Canonical Allele Identifier: CA403929831

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149926C>T , CM000681.2:g.10149926C>T	GRCh38
NC_000019.9:g.10260602C>T , CM000681.1:g.10260602C>T	GRCh37
NC_000019.8:g.10121602C>T	NCBI36
NG_028016.3:g.86361G>A , LRG_362:g.86361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2308G>A MANE Select	ENSP00000352516.3:p.Ala770Thr
ENST00000586667.2:n.343G>A
ENST00000676604.1:n.1920G>A
ENST00000676610.1:c.2260G>A	ENSP00000504236.1:p.Ala754Thr
ENST00000676820.1:n.2316G>A
ENST00000676868.1:n.2944G>A
ENST00000677013.1:c.*1950G>A	ENSP00000503135.1:n.*1950G>A
ENST00000677250.1:c.*1380G>A	ENSP00000502894.1:n.*1380G>A
ENST00000677616.1:c.1951G>A	ENSP00000503055.1:p.Ala651Thr
ENST00000677634.1:c.2260G>A	ENSP00000504246.1:p.Ala754Thr
ENST00000677685.1:c.*1485G>A	ENSP00000503407.1:n.*1485G>A
ENST00000677783.1:n.2730G>A
ENST00000677946.1:c.2260G>A	ENSP00000504202.1:p.Ala754Thr
ENST00000678024.1:n.2403G>A
ENST00000678647.1:n.393G>A
ENST00000678694.1:n.1581G>A
ENST00000678804.1:c.2260G>A	ENSP00000503853.1:p.Ala754Thr
ENST00000679100.1:n.447G>A
ENST00000679103.1:c.2260G>A	ENSP00000503151.1:p.Ala754Thr
ENST00000679313.1:c.2260G>A	ENSP00000504512.1:p.Ala754Thr
ENST00000340748.8:c.2260G>A	ENSP00000345739.3:p.Ala754Thr
ENST00000359526.8:c.2308G>A	ENSP00000352516.3:p.Ala770Thr
ENST00000540357.5:c.1252G>A	ENSP00000440457.2:p.Ala418Thr
ENST00000586667.1:n.343G>A
ENST00000592705.5:c.*1998G>A	ENSP00000466657.1:n.*1998G>A
NM_001130823.1:c.2308G>A , LRG_362t1:c.2308G>A	NP_001124295.1:p.Ala770Thr
NM_001379.2:c.2260G>A	NP_001370.1:p.Ala754Thr
XM_011527772.1:c.2308G>A	XP_011526074.1:p.Ala770Thr
XM_011527773.1:c.2260G>A	XP_011526075.1:p.Ala754Thr
XM_011527774.1:c.1897G>A	XP_011526076.1:p.Ala633Thr
NM_001130823.2:c.2308G>A	NP_001124295.1:p.Ala770Thr
NM_001318730.1:c.2260G>A	NP_001305659.1:p.Ala754Thr
NM_001318731.1:c.1945G>A	NP_001305660.1:p.Ala649Thr
NM_001379.3:c.2260G>A	NP_001370.1:p.Ala754Thr
NM_001130823.3:c.2308G>A MANE Select	NP_001124295.1:p.Ala770Thr
NM_001318730.2:c.2260G>A	NP_001305659.1:p.Ala754Thr
NM_001318731.2:c.1945G>A	NP_001305660.1:p.Ala649Thr
NM_001379.4:c.2260G>A	NP_001370.1:p.Ala754Thr