Canonical Allele Identifier: CA2588330556

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10156622-TTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156630_10156633del , CM000681.2:g.10156630_10156633del	GRCh38
NC_000019.9:g.10267306_10267309del , CM000681.1:g.10267306_10267309del	GRCh37
NC_000019.8:g.10128306_10128309del	NCBI36
NG_028016.3:g.79661_79664del , LRG_362:g.79661_79664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1281-117_1281-114del MANE Select	ENSP00000352516.3:n.1281-117_1281-114del
ENST00000676604.1:n.893-117_893-114del
ENST00000676610.1:c.1233-117_1233-114del	ENSP00000504236.1:n.1233-117_1233-114del
ENST00000676820.1:n.1289-117_1289-114del
ENST00000676868.1:n.1917-117_1917-114del
ENST00000677013.1:c.*923-117_*923-114del	ENSP00000503135.1:n.*923-117_*923-114del
ENST00000677250.1:c.*353-117_*353-114del	ENSP00000502894.1:n.*353-117_*353-114del
ENST00000677616.1:c.924-117_924-114del	ENSP00000503055.1:n.924-117_924-114del
ENST00000677634.1:c.1233-117_1233-114del	ENSP00000504246.1:n.1233-117_1233-114del
ENST00000677685.1:c.*458-117_*458-114del	ENSP00000503407.1:n.*458-117_*458-114del
ENST00000677783.1:n.1703-117_1703-114del
ENST00000677946.1:c.1233-117_1233-114del	ENSP00000504202.1:n.1233-117_1233-114del
ENST00000678024.1:n.1376-117_1376-114del
ENST00000678694.1:n.554-117_554-114del
ENST00000678804.1:c.1233-117_1233-114del	ENSP00000503853.1:n.1233-117_1233-114del
ENST00000679103.1:c.1233-117_1233-114del	ENSP00000503151.1:n.1233-117_1233-114del
ENST00000679313.1:c.1233-117_1233-114del	ENSP00000504512.1:n.1233-117_1233-114del
ENST00000340748.8:c.1233-117_1233-114del	ENSP00000345739.3:n.1233-117_1233-114del
ENST00000359526.8:c.1281-117_1281-114del	ENSP00000352516.3:n.1281-117_1281-114del
ENST00000540357.5:c.225-117_225-114del	ENSP00000440457.2:n.225-117_225-114del
ENST00000585843.1:n.438-117_438-114del
ENST00000592705.5:c.*971-117_*971-114del	ENSP00000466657.1:n.*971-117_*971-114del
NM_001130823.1:c.1281-117_1281-114del , LRG_362t1:c.1281-117_1281-114del	NP_001124295.1:n.1281-117_1281-114del
NM_001379.2:c.1233-117_1233-114del	NP_001370.1:n.1233-117_1233-114del
XM_011527772.1:c.1281-117_1281-114del	XP_011526074.1:n.1281-117_1281-114del
XM_011527773.1:c.1233-117_1233-114del	XP_011526075.1:n.1233-117_1233-114del
XM_011527774.1:c.870-117_870-114del	XP_011526076.1:n.870-117_870-114del
NM_001130823.2:c.1281-117_1281-114del	NP_001124295.1:n.1281-117_1281-114del
NM_001318730.1:c.1233-117_1233-114del	NP_001305659.1:n.1233-117_1233-114del
NM_001318731.1:c.918-117_918-114del	NP_001305660.1:n.918-117_918-114del
NM_001379.3:c.1233-117_1233-114del	NP_001370.1:n.1233-117_1233-114del
NM_001130823.3:c.1281-117_1281-114del MANE Select	NP_001124295.1:n.1281-117_1281-114del
NM_001318730.2:c.1233-117_1233-114del	NP_001305659.1:n.1233-117_1233-114del
NM_001318731.2:c.918-117_918-114del	NP_001305660.1:n.918-117_918-114del
NM_001379.4:c.1233-117_1233-114del	NP_001370.1:n.1233-117_1233-114del