Canonical Allele Identifier: CA2588330380

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10156080-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156080_10156081insT , CM000681.2:g.10156080_10156081insT	GRCh38
NC_000019.9:g.10266756_10266757insT , CM000681.1:g.10266756_10266757insT	GRCh37
NC_000019.8:g.10127756_10127757insT	NCBI36
NG_028016.3:g.80206_80207insA , LRG_362:g.80206_80207insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-136_1400-135insA MANE Select	ENSP00000352516.3:n.1400-136_1400-135insA
ENST00000676604.1:n.1012-136_1012-135insA
ENST00000676610.1:c.1352-136_1352-135insA	ENSP00000504236.1:n.1352-136_1352-135insA
ENST00000676820.1:n.1408-136_1408-135insA
ENST00000676868.1:n.2036-136_2036-135insA
ENST00000677013.1:c.*1042-136_*1042-135insA	ENSP00000503135.1:n.*1042-136_*1042-135insA
ENST00000677250.1:c.*472-136_*472-135insA	ENSP00000502894.1:n.*472-136_*472-135insA
ENST00000677616.1:c.1043-136_1043-135insA	ENSP00000503055.1:n.1043-136_1043-135insA
ENST00000677634.1:c.1352-136_1352-135insA	ENSP00000504246.1:n.1352-136_1352-135insA
ENST00000677685.1:c.*577-136_*577-135insA	ENSP00000503407.1:n.*577-136_*577-135insA
ENST00000677783.1:n.1822-136_1822-135insA
ENST00000677946.1:c.1352-136_1352-135insA	ENSP00000504202.1:n.1352-136_1352-135insA
ENST00000678024.1:n.1495-136_1495-135insA
ENST00000678694.1:n.673-136_673-135insA
ENST00000678804.1:c.1352-136_1352-135insA	ENSP00000503853.1:n.1352-136_1352-135insA
ENST00000679103.1:c.1352-136_1352-135insA	ENSP00000503151.1:n.1352-136_1352-135insA
ENST00000679313.1:c.1352-136_1352-135insA	ENSP00000504512.1:n.1352-136_1352-135insA
ENST00000340748.8:c.1352-136_1352-135insA	ENSP00000345739.3:n.1352-136_1352-135insA
ENST00000359526.8:c.1400-136_1400-135insA	ENSP00000352516.3:n.1400-136_1400-135insA
ENST00000540357.5:c.344-136_344-135insA	ENSP00000440457.2:n.344-136_344-135insA
ENST00000585843.1:n.557-136_557-135insA
ENST00000592705.5:c.*1090-136_*1090-135insA	ENSP00000466657.1:n.*1090-136_*1090-135insA
NM_001130823.1:c.1400-136_1400-135insA , LRG_362t1:c.1400-136_1400-135insA	NP_001124295.1:n.1400-136_1400-135insA
NM_001379.2:c.1352-136_1352-135insA	NP_001370.1:n.1352-136_1352-135insA
XM_011527772.1:c.1400-136_1400-135insA	XP_011526074.1:n.1400-136_1400-135insA
XM_011527773.1:c.1352-136_1352-135insA	XP_011526075.1:n.1352-136_1352-135insA
XM_011527774.1:c.989-136_989-135insA	XP_011526076.1:n.989-136_989-135insA
NM_001130823.2:c.1400-136_1400-135insA	NP_001124295.1:n.1400-136_1400-135insA
NM_001318730.1:c.1352-136_1352-135insA	NP_001305659.1:n.1352-136_1352-135insA
NM_001318731.1:c.1037-136_1037-135insA	NP_001305660.1:n.1037-136_1037-135insA
NM_001379.3:c.1352-136_1352-135insA	NP_001370.1:n.1352-136_1352-135insA
NM_001130823.3:c.1400-136_1400-135insA MANE Select	NP_001124295.1:n.1400-136_1400-135insA
NM_001318730.2:c.1352-136_1352-135insA	NP_001305659.1:n.1352-136_1352-135insA
NM_001318731.2:c.1037-136_1037-135insA	NP_001305660.1:n.1037-136_1037-135insA
NM_001379.4:c.1352-136_1352-135insA	NP_001370.1:n.1352-136_1352-135insA