Canonical Allele Identifier: CA403976343

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257151G>T (hg19) ; chr19:g.10146475G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146475G>T , CM000681.2:g.10146475G>T	GRCh38
NC_000019.9:g.10257151G>T , CM000681.1:g.10257151G>T	GRCh37
NC_000019.8:g.10118151G>T	NCBI36
NG_028016.3:g.89812C>A , LRG_362:g.89812C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2770C>A MANE Select	ENSP00000352516.3:p.Pro924Thr
ENST00000586667.2:n.805C>A
ENST00000676604.1:n.2382C>A
ENST00000676610.1:c.2722C>A	ENSP00000504236.1:p.Pro908Thr
ENST00000676820.1:n.2778C>A
ENST00000676868.1:n.3406C>A
ENST00000677013.1:c.*2412C>A	ENSP00000503135.1:n.*2412C>A
ENST00000677250.1:c.*1842C>A	ENSP00000502894.1:n.*1842C>A
ENST00000677616.1:c.2413C>A	ENSP00000503055.1:p.Pro805Thr
ENST00000677634.1:c.2722C>A	ENSP00000504246.1:p.Pro908Thr
ENST00000677685.1:c.*1947C>A	ENSP00000503407.1:n.*1947C>A
ENST00000677783.1:n.3192C>A
ENST00000677946.1:c.2722C>A	ENSP00000504202.1:p.Pro908Thr
ENST00000678024.1:n.2865C>A
ENST00000678647.1:n.855C>A
ENST00000678694.1:n.2043C>A
ENST00000678804.1:c.2722C>A	ENSP00000503853.1:p.Pro908Thr
ENST00000679100.1:n.909C>A
ENST00000679103.1:c.2722C>A	ENSP00000503151.1:p.Pro908Thr
ENST00000679313.1:c.2722C>A	ENSP00000504512.1:p.Pro908Thr
ENST00000340748.8:c.2722C>A	ENSP00000345739.3:p.Pro908Thr
ENST00000359526.8:c.2770C>A	ENSP00000352516.3:p.Pro924Thr
ENST00000540357.5:c.1714C>A	ENSP00000440457.2:p.Pro572Thr
ENST00000592705.5:c.*2460C>A	ENSP00000466657.1:n.*2460C>A
NM_001130823.1:c.2770C>A , LRG_362t1:c.2770C>A	NP_001124295.1:p.Pro924Thr
NM_001379.2:c.2722C>A	NP_001370.1:p.Pro908Thr
XM_011527772.1:c.2770C>A	XP_011526074.1:p.Pro924Thr
XM_011527773.1:c.2722C>A	XP_011526075.1:p.Pro908Thr
XM_011527774.1:c.2359C>A	XP_011526076.1:p.Pro787Thr
NM_001130823.2:c.2770C>A	NP_001124295.1:p.Pro924Thr
NM_001318730.1:c.2722C>A	NP_001305659.1:p.Pro908Thr
NM_001318731.1:c.2407C>A	NP_001305660.1:p.Pro803Thr
NM_001379.3:c.2722C>A	NP_001370.1:p.Pro908Thr
NM_001130823.3:c.2770C>A MANE Select	NP_001124295.1:p.Pro924Thr
NM_001318730.2:c.2722C>A	NP_001305659.1:p.Pro908Thr
NM_001318731.2:c.2407C>A	NP_001305660.1:p.Pro803Thr
NM_001379.4:c.2722C>A	NP_001370.1:p.Pro908Thr