Canonical Allele Identifier: CA403929843

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149929C>A , CM000681.2:g.10149929C>A	GRCh38
NC_000019.9:g.10260605C>A , CM000681.1:g.10260605C>A	GRCh37
NC_000019.8:g.10121605C>A	NCBI36
NG_028016.3:g.86358G>T , LRG_362:g.86358G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2305G>T MANE Select	ENSP00000352516.3:p.Asp769Tyr
ENST00000586667.2:n.340G>T
ENST00000676604.1:n.1917G>T
ENST00000676610.1:c.2257G>T	ENSP00000504236.1:p.Asp753Tyr
ENST00000676820.1:n.2313G>T
ENST00000676868.1:n.2941G>T
ENST00000677013.1:c.*1947G>T	ENSP00000503135.1:n.*1947G>T
ENST00000677250.1:c.*1377G>T	ENSP00000502894.1:n.*1377G>T
ENST00000677616.1:c.1948G>T	ENSP00000503055.1:p.Asp650Tyr
ENST00000677634.1:c.2257G>T	ENSP00000504246.1:p.Asp753Tyr
ENST00000677685.1:c.*1482G>T	ENSP00000503407.1:n.*1482G>T
ENST00000677783.1:n.2727G>T
ENST00000677946.1:c.2257G>T	ENSP00000504202.1:p.Asp753Tyr
ENST00000678024.1:n.2400G>T
ENST00000678647.1:n.390G>T
ENST00000678694.1:n.1578G>T
ENST00000678804.1:c.2257G>T	ENSP00000503853.1:p.Asp753Tyr
ENST00000679100.1:n.444G>T
ENST00000679103.1:c.2257G>T	ENSP00000503151.1:p.Asp753Tyr
ENST00000679313.1:c.2257G>T	ENSP00000504512.1:p.Asp753Tyr
ENST00000340748.8:c.2257G>T	ENSP00000345739.3:p.Asp753Tyr
ENST00000359526.8:c.2305G>T	ENSP00000352516.3:p.Asp769Tyr
ENST00000540357.5:c.1249G>T	ENSP00000440457.2:p.Asp417Tyr
ENST00000586667.1:n.340G>T
ENST00000592705.5:c.*1995G>T	ENSP00000466657.1:n.*1995G>T
NM_001130823.1:c.2305G>T , LRG_362t1:c.2305G>T	NP_001124295.1:p.Asp769Tyr
NM_001379.2:c.2257G>T	NP_001370.1:p.Asp753Tyr
XM_011527772.1:c.2305G>T	XP_011526074.1:p.Asp769Tyr
XM_011527773.1:c.2257G>T	XP_011526075.1:p.Asp753Tyr
XM_011527774.1:c.1894G>T	XP_011526076.1:p.Asp632Tyr
NM_001130823.2:c.2305G>T	NP_001124295.1:p.Asp769Tyr
NM_001318730.1:c.2257G>T	NP_001305659.1:p.Asp753Tyr
NM_001318731.1:c.1942G>T	NP_001305660.1:p.Asp648Tyr
NM_001379.3:c.2257G>T	NP_001370.1:p.Asp753Tyr
NM_001130823.3:c.2305G>T MANE Select	NP_001124295.1:p.Asp769Tyr
NM_001318730.2:c.2257G>T	NP_001305659.1:p.Asp753Tyr
NM_001318731.2:c.1942G>T	NP_001305660.1:p.Asp648Tyr
NM_001379.4:c.2257G>T	NP_001370.1:p.Asp753Tyr