Canonical Allele Identifier: CA505382447

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257148T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146472T>G , CM000681.2:g.10146472T>G	GRCh38
NC_000019.9:g.10257148T>G , CM000681.1:g.10257148T>G	GRCh37
NC_000019.8:g.10118148T>G	NCBI36
NG_028016.3:g.89815A>C , LRG_362:g.89815A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2773A>C MANE Select	ENSP00000352516.3:p.Arg925=
ENST00000586667.2:n.808A>C
ENST00000676604.1:n.2385A>C
ENST00000676610.1:c.2725A>C	ENSP00000504236.1:p.Arg909=
ENST00000676820.1:n.2781A>C
ENST00000676868.1:n.3409A>C
ENST00000677013.1:c.*2415A>C	ENSP00000503135.1:n.*2415A>C
ENST00000677250.1:c.*1845A>C	ENSP00000502894.1:n.*1845A>C
ENST00000677616.1:c.2416A>C	ENSP00000503055.1:p.Arg806=
ENST00000677634.1:c.2725A>C	ENSP00000504246.1:p.Arg909=
ENST00000677685.1:c.*1950A>C	ENSP00000503407.1:n.*1950A>C
ENST00000677783.1:n.3195A>C
ENST00000677946.1:c.2725A>C	ENSP00000504202.1:p.Arg909=
ENST00000678024.1:n.2868A>C
ENST00000678647.1:n.858A>C
ENST00000678694.1:n.2046A>C
ENST00000678804.1:c.2725A>C	ENSP00000503853.1:p.Arg909=
ENST00000679100.1:n.912A>C
ENST00000679103.1:c.2725A>C	ENSP00000503151.1:p.Arg909=
ENST00000679313.1:c.2725A>C	ENSP00000504512.1:p.Arg909=
ENST00000340748.8:c.2725A>C	ENSP00000345739.3:p.Arg909=
ENST00000359526.8:c.2773A>C	ENSP00000352516.3:p.Arg925=
ENST00000540357.5:c.1717A>C	ENSP00000440457.2:p.Arg573=
ENST00000592705.5:c.*2463A>C	ENSP00000466657.1:n.*2463A>C
NM_001130823.1:c.2773A>C , LRG_362t1:c.2773A>C	NP_001124295.1:p.Arg925=
NM_001379.2:c.2725A>C	NP_001370.1:p.Arg909=
XM_011527772.1:c.2773A>C	XP_011526074.1:p.Arg925=
XM_011527773.1:c.2725A>C	XP_011526075.1:p.Arg909=
XM_011527774.1:c.2362A>C	XP_011526076.1:p.Arg788=
NM_001130823.2:c.2773A>C	NP_001124295.1:p.Arg925=
NM_001318730.1:c.2725A>C	NP_001305659.1:p.Arg909=
NM_001318731.1:c.2410A>C	NP_001305660.1:p.Arg804=
NM_001379.3:c.2725A>C	NP_001370.1:p.Arg909=
NM_001130823.3:c.2773A>C MANE Select	NP_001124295.1:p.Arg925=
NM_001318730.2:c.2725A>C	NP_001305659.1:p.Arg909=
NM_001318731.2:c.2410A>C	NP_001305660.1:p.Arg804=
NM_001379.4:c.2725A>C	NP_001370.1:p.Arg909=