Canonical Allele Identifier: CA403929838

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149928T>A , CM000681.2:g.10149928T>A	GRCh38
NC_000019.9:g.10260604T>A , CM000681.1:g.10260604T>A	GRCh37
NC_000019.8:g.10121604T>A	NCBI36
NG_028016.3:g.86359A>T , LRG_362:g.86359A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2306A>T MANE Select	ENSP00000352516.3:p.Asp769Val
ENST00000586667.2:n.341A>T
ENST00000676604.1:n.1918A>T
ENST00000676610.1:c.2258A>T	ENSP00000504236.1:p.Asp753Val
ENST00000676820.1:n.2314A>T
ENST00000676868.1:n.2942A>T
ENST00000677013.1:c.*1948A>T	ENSP00000503135.1:n.*1948A>T
ENST00000677250.1:c.*1378A>T	ENSP00000502894.1:n.*1378A>T
ENST00000677616.1:c.1949A>T	ENSP00000503055.1:p.Asp650Val
ENST00000677634.1:c.2258A>T	ENSP00000504246.1:p.Asp753Val
ENST00000677685.1:c.*1483A>T	ENSP00000503407.1:n.*1483A>T
ENST00000677783.1:n.2728A>T
ENST00000677946.1:c.2258A>T	ENSP00000504202.1:p.Asp753Val
ENST00000678024.1:n.2401A>T
ENST00000678647.1:n.391A>T
ENST00000678694.1:n.1579A>T
ENST00000678804.1:c.2258A>T	ENSP00000503853.1:p.Asp753Val
ENST00000679100.1:n.445A>T
ENST00000679103.1:c.2258A>T	ENSP00000503151.1:p.Asp753Val
ENST00000679313.1:c.2258A>T	ENSP00000504512.1:p.Asp753Val
ENST00000340748.8:c.2258A>T	ENSP00000345739.3:p.Asp753Val
ENST00000359526.8:c.2306A>T	ENSP00000352516.3:p.Asp769Val
ENST00000540357.5:c.1250A>T	ENSP00000440457.2:p.Asp417Val
ENST00000586667.1:n.341A>T
ENST00000592705.5:c.*1996A>T	ENSP00000466657.1:n.*1996A>T
NM_001130823.1:c.2306A>T , LRG_362t1:c.2306A>T	NP_001124295.1:p.Asp769Val
NM_001379.2:c.2258A>T	NP_001370.1:p.Asp753Val
XM_011527772.1:c.2306A>T	XP_011526074.1:p.Asp769Val
XM_011527773.1:c.2258A>T	XP_011526075.1:p.Asp753Val
XM_011527774.1:c.1895A>T	XP_011526076.1:p.Asp632Val
NM_001130823.2:c.2306A>T	NP_001124295.1:p.Asp769Val
NM_001318730.1:c.2258A>T	NP_001305659.1:p.Asp753Val
NM_001318731.1:c.1943A>T	NP_001305660.1:p.Asp648Val
NM_001379.3:c.2258A>T	NP_001370.1:p.Asp753Val
NM_001130823.3:c.2306A>T MANE Select	NP_001124295.1:p.Asp769Val
NM_001318730.2:c.2258A>T	NP_001305659.1:p.Asp753Val
NM_001318731.2:c.1943A>T	NP_001305660.1:p.Asp648Val
NM_001379.4:c.2258A>T	NP_001370.1:p.Asp753Val