Canonical Allele Identifier: CA2322290413

Gene: DNMT1

Linked Data

• dbSNP Id: rs2038462657
• gnomAD v3: 19-10156616-CTCT-C
• gnomAD v4: 19-10156616-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156618_10156620del , CM000681.2:g.10156618_10156620del	GRCh38
NC_000019.9:g.10267294_10267296del , CM000681.1:g.10267294_10267296del	GRCh37
NC_000019.8:g.10128294_10128296del	NCBI36
NG_028016.3:g.79668_79670del , LRG_362:g.79668_79670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1281-110_1281-108del MANE Select	ENSP00000352516.3:n.1281-110_1281-108del
ENST00000676604.1:n.893-110_893-108del
ENST00000676610.1:c.1233-110_1233-108del	ENSP00000504236.1:n.1233-110_1233-108del
ENST00000676820.1:n.1289-110_1289-108del
ENST00000676868.1:n.1917-110_1917-108del
ENST00000677013.1:c.*923-110_*923-108del	ENSP00000503135.1:n.*923-110_*923-108del
ENST00000677250.1:c.*353-110_*353-108del	ENSP00000502894.1:n.*353-110_*353-108del
ENST00000677616.1:c.924-110_924-108del	ENSP00000503055.1:n.924-110_924-108del
ENST00000677634.1:c.1233-110_1233-108del	ENSP00000504246.1:n.1233-110_1233-108del
ENST00000677685.1:c.*458-110_*458-108del	ENSP00000503407.1:n.*458-110_*458-108del
ENST00000677783.1:n.1703-110_1703-108del
ENST00000677946.1:c.1233-110_1233-108del	ENSP00000504202.1:n.1233-110_1233-108del
ENST00000678024.1:n.1376-110_1376-108del
ENST00000678694.1:n.554-110_554-108del
ENST00000678804.1:c.1233-110_1233-108del	ENSP00000503853.1:n.1233-110_1233-108del
ENST00000679103.1:c.1233-110_1233-108del	ENSP00000503151.1:n.1233-110_1233-108del
ENST00000679313.1:c.1233-110_1233-108del	ENSP00000504512.1:n.1233-110_1233-108del
ENST00000340748.8:c.1233-110_1233-108del	ENSP00000345739.3:n.1233-110_1233-108del
ENST00000359526.8:c.1281-110_1281-108del	ENSP00000352516.3:n.1281-110_1281-108del
ENST00000540357.5:c.225-110_225-108del	ENSP00000440457.2:n.225-110_225-108del
ENST00000585843.1:n.438-110_438-108del
ENST00000592705.5:c.*971-110_*971-108del	ENSP00000466657.1:n.*971-110_*971-108del
NM_001130823.1:c.1281-110_1281-108del , LRG_362t1:c.1281-110_1281-108del	NP_001124295.1:n.1281-110_1281-108del
NM_001379.2:c.1233-110_1233-108del	NP_001370.1:n.1233-110_1233-108del
XM_011527772.1:c.1281-110_1281-108del	XP_011526074.1:n.1281-110_1281-108del
XM_011527773.1:c.1233-110_1233-108del	XP_011526075.1:n.1233-110_1233-108del
XM_011527774.1:c.870-110_870-108del	XP_011526076.1:n.870-110_870-108del
NM_001130823.2:c.1281-110_1281-108del	NP_001124295.1:n.1281-110_1281-108del
NM_001318730.1:c.1233-110_1233-108del	NP_001305659.1:n.1233-110_1233-108del
NM_001318731.1:c.918-110_918-108del	NP_001305660.1:n.918-110_918-108del
NM_001379.3:c.1233-110_1233-108del	NP_001370.1:n.1233-110_1233-108del
NM_001130823.3:c.1281-110_1281-108del MANE Select	NP_001124295.1:n.1281-110_1281-108del
NM_001318730.2:c.1233-110_1233-108del	NP_001305659.1:n.1233-110_1233-108del
NM_001318731.2:c.918-110_918-108del	NP_001305660.1:n.918-110_918-108del
NM_001379.4:c.1233-110_1233-108del	NP_001370.1:n.1233-110_1233-108del