Canonical Allele Identifier: CA2322290208

Gene: DNMT1

Linked Data

• dbSNP Id: rs1417873308

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156163_10156166del , CM000681.2:g.10156163_10156166del	GRCh38
NC_000019.9:g.10266839_10266842del , CM000681.1:g.10266839_10266842del	GRCh37
NC_000019.8:g.10127839_10127842del	NCBI36
NG_028016.3:g.80123_80126del , LRG_362:g.80123_80126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-219_1400-216del MANE Select	ENSP00000352516.3:n.1400-219_1400-216del
ENST00000676604.1:n.1012-219_1012-216del
ENST00000676610.1:c.1352-219_1352-216del	ENSP00000504236.1:n.1352-219_1352-216del
ENST00000676820.1:n.1408-219_1408-216del
ENST00000676868.1:n.2036-219_2036-216del
ENST00000677013.1:c.*1042-219_*1042-216del	ENSP00000503135.1:n.*1042-219_*1042-216del
ENST00000677250.1:c.*472-219_*472-216del	ENSP00000502894.1:n.*472-219_*472-216del
ENST00000677616.1:c.1043-219_1043-216del	ENSP00000503055.1:n.1043-219_1043-216del
ENST00000677634.1:c.1352-219_1352-216del	ENSP00000504246.1:n.1352-219_1352-216del
ENST00000677685.1:c.*577-219_*577-216del	ENSP00000503407.1:n.*577-219_*577-216del
ENST00000677783.1:n.1822-219_1822-216del
ENST00000677946.1:c.1352-219_1352-216del	ENSP00000504202.1:n.1352-219_1352-216del
ENST00000678024.1:n.1495-219_1495-216del
ENST00000678694.1:n.673-219_673-216del
ENST00000678804.1:c.1352-219_1352-216del	ENSP00000503853.1:n.1352-219_1352-216del
ENST00000679103.1:c.1352-219_1352-216del	ENSP00000503151.1:n.1352-219_1352-216del
ENST00000679313.1:c.1352-219_1352-216del	ENSP00000504512.1:n.1352-219_1352-216del
ENST00000340748.8:c.1352-219_1352-216del	ENSP00000345739.3:n.1352-219_1352-216del
ENST00000359526.8:c.1400-219_1400-216del	ENSP00000352516.3:n.1400-219_1400-216del
ENST00000540357.5:c.344-219_344-216del	ENSP00000440457.2:n.344-219_344-216del
ENST00000585843.1:n.557-219_557-216del
ENST00000592705.5:c.*1090-219_*1090-216del	ENSP00000466657.1:n.*1090-219_*1090-216del
NM_001130823.1:c.1400-219_1400-216del , LRG_362t1:c.1400-219_1400-216del	NP_001124295.1:n.1400-219_1400-216del
NM_001379.2:c.1352-219_1352-216del	NP_001370.1:n.1352-219_1352-216del
XM_011527772.1:c.1400-219_1400-216del	XP_011526074.1:n.1400-219_1400-216del
XM_011527773.1:c.1352-219_1352-216del	XP_011526075.1:n.1352-219_1352-216del
XM_011527774.1:c.989-219_989-216del	XP_011526076.1:n.989-219_989-216del
NM_001130823.2:c.1400-219_1400-216del	NP_001124295.1:n.1400-219_1400-216del
NM_001318730.1:c.1352-219_1352-216del	NP_001305659.1:n.1352-219_1352-216del
NM_001318731.1:c.1037-219_1037-216del	NP_001305660.1:n.1037-219_1037-216del
NM_001379.3:c.1352-219_1352-216del	NP_001370.1:n.1352-219_1352-216del
NM_001130823.3:c.1400-219_1400-216del MANE Select	NP_001124295.1:n.1400-219_1400-216del
NM_001318730.2:c.1352-219_1352-216del	NP_001305659.1:n.1352-219_1352-216del
NM_001318731.2:c.1037-219_1037-216del	NP_001305660.1:n.1037-219_1037-216del
NM_001379.4:c.1352-219_1352-216del	NP_001370.1:n.1352-219_1352-216del