Canonical Allele Identifier: CA403976339

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257150G>C (hg19) ; chr19:g.10146474G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146474G>C , CM000681.2:g.10146474G>C	GRCh38
NC_000019.9:g.10257150G>C , CM000681.1:g.10257150G>C	GRCh37
NC_000019.8:g.10118150G>C	NCBI36
NG_028016.3:g.89813C>G , LRG_362:g.89813C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2771C>G MANE Select	ENSP00000352516.3:p.Pro924Arg
ENST00000586667.2:n.806C>G
ENST00000676604.1:n.2383C>G
ENST00000676610.1:c.2723C>G	ENSP00000504236.1:p.Pro908Arg
ENST00000676820.1:n.2779C>G
ENST00000676868.1:n.3407C>G
ENST00000677013.1:c.*2413C>G	ENSP00000503135.1:n.*2413C>G
ENST00000677250.1:c.*1843C>G	ENSP00000502894.1:n.*1843C>G
ENST00000677616.1:c.2414C>G	ENSP00000503055.1:p.Pro805Arg
ENST00000677634.1:c.2723C>G	ENSP00000504246.1:p.Pro908Arg
ENST00000677685.1:c.*1948C>G	ENSP00000503407.1:n.*1948C>G
ENST00000677783.1:n.3193C>G
ENST00000677946.1:c.2723C>G	ENSP00000504202.1:p.Pro908Arg
ENST00000678024.1:n.2866C>G
ENST00000678647.1:n.856C>G
ENST00000678694.1:n.2044C>G
ENST00000678804.1:c.2723C>G	ENSP00000503853.1:p.Pro908Arg
ENST00000679100.1:n.910C>G
ENST00000679103.1:c.2723C>G	ENSP00000503151.1:p.Pro908Arg
ENST00000679313.1:c.2723C>G	ENSP00000504512.1:p.Pro908Arg
ENST00000340748.8:c.2723C>G	ENSP00000345739.3:p.Pro908Arg
ENST00000359526.8:c.2771C>G	ENSP00000352516.3:p.Pro924Arg
ENST00000540357.5:c.1715C>G	ENSP00000440457.2:p.Pro572Arg
ENST00000592705.5:c.*2461C>G	ENSP00000466657.1:n.*2461C>G
NM_001130823.1:c.2771C>G , LRG_362t1:c.2771C>G	NP_001124295.1:p.Pro924Arg
NM_001379.2:c.2723C>G	NP_001370.1:p.Pro908Arg
XM_011527772.1:c.2771C>G	XP_011526074.1:p.Pro924Arg
XM_011527773.1:c.2723C>G	XP_011526075.1:p.Pro908Arg
XM_011527774.1:c.2360C>G	XP_011526076.1:p.Pro787Arg
NM_001130823.2:c.2771C>G	NP_001124295.1:p.Pro924Arg
NM_001318730.1:c.2723C>G	NP_001305659.1:p.Pro908Arg
NM_001318731.1:c.2408C>G	NP_001305660.1:p.Pro803Arg
NM_001379.3:c.2723C>G	NP_001370.1:p.Pro908Arg
NM_001130823.3:c.2771C>G MANE Select	NP_001124295.1:p.Pro924Arg
NM_001318730.2:c.2723C>G	NP_001305659.1:p.Pro908Arg
NM_001318731.2:c.2408C>G	NP_001305660.1:p.Pro803Arg
NM_001379.4:c.2723C>G	NP_001370.1:p.Pro908Arg