Canonical Allele Identifier: CA2588330367

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10156072-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156072_10156073insG , CM000681.2:g.10156072_10156073insG	GRCh38
NC_000019.9:g.10266748_10266749insG , CM000681.1:g.10266748_10266749insG	GRCh37
NC_000019.8:g.10127748_10127749insG	NCBI36
NG_028016.3:g.80214_80215insC , LRG_362:g.80214_80215insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-128_1400-127insC MANE Select	ENSP00000352516.3:n.1400-128_1400-127insC
ENST00000676604.1:n.1012-128_1012-127insC
ENST00000676610.1:c.1352-128_1352-127insC	ENSP00000504236.1:n.1352-128_1352-127insC
ENST00000676820.1:n.1408-128_1408-127insC
ENST00000676868.1:n.2036-128_2036-127insC
ENST00000677013.1:c.*1042-128_*1042-127insC	ENSP00000503135.1:n.*1042-128_*1042-127insC
ENST00000677250.1:c.*472-128_*472-127insC	ENSP00000502894.1:n.*472-128_*472-127insC
ENST00000677616.1:c.1043-128_1043-127insC	ENSP00000503055.1:n.1043-128_1043-127insC
ENST00000677634.1:c.1352-128_1352-127insC	ENSP00000504246.1:n.1352-128_1352-127insC
ENST00000677685.1:c.*577-128_*577-127insC	ENSP00000503407.1:n.*577-128_*577-127insC
ENST00000677783.1:n.1822-128_1822-127insC
ENST00000677946.1:c.1352-128_1352-127insC	ENSP00000504202.1:n.1352-128_1352-127insC
ENST00000678024.1:n.1495-128_1495-127insC
ENST00000678694.1:n.673-128_673-127insC
ENST00000678804.1:c.1352-128_1352-127insC	ENSP00000503853.1:n.1352-128_1352-127insC
ENST00000679103.1:c.1352-128_1352-127insC	ENSP00000503151.1:n.1352-128_1352-127insC
ENST00000679313.1:c.1352-128_1352-127insC	ENSP00000504512.1:n.1352-128_1352-127insC
ENST00000340748.8:c.1352-128_1352-127insC	ENSP00000345739.3:n.1352-128_1352-127insC
ENST00000359526.8:c.1400-128_1400-127insC	ENSP00000352516.3:n.1400-128_1400-127insC
ENST00000540357.5:c.344-128_344-127insC	ENSP00000440457.2:n.344-128_344-127insC
ENST00000585843.1:n.557-128_557-127insC
ENST00000592705.5:c.*1090-128_*1090-127insC	ENSP00000466657.1:n.*1090-128_*1090-127insC
NM_001130823.1:c.1400-128_1400-127insC , LRG_362t1:c.1400-128_1400-127insC	NP_001124295.1:n.1400-128_1400-127insC
NM_001379.2:c.1352-128_1352-127insC	NP_001370.1:n.1352-128_1352-127insC
XM_011527772.1:c.1400-128_1400-127insC	XP_011526074.1:n.1400-128_1400-127insC
XM_011527773.1:c.1352-128_1352-127insC	XP_011526075.1:n.1352-128_1352-127insC
XM_011527774.1:c.989-128_989-127insC	XP_011526076.1:n.989-128_989-127insC
NM_001130823.2:c.1400-128_1400-127insC	NP_001124295.1:n.1400-128_1400-127insC
NM_001318730.1:c.1352-128_1352-127insC	NP_001305659.1:n.1352-128_1352-127insC
NM_001318731.1:c.1037-128_1037-127insC	NP_001305660.1:n.1037-128_1037-127insC
NM_001379.3:c.1352-128_1352-127insC	NP_001370.1:n.1352-128_1352-127insC
NM_001130823.3:c.1400-128_1400-127insC MANE Select	NP_001124295.1:n.1400-128_1400-127insC
NM_001318730.2:c.1352-128_1352-127insC	NP_001305659.1:n.1352-128_1352-127insC
NM_001318731.2:c.1037-128_1037-127insC	NP_001305660.1:n.1037-128_1037-127insC
NM_001379.4:c.1352-128_1352-127insC	NP_001370.1:n.1352-128_1352-127insC