Canonical Allele Identifier: CA403938126

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267112A>T (hg19) ; chr19:g.10156436A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156436A>T , CM000681.2:g.10156436A>T	GRCh38
NC_000019.9:g.10267112A>T , CM000681.1:g.10267112A>T	GRCh37
NC_000019.8:g.10128112A>T	NCBI36
NG_028016.3:g.79851T>A , LRG_362:g.79851T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1354T>A MANE Select	ENSP00000352516.3:p.Ser452Thr
ENST00000676604.1:n.966T>A
ENST00000676610.1:c.1306T>A	ENSP00000504236.1:p.Ser436Thr
ENST00000676820.1:n.1362T>A
ENST00000676868.1:n.1990T>A
ENST00000677013.1:c.*996T>A	ENSP00000503135.1:n.*996T>A
ENST00000677250.1:c.*426T>A	ENSP00000502894.1:n.*426T>A
ENST00000677616.1:c.997T>A	ENSP00000503055.1:p.Ser333Thr
ENST00000677634.1:c.1306T>A	ENSP00000504246.1:p.Ser436Thr
ENST00000677685.1:c.*531T>A	ENSP00000503407.1:n.*531T>A
ENST00000677783.1:n.1776T>A
ENST00000677946.1:c.1306T>A	ENSP00000504202.1:p.Ser436Thr
ENST00000678024.1:n.1449T>A
ENST00000678694.1:n.627T>A
ENST00000678804.1:c.1306T>A	ENSP00000503853.1:p.Ser436Thr
ENST00000679103.1:c.1306T>A	ENSP00000503151.1:p.Ser436Thr
ENST00000679313.1:c.1306T>A	ENSP00000504512.1:p.Ser436Thr
ENST00000340748.8:c.1306T>A	ENSP00000345739.3:p.Ser436Thr
ENST00000359526.8:c.1354T>A	ENSP00000352516.3:p.Ser452Thr
ENST00000540357.5:c.298T>A	ENSP00000440457.2:p.Ser100Thr
ENST00000585843.1:n.511T>A
ENST00000592705.5:c.*1044T>A	ENSP00000466657.1:n.*1044T>A
NM_001130823.1:c.1354T>A , LRG_362t1:c.1354T>A	NP_001124295.1:p.Ser452Thr
NM_001379.2:c.1306T>A	NP_001370.1:p.Ser436Thr
XM_011527772.1:c.1354T>A	XP_011526074.1:p.Ser452Thr
XM_011527773.1:c.1306T>A	XP_011526075.1:p.Ser436Thr
XM_011527774.1:c.943T>A	XP_011526076.1:p.Ser315Thr
NM_001130823.2:c.1354T>A	NP_001124295.1:p.Ser452Thr
NM_001318730.1:c.1306T>A	NP_001305659.1:p.Ser436Thr
NM_001318731.1:c.991T>A	NP_001305660.1:p.Ser331Thr
NM_001379.3:c.1306T>A	NP_001370.1:p.Ser436Thr
NM_001130823.3:c.1354T>A MANE Select	NP_001124295.1:p.Ser452Thr
NM_001318730.2:c.1306T>A	NP_001305659.1:p.Ser436Thr
NM_001318731.2:c.991T>A	NP_001305660.1:p.Ser331Thr
NM_001379.4:c.1306T>A	NP_001370.1:p.Ser436Thr