Canonical Allele Identifier: CA505467399

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10265264C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154588C>T , CM000681.2:g.10154588C>T	GRCh38
NC_000019.9:g.10265264C>T , CM000681.1:g.10265264C>T	GRCh37
NC_000019.8:g.10126264C>T	NCBI36
NG_028016.3:g.81699G>A , LRG_362:g.81699G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1830G>A MANE Select	ENSP00000352516.3:p.Gln610=
ENST00000676604.1:n.1442G>A
ENST00000676610.1:c.1782G>A	ENSP00000504236.1:p.Gln594=
ENST00000676820.1:n.1838G>A
ENST00000676868.1:n.2466G>A
ENST00000677013.1:c.*1472G>A	ENSP00000503135.1:n.*1472G>A
ENST00000677250.1:c.*902G>A	ENSP00000502894.1:n.*902G>A
ENST00000677616.1:c.1473G>A	ENSP00000503055.1:p.Gln491=
ENST00000677634.1:c.1782G>A	ENSP00000504246.1:p.Gln594=
ENST00000677685.1:c.*1007G>A	ENSP00000503407.1:n.*1007G>A
ENST00000677783.1:n.2252G>A
ENST00000677946.1:c.1782G>A	ENSP00000504202.1:p.Gln594=
ENST00000678024.1:n.1925G>A
ENST00000678694.1:n.1103G>A
ENST00000678804.1:c.1782G>A	ENSP00000503853.1:p.Gln594=
ENST00000679103.1:c.1782G>A	ENSP00000503151.1:p.Gln594=
ENST00000679313.1:c.1782G>A	ENSP00000504512.1:p.Gln594=
ENST00000340748.8:c.1782G>A	ENSP00000345739.3:p.Gln594=
ENST00000359526.8:c.1830G>A	ENSP00000352516.3:p.Gln610=
ENST00000540357.5:c.774G>A	ENSP00000440457.2:p.Gln258=
ENST00000586799.1:c.216G>A
ENST00000592705.5:c.*1520G>A	ENSP00000466657.1:n.*1520G>A
NM_001130823.1:c.1830G>A , LRG_362t1:c.1830G>A	NP_001124295.1:p.Gln610=
NM_001379.2:c.1782G>A	NP_001370.1:p.Gln594=
XM_011527772.1:c.1830G>A	XP_011526074.1:p.Gln610=
XM_011527773.1:c.1782G>A	XP_011526075.1:p.Gln594=
XM_011527774.1:c.1419G>A	XP_011526076.1:p.Gln473=
NM_001130823.2:c.1830G>A	NP_001124295.1:p.Gln610=
NM_001318730.1:c.1782G>A	NP_001305659.1:p.Gln594=
NM_001318731.1:c.1467G>A	NP_001305660.1:p.Gln489=
NM_001379.3:c.1782G>A	NP_001370.1:p.Gln594=
NM_001130823.3:c.1830G>A MANE Select	NP_001124295.1:p.Gln610=
NM_001318730.2:c.1782G>A	NP_001305659.1:p.Gln594=
NM_001318731.2:c.1467G>A	NP_001305660.1:p.Gln489=
NM_001379.4:c.1782G>A	NP_001370.1:p.Gln594=