Canonical Allele Identifier: CA9187473

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10136169G>A , CM000681.2:g.10136169G>A	GRCh38
NC_000019.9:g.10246845G>A , CM000681.1:g.10246845G>A	GRCh37
NC_000019.8:g.10107845G>A	NCBI36
NG_028016.3:g.100118C>T , LRG_362:g.100118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.4608C>T MANE Select	ENSP00000352516.3:p.Asp1536=
ENST00000586667.2:n.2643C>T
ENST00000589351.6:n.3794C>T
ENST00000676604.1:n.4220C>T
ENST00000676610.1:c.4560C>T	ENSP00000504236.1:p.Asp1520=
ENST00000676820.1:n.5454C>T
ENST00000676868.1:n.5244C>T
ENST00000677013.1:c.*4250C>T	ENSP00000503135.1:n.*4250C>T
ENST00000677038.1:n.1156C>T
ENST00000677250.1:c.*3680C>T	ENSP00000502894.1:n.*3680C>T
ENST00000677616.1:c.*830C>T	ENSP00000503055.1:n.*830C>T
ENST00000677634.1:c.*1163C>T	ENSP00000504246.1:n.*1163C>T
ENST00000677685.1:c.*3785C>T	ENSP00000503407.1:n.*3785C>T
ENST00000677783.1:n.5868C>T
ENST00000677946.1:c.4560C>T	ENSP00000504202.1:p.Asp1520=
ENST00000678024.1:n.5541C>T
ENST00000678107.1:n.1603C>T
ENST00000678239.1:n.1461C>T
ENST00000678647.1:n.2702C>T
ENST00000678694.1:n.3881C>T
ENST00000678804.1:c.4569C>T	ENSP00000503853.1:p.Asp1523=
ENST00000678851.1:n.602C>T
ENST00000678957.1:n.2272C>T
ENST00000679100.1:n.2747C>T
ENST00000679103.1:c.4560C>T	ENSP00000503151.1:p.Asp1520=
ENST00000679313.1:c.4569C>T	ENSP00000504512.1:p.Asp1523=
ENST00000340748.8:c.4560C>T	ENSP00000345739.3:p.Asp1520=
ENST00000359526.8:c.4608C>T	ENSP00000352516.3:p.Asp1536=
ENST00000540357.5:c.3552C>T	ENSP00000440457.2:p.Asp1184=
ENST00000586588.5:n.2481C>T
ENST00000588913.5:c.887C>T
ENST00000592705.5:c.*4298C>T	ENSP00000466657.1:n.*4298C>T
NM_001130823.1:c.4608C>T , LRG_362t1:c.4608C>T	NP_001124295.1:p.Asp1536=
NM_001379.2:c.4560C>T	NP_001370.1:p.Asp1520=
XM_011527772.1:c.4617C>T	XP_011526074.1:p.Asp1539=
XM_011527773.1:c.4569C>T	XP_011526075.1:p.Asp1523=
XM_011527774.1:c.4206C>T	XP_011526076.1:p.Asp1402=
NM_001130823.2:c.4608C>T	NP_001124295.1:p.Asp1536=
NM_001318730.1:c.4569C>T	NP_001305659.1:p.Asp1523=
NM_001318731.1:c.4245C>T	NP_001305660.1:p.Asp1415=
NM_001379.3:c.4560C>T	NP_001370.1:p.Asp1520=
NM_001130823.3:c.4608C>T MANE Select	NP_001124295.1:p.Asp1536=
NM_001318730.2:c.4569C>T	NP_001305659.1:p.Asp1523=
NM_001318731.2:c.4245C>T	NP_001305660.1:p.Asp1415=
NM_001379.4:c.4560C>T	NP_001370.1:p.Asp1520=