Canonical Allele Identifier: CA9188194

Gene: DNMT1

Linked Data

• dbSNP Id: rs761229261
• ExAC: 19:10265196 G / A
• gnomAD v2: 19-10265196-G-A
• gnomAD v3: 19-10154520-G-A
• gnomAD v4: 19-10154520-G-A
• MyVariant Identifiers: chr19:g.10265196G>A (hg19) ; chr19:g.10154520G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154520G>A , CM000681.2:g.10154520G>A	GRCh38
NC_000019.9:g.10265196G>A , CM000681.1:g.10265196G>A	GRCh37
NC_000019.8:g.10126196G>A	NCBI36
NG_028016.3:g.81767C>T , LRG_362:g.81767C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.1833-41C>T MANE Select	ENSP00000352516.3:n.1833-41C>T
ENST00000676604.1:n.1445-41C>T
ENST00000676610.1:c.1785-41C>T	ENSP00000504236.1:n.1785-41C>T
ENST00000676820.1:n.1841-41C>T
ENST00000676868.1:n.2469-41C>T
ENST00000677013.1:c.*1475-41C>T	ENSP00000503135.1:n.*1475-41C>T
ENST00000677250.1:c.*905-41C>T	ENSP00000502894.1:n.*905-41C>T
ENST00000677616.1:c.1476-41C>T	ENSP00000503055.1:n.1476-41C>T
ENST00000677634.1:c.1785-41C>T	ENSP00000504246.1:n.1785-41C>T
ENST00000677685.1:c.*1010-41C>T	ENSP00000503407.1:n.*1010-41C>T
ENST00000677783.1:n.2255-41C>T
ENST00000677946.1:c.1785-41C>T	ENSP00000504202.1:n.1785-41C>T
ENST00000678024.1:n.1928-41C>T
ENST00000678694.1:n.1106-41C>T
ENST00000678804.1:c.1785-41C>T	ENSP00000503853.1:n.1785-41C>T
ENST00000679103.1:c.1785-41C>T	ENSP00000503151.1:n.1785-41C>T
ENST00000679313.1:c.1785-41C>T	ENSP00000504512.1:n.1785-41C>T
ENST00000340748.8:c.1785-41C>T	ENSP00000345739.3:n.1785-41C>T
ENST00000359526.8:c.1833-41C>T	ENSP00000352516.3:n.1833-41C>T
ENST00000540357.5:c.777-41C>T	ENSP00000440457.2:n.777-41C>T
ENST00000586799.1:c.219-41C>T
ENST00000592705.5:c.*1523-41C>T	ENSP00000466657.1:n.*1523-41C>T
NM_001130823.1:c.1833-41C>T , LRG_362t1:c.1833-41C>T	NP_001124295.1:n.1833-41C>T
NM_001379.2:c.1785-41C>T	NP_001370.1:n.1785-41C>T
XM_011527772.1:c.1833-41C>T	XP_011526074.1:n.1833-41C>T
XM_011527773.1:c.1785-41C>T	XP_011526075.1:n.1785-41C>T
XM_011527774.1:c.1422-41C>T	XP_011526076.1:n.1422-41C>T
NM_001130823.2:c.1833-41C>T	NP_001124295.1:n.1833-41C>T
NM_001318730.1:c.1785-41C>T	NP_001305659.1:n.1785-41C>T
NM_001318731.1:c.1470-41C>T	NP_001305660.1:n.1470-41C>T
NM_001379.3:c.1785-41C>T	NP_001370.1:n.1785-41C>T
NM_001130823.3:c.1833-41C>T MANE Select	NP_001124295.1:n.1833-41C>T
NM_001318730.2:c.1785-41C>T	NP_001305659.1:n.1785-41C>T
NM_001318731.2:c.1470-41C>T	NP_001305660.1:n.1470-41C>T
NM_001379.4:c.1785-41C>T	NP_001370.1:n.1785-41C>T