Canonical Allele Identifier: CA2843065238

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146480dup , CM000681.2:g.10146480dup	GRCh38
NC_000019.9:g.10257156dup , CM000681.1:g.10257156dup	GRCh37
NC_000019.8:g.10118156dup	NCBI36
NG_028016.3:g.89809dup , LRG_362:g.89809dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2767dup MANE Select	ENSP00000352516.3:p.Ile923AsnfsTer13
ENST00000586667.2:n.802dup
ENST00000676604.1:n.2379dup
ENST00000676610.1:c.2719dup	ENSP00000504236.1:p.Ile907AsnfsTer13
ENST00000676820.1:n.2775dup
ENST00000676868.1:n.3403dup
ENST00000677013.1:c.*2409dup	ENSP00000503135.1:n.*2409dup
ENST00000677250.1:c.*1839dup	ENSP00000502894.1:n.*1839dup
ENST00000677616.1:c.2410dup	ENSP00000503055.1:p.Ile804AsnfsTer13
ENST00000677634.1:c.2719dup	ENSP00000504246.1:p.Ile907AsnfsTer13
ENST00000677685.1:c.*1944dup	ENSP00000503407.1:n.*1944dup
ENST00000677783.1:n.3189dup
ENST00000677946.1:c.2719dup	ENSP00000504202.1:p.Ile907AsnfsTer13
ENST00000678024.1:n.2862dup
ENST00000678647.1:n.852dup
ENST00000678694.1:n.2040dup
ENST00000678804.1:c.2719dup	ENSP00000503853.1:p.Ile907AsnfsTer13
ENST00000679100.1:n.906dup
ENST00000679103.1:c.2719dup	ENSP00000503151.1:p.Ile907AsnfsTer13
ENST00000679313.1:c.2719dup	ENSP00000504512.1:p.Ile907AsnfsTer13
ENST00000340748.8:c.2719dup	ENSP00000345739.3:p.Ile907AsnfsTer13
ENST00000359526.8:c.2767dup	ENSP00000352516.3:p.Ile923AsnfsTer13
ENST00000540357.5:c.1711dup	ENSP00000440457.2:p.Ile571AsnfsTer13
ENST00000592705.5:c.*2457dup	ENSP00000466657.1:n.*2457dup
NM_001130823.1:c.2767dup , LRG_362t1:c.2767dup	NP_001124295.1:p.Ile923AsnfsTer13
NM_001379.2:c.2719dup	NP_001370.1:p.Ile907AsnfsTer13
XM_011527772.1:c.2767dup	XP_011526074.1:p.Ile923AsnfsTer13
XM_011527773.1:c.2719dup	XP_011526075.1:p.Ile907AsnfsTer13
XM_011527774.1:c.2356dup	XP_011526076.1:p.Ile786AsnfsTer13
NM_001130823.2:c.2767dup	NP_001124295.1:p.Ile923AsnfsTer13
NM_001318730.1:c.2719dup	NP_001305659.1:p.Ile907AsnfsTer13
NM_001318731.1:c.2404dup	NP_001305660.1:p.Ile802AsnfsTer13
NM_001379.3:c.2719dup	NP_001370.1:p.Ile907AsnfsTer13
NM_001130823.3:c.2767dup MANE Select	NP_001124295.1:p.Ile923AsnfsTer13
NM_001318730.2:c.2719dup	NP_001305659.1:p.Ile907AsnfsTer13
NM_001318731.2:c.2404dup	NP_001305660.1:p.Ile802AsnfsTer13
NM_001379.4:c.2719dup	NP_001370.1:p.Ile907AsnfsTer13