Canonical Allele Identifier: CA631451777

Gene: DNMT1

Linked Data

• dbSNP Id: rs1289118396
• gnomAD v2: 19-10267294-CTTTT-C
• gnomAD v3: 19-10156618-CTTTT-C
• gnomAD v4: 19-10156618-CTTTT-C
• MyVariant Identifiers: chr19:g.10267295_10267298del (hg19) ; chr19:g.10156619_10156622del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156622_10156625del , CM000681.2:g.10156622_10156625del	GRCh38
NC_000019.9:g.10267298_10267301del , CM000681.1:g.10267298_10267301del	GRCh37
NC_000019.8:g.10128298_10128301del	NCBI36
NG_028016.3:g.79665_79668del , LRG_362:g.79665_79668del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1281-113_1281-110del MANE Select	ENSP00000352516.3:n.1281-113_1281-110del
ENST00000676604.1:n.893-113_893-110del
ENST00000676610.1:c.1233-113_1233-110del	ENSP00000504236.1:n.1233-113_1233-110del
ENST00000676820.1:n.1289-113_1289-110del
ENST00000676868.1:n.1917-113_1917-110del
ENST00000677013.1:c.*923-113_*923-110del	ENSP00000503135.1:n.*923-113_*923-110del
ENST00000677250.1:c.*353-113_*353-110del	ENSP00000502894.1:n.*353-113_*353-110del
ENST00000677616.1:c.924-113_924-110del	ENSP00000503055.1:n.924-113_924-110del
ENST00000677634.1:c.1233-113_1233-110del	ENSP00000504246.1:n.1233-113_1233-110del
ENST00000677685.1:c.*458-113_*458-110del	ENSP00000503407.1:n.*458-113_*458-110del
ENST00000677783.1:n.1703-113_1703-110del
ENST00000677946.1:c.1233-113_1233-110del	ENSP00000504202.1:n.1233-113_1233-110del
ENST00000678024.1:n.1376-113_1376-110del
ENST00000678694.1:n.554-113_554-110del
ENST00000678804.1:c.1233-113_1233-110del	ENSP00000503853.1:n.1233-113_1233-110del
ENST00000679103.1:c.1233-113_1233-110del	ENSP00000503151.1:n.1233-113_1233-110del
ENST00000679313.1:c.1233-113_1233-110del	ENSP00000504512.1:n.1233-113_1233-110del
ENST00000340748.8:c.1233-113_1233-110del	ENSP00000345739.3:n.1233-113_1233-110del
ENST00000359526.8:c.1281-113_1281-110del	ENSP00000352516.3:n.1281-113_1281-110del
ENST00000540357.5:c.225-113_225-110del	ENSP00000440457.2:n.225-113_225-110del
ENST00000585843.1:n.438-113_438-110del
ENST00000592705.5:c.*971-113_*971-110del	ENSP00000466657.1:n.*971-113_*971-110del
NM_001130823.1:c.1281-113_1281-110del , LRG_362t1:c.1281-113_1281-110del	NP_001124295.1:n.1281-113_1281-110del
NM_001379.2:c.1233-113_1233-110del	NP_001370.1:n.1233-113_1233-110del
XM_011527772.1:c.1281-113_1281-110del	XP_011526074.1:n.1281-113_1281-110del
XM_011527773.1:c.1233-113_1233-110del	XP_011526075.1:n.1233-113_1233-110del
XM_011527774.1:c.870-113_870-110del	XP_011526076.1:n.870-113_870-110del
NM_001130823.2:c.1281-113_1281-110del	NP_001124295.1:n.1281-113_1281-110del
NM_001318730.1:c.1233-113_1233-110del	NP_001305659.1:n.1233-113_1233-110del
NM_001318731.1:c.918-113_918-110del	NP_001305660.1:n.918-113_918-110del
NM_001379.3:c.1233-113_1233-110del	NP_001370.1:n.1233-113_1233-110del
NM_001130823.3:c.1281-113_1281-110del MANE Select	NP_001124295.1:n.1281-113_1281-110del
NM_001318730.2:c.1233-113_1233-110del	NP_001305659.1:n.1233-113_1233-110del
NM_001318731.2:c.918-113_918-110del	NP_001305660.1:n.918-113_918-110del
NM_001379.4:c.1233-113_1233-110del	NP_001370.1:n.1233-113_1233-110del