Canonical Allele Identifier: CA914299221

Gene: DNMT1

Linked Data

• dbSNP Id: rs1568236154
• gnomAD v2: 19-10267316-CAG-C
• gnomAD v3: 19-10156640-CAG-C
• gnomAD v4: 19-10156640-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156643_10156644del , CM000681.2:g.10156643_10156644del	GRCh38
NC_000019.9:g.10267319_10267320del , CM000681.1:g.10267319_10267320del	GRCh37
NC_000019.8:g.10128319_10128320del	NCBI36
NG_028016.3:g.79645_79646del , LRG_362:g.79645_79646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1281-133_1281-132del MANE Select	ENSP00000352516.3:n.1281-133_1281-132del
ENST00000676604.1:n.893-133_893-132del
ENST00000676610.1:c.1233-133_1233-132del	ENSP00000504236.1:n.1233-133_1233-132del
ENST00000676820.1:n.1289-133_1289-132del
ENST00000676868.1:n.1917-133_1917-132del
ENST00000677013.1:c.*923-133_*923-132del	ENSP00000503135.1:n.*923-133_*923-132del
ENST00000677250.1:c.*353-133_*353-132del	ENSP00000502894.1:n.*353-133_*353-132del
ENST00000677616.1:c.924-133_924-132del	ENSP00000503055.1:n.924-133_924-132del
ENST00000677634.1:c.1233-133_1233-132del	ENSP00000504246.1:n.1233-133_1233-132del
ENST00000677685.1:c.*458-133_*458-132del	ENSP00000503407.1:n.*458-133_*458-132del
ENST00000677783.1:n.1703-133_1703-132del
ENST00000677946.1:c.1233-133_1233-132del	ENSP00000504202.1:n.1233-133_1233-132del
ENST00000678024.1:n.1376-133_1376-132del
ENST00000678694.1:n.554-133_554-132del
ENST00000678804.1:c.1233-133_1233-132del	ENSP00000503853.1:n.1233-133_1233-132del
ENST00000679103.1:c.1233-133_1233-132del	ENSP00000503151.1:n.1233-133_1233-132del
ENST00000679313.1:c.1233-133_1233-132del	ENSP00000504512.1:n.1233-133_1233-132del
ENST00000340748.8:c.1233-133_1233-132del	ENSP00000345739.3:n.1233-133_1233-132del
ENST00000359526.8:c.1281-133_1281-132del	ENSP00000352516.3:n.1281-133_1281-132del
ENST00000540357.5:c.225-133_225-132del	ENSP00000440457.2:n.225-133_225-132del
ENST00000585843.1:n.438-133_438-132del
ENST00000592705.5:c.*971-133_*971-132del	ENSP00000466657.1:n.*971-133_*971-132del
NM_001130823.1:c.1281-133_1281-132del , LRG_362t1:c.1281-133_1281-132del	NP_001124295.1:n.1281-133_1281-132del
NM_001379.2:c.1233-133_1233-132del	NP_001370.1:n.1233-133_1233-132del
XM_011527772.1:c.1281-133_1281-132del	XP_011526074.1:n.1281-133_1281-132del
XM_011527773.1:c.1233-133_1233-132del	XP_011526075.1:n.1233-133_1233-132del
XM_011527774.1:c.870-133_870-132del	XP_011526076.1:n.870-133_870-132del
NM_001130823.2:c.1281-133_1281-132del	NP_001124295.1:n.1281-133_1281-132del
NM_001318730.1:c.1233-133_1233-132del	NP_001305659.1:n.1233-133_1233-132del
NM_001318731.1:c.918-133_918-132del	NP_001305660.1:n.918-133_918-132del
NM_001379.3:c.1233-133_1233-132del	NP_001370.1:n.1233-133_1233-132del
NM_001130823.3:c.1281-133_1281-132del MANE Select	NP_001124295.1:n.1281-133_1281-132del
NM_001318730.2:c.1233-133_1233-132del	NP_001305659.1:n.1233-133_1233-132del
NM_001318731.2:c.918-133_918-132del	NP_001305660.1:n.918-133_918-132del
NM_001379.4:c.1233-133_1233-132del	NP_001370.1:n.1233-133_1233-132del