Canonical Allele Identifier: CA2588330377

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10156078-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156078_10156079insG , CM000681.2:g.10156078_10156079insG	GRCh38
NC_000019.9:g.10266754_10266755insG , CM000681.1:g.10266754_10266755insG	GRCh37
NC_000019.8:g.10127754_10127755insG	NCBI36
NG_028016.3:g.80208_80209insC , LRG_362:g.80208_80209insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-134_1400-133insC MANE Select	ENSP00000352516.3:n.1400-134_1400-133insC
ENST00000676604.1:n.1012-134_1012-133insC
ENST00000676610.1:c.1352-134_1352-133insC	ENSP00000504236.1:n.1352-134_1352-133insC
ENST00000676820.1:n.1408-134_1408-133insC
ENST00000676868.1:n.2036-134_2036-133insC
ENST00000677013.1:c.*1042-134_*1042-133insC	ENSP00000503135.1:n.*1042-134_*1042-133insC
ENST00000677250.1:c.*472-134_*472-133insC	ENSP00000502894.1:n.*472-134_*472-133insC
ENST00000677616.1:c.1043-134_1043-133insC	ENSP00000503055.1:n.1043-134_1043-133insC
ENST00000677634.1:c.1352-134_1352-133insC	ENSP00000504246.1:n.1352-134_1352-133insC
ENST00000677685.1:c.*577-134_*577-133insC	ENSP00000503407.1:n.*577-134_*577-133insC
ENST00000677783.1:n.1822-134_1822-133insC
ENST00000677946.1:c.1352-134_1352-133insC	ENSP00000504202.1:n.1352-134_1352-133insC
ENST00000678024.1:n.1495-134_1495-133insC
ENST00000678694.1:n.673-134_673-133insC
ENST00000678804.1:c.1352-134_1352-133insC	ENSP00000503853.1:n.1352-134_1352-133insC
ENST00000679103.1:c.1352-134_1352-133insC	ENSP00000503151.1:n.1352-134_1352-133insC
ENST00000679313.1:c.1352-134_1352-133insC	ENSP00000504512.1:n.1352-134_1352-133insC
ENST00000340748.8:c.1352-134_1352-133insC	ENSP00000345739.3:n.1352-134_1352-133insC
ENST00000359526.8:c.1400-134_1400-133insC	ENSP00000352516.3:n.1400-134_1400-133insC
ENST00000540357.5:c.344-134_344-133insC	ENSP00000440457.2:n.344-134_344-133insC
ENST00000585843.1:n.557-134_557-133insC
ENST00000592705.5:c.*1090-134_*1090-133insC	ENSP00000466657.1:n.*1090-134_*1090-133insC
NM_001130823.1:c.1400-134_1400-133insC , LRG_362t1:c.1400-134_1400-133insC	NP_001124295.1:n.1400-134_1400-133insC
NM_001379.2:c.1352-134_1352-133insC	NP_001370.1:n.1352-134_1352-133insC
XM_011527772.1:c.1400-134_1400-133insC	XP_011526074.1:n.1400-134_1400-133insC
XM_011527773.1:c.1352-134_1352-133insC	XP_011526075.1:n.1352-134_1352-133insC
XM_011527774.1:c.989-134_989-133insC	XP_011526076.1:n.989-134_989-133insC
NM_001130823.2:c.1400-134_1400-133insC	NP_001124295.1:n.1400-134_1400-133insC
NM_001318730.1:c.1352-134_1352-133insC	NP_001305659.1:n.1352-134_1352-133insC
NM_001318731.1:c.1037-134_1037-133insC	NP_001305660.1:n.1037-134_1037-133insC
NM_001379.3:c.1352-134_1352-133insC	NP_001370.1:n.1352-134_1352-133insC
NM_001130823.3:c.1400-134_1400-133insC MANE Select	NP_001124295.1:n.1400-134_1400-133insC
NM_001318730.2:c.1352-134_1352-133insC	NP_001305659.1:n.1352-134_1352-133insC
NM_001318731.2:c.1037-134_1037-133insC	NP_001305660.1:n.1037-134_1037-133insC
NM_001379.4:c.1352-134_1352-133insC	NP_001370.1:n.1352-134_1352-133insC