Canonical Allele Identifier: CA9187827

Gene: DNMT1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10142180C>T , CM000681.2:g.10142180C>T	GRCh38
NC_000019.9:g.10252856C>T , CM000681.1:g.10252856C>T	GRCh37
NC_000019.8:g.10113856C>T	NCBI36
NG_028016.3:g.94107G>A , LRG_362:g.94107G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.3157G>A MANE Select	ENSP00000352516.3:p.Ala1053Thr
ENST00000586667.2:n.1192G>A
ENST00000676604.1:n.2769G>A
ENST00000676610.1:c.3109G>A	ENSP00000504236.1:p.Ala1037Thr
ENST00000676820.1:n.3165G>A
ENST00000676868.1:n.3793G>A
ENST00000677013.1:c.*2799G>A	ENSP00000503135.1:n.*2799G>A
ENST00000677250.1:c.*2229G>A	ENSP00000502894.1:n.*2229G>A
ENST00000677616.1:c.2800G>A	ENSP00000503055.1:p.Ala934Thr
ENST00000677634.1:c.3109G>A	ENSP00000504246.1:p.Ala1037Thr
ENST00000677685.1:c.*2334G>A	ENSP00000503407.1:n.*2334G>A
ENST00000677783.1:n.3579G>A
ENST00000677946.1:c.3109G>A	ENSP00000504202.1:p.Ala1037Thr
ENST00000678024.1:n.3252G>A
ENST00000678647.1:n.1242G>A
ENST00000678694.1:n.2430G>A
ENST00000678804.1:c.3109G>A	ENSP00000503853.1:p.Ala1037Thr
ENST00000679100.1:n.1296G>A
ENST00000679103.1:c.3109G>A	ENSP00000503151.1:p.Ala1037Thr
ENST00000679313.1:c.3109G>A	ENSP00000504512.1:p.Ala1037Thr
ENST00000340748.8:c.3109G>A	ENSP00000345739.3:p.Ala1037Thr
ENST00000359526.8:c.3157G>A	ENSP00000352516.3:p.Ala1053Thr
ENST00000540357.5:c.2101G>A	ENSP00000440457.2:p.Ala701Thr
ENST00000586588.5:n.1030G>A
ENST00000589538.5:n.177G>A
ENST00000591239.1:n.67G>A
ENST00000592705.5:c.*2847G>A	ENSP00000466657.1:n.*2847G>A
ENST00000593049.5:n.119G>A
NM_001130823.1:c.3157G>A , LRG_362t1:c.3157G>A	NP_001124295.1:p.Ala1053Thr
NM_001379.2:c.3109G>A	NP_001370.1:p.Ala1037Thr
XM_011527772.1:c.3157G>A	XP_011526074.1:p.Ala1053Thr
XM_011527773.1:c.3109G>A	XP_011526075.1:p.Ala1037Thr
XM_011527774.1:c.2746G>A	XP_011526076.1:p.Ala916Thr
NM_001130823.2:c.3157G>A	NP_001124295.1:p.Ala1053Thr
NM_001318730.1:c.3109G>A	NP_001305659.1:p.Ala1037Thr
NM_001318731.1:c.2794G>A	NP_001305660.1:p.Ala932Thr
NM_001379.3:c.3109G>A	NP_001370.1:p.Ala1037Thr
NM_001130823.3:c.3157G>A MANE Select	NP_001124295.1:p.Ala1053Thr
NM_001318730.2:c.3109G>A	NP_001305659.1:p.Ala1037Thr
NM_001318731.2:c.2794G>A	NP_001305660.1:p.Ala932Thr
NM_001379.4:c.3109G>A	NP_001370.1:p.Ala1037Thr