946.1:c.2266A>G	ENSP00000504202.1:p.Thr756Ala
ENST00000678024.1:n.2409A>G
ENST00000678647.1:n.399A>G
ENST00000678694.1:n.1587A>G
ENST00000678804.1:c.2266A>G	ENSP00000503853.1:p.Thr756Ala
ENST00000679100.1:n.453A>G
ENST00000679103.1:c.2266A>G	ENSP00000503151.1:p.Thr756Ala
ENST00000679313.1:c.2266A>G	ENSP00000504512.1:p.Thr756Ala
ENST00000340748.8:c.2266A>G	ENSP00000345739.3:p.Thr756Ala
ENST00000359526.8:c.2314A>G	ENSP00000352516.3:p.Thr772Ala
ENST00000540357.5:c.1258A>G	ENSP00000440457.2:p.Thr420Ala
ENST00000586667.1:n.349A>G
ENST00000592705.5:c.*2004A>G	ENSP00000466657.1:n.*2004A>G
NM_001130823.1:c.2314A>G , LRG_362t1:c.2314A>G	NP_001124295.1:p.Thr772Ala
NM_001379.2:c.2266A>G	NP_001370.1:p.Thr756Ala
XM_011527772.1:c.2314A>G	XP_011526074.1:p.Thr772Ala
XM_011527773.1:c.2266A>G	XP_011526075.1:p.Thr756Ala
XM_011527774.1:c.1903A>G	XP_011526076.1:p.Thr635Ala
NM_001130823.2:c.2314A>G	NP_001124295.1:p.Thr772Ala
NM_001318730.1:c.2266A>G	NP_001305659.1:p.Thr756Ala
NM_001318731.1:c.1951A>G	NP_001305660.1:p.Thr651Ala
NM_001379.3:c.2266A>G	NP_001370.1:p.Thr756Ala
NM_001130823.3:c.2314A>G MANE Select	NP_001124295.1:p.Thr772Ala
NM_001318730.2:c.2266A>G	NP_001305659.1:p.Thr756Ala
NM_001318731.2:c.1951A>G	NP_001305660.1:p.Thr651Ala
NM_001379.4:c.2266A>G	NP_001370.1:p.Thr756Ala