Canonical Allele Identifier: CA403976357

Gene: DNMT1

Linked Data

• COSMIC: COSM3821833 ; COSM5833590
• MyVariant Identifiers: chr19:g.10257157C>A (hg19) ; chr19:g.10146481C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146481C>A , CM000681.2:g.10146481C>A	GRCh38
NC_000019.9:g.10257157C>A , CM000681.1:g.10257157C>A	GRCh37
NC_000019.8:g.10118157C>A	NCBI36
NG_028016.3:g.89806G>T , LRG_362:g.89806G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2764G>T MANE Select	ENSP00000352516.3:p.Glu922Ter
ENST00000586667.2:n.799G>T
ENST00000676604.1:n.2376G>T
ENST00000676610.1:c.2716G>T	ENSP00000504236.1:p.Glu906Ter
ENST00000676820.1:n.2772G>T
ENST00000676868.1:n.3400G>T
ENST00000677013.1:c.*2406G>T	ENSP00000503135.1:n.*2406G>T
ENST00000677250.1:c.*1836G>T	ENSP00000502894.1:n.*1836G>T
ENST00000677616.1:c.2407G>T	ENSP00000503055.1:p.Glu803Ter
ENST00000677634.1:c.2716G>T	ENSP00000504246.1:p.Glu906Ter
ENST00000677685.1:c.*1941G>T	ENSP00000503407.1:n.*1941G>T
ENST00000677783.1:n.3186G>T
ENST00000677946.1:c.2716G>T	ENSP00000504202.1:p.Glu906Ter
ENST00000678024.1:n.2859G>T
ENST00000678647.1:n.849G>T
ENST00000678694.1:n.2037G>T
ENST00000678804.1:c.2716G>T	ENSP00000503853.1:p.Glu906Ter
ENST00000679100.1:n.903G>T
ENST00000679103.1:c.2716G>T	ENSP00000503151.1:p.Glu906Ter
ENST00000679313.1:c.2716G>T	ENSP00000504512.1:p.Glu906Ter
ENST00000340748.8:c.2716G>T	ENSP00000345739.3:p.Glu906Ter
ENST00000359526.8:c.2764G>T	ENSP00000352516.3:p.Glu922Ter
ENST00000540357.5:c.1708G>T	ENSP00000440457.2:p.Glu570Ter
ENST00000592705.5:c.*2454G>T	ENSP00000466657.1:n.*2454G>T
NM_001130823.1:c.2764G>T , LRG_362t1:c.2764G>T	NP_001124295.1:p.Glu922Ter
NM_001379.2:c.2716G>T	NP_001370.1:p.Glu906Ter
XM_011527772.1:c.2764G>T	XP_011526074.1:p.Glu922Ter
XM_011527773.1:c.2716G>T	XP_011526075.1:p.Glu906Ter
XM_011527774.1:c.2353G>T	XP_011526076.1:p.Glu785Ter
NM_001130823.2:c.2764G>T	NP_001124295.1:p.Glu922Ter
NM_001318730.1:c.2716G>T	NP_001305659.1:p.Glu906Ter
NM_001318731.1:c.2401G>T	NP_001305660.1:p.Glu801Ter
NM_001379.3:c.2716G>T	NP_001370.1:p.Glu906Ter
NM_001130823.3:c.2764G>T MANE Select	NP_001124295.1:p.Glu922Ter
NM_001318730.2:c.2716G>T	NP_001305659.1:p.Glu906Ter
NM_001318731.2:c.2401G>T	NP_001305660.1:p.Glu801Ter
NM_001379.4:c.2716G>T	NP_001370.1:p.Glu906Ter