Canonical Allele Identifier: CA9187381

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10134221G>A , CM000681.2:g.10134221G>A	GRCh38
NC_000019.9:g.10244897G>A , CM000681.1:g.10244897G>A	GRCh37
NC_000019.8:g.10105897G>A	NCBI36
NG_028016.3:g.102066C>T , LRG_362:g.102066C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.4860C>T MANE Select	ENSP00000352516.3:p.Ala1620=
ENST00000586667.2:n.2895C>T
ENST00000589351.6:n.4046C>T
ENST00000676604.1:n.4472C>T
ENST00000676610.1:c.*1398C>T	ENSP00000504236.1:n.*1398C>T
ENST00000676820.1:n.5706C>T
ENST00000676868.1:n.5496C>T
ENST00000677013.1:c.*4502C>T	ENSP00000503135.1:n.*4502C>T
ENST00000677038.1:n.1408C>T
ENST00000677135.1:n.341C>T
ENST00000677250.1:c.*3932C>T	ENSP00000502894.1:n.*3932C>T
ENST00000677616.1:c.*1082C>T	ENSP00000503055.1:n.*1082C>T
ENST00000677634.1:c.*1415C>T	ENSP00000504246.1:n.*1415C>T
ENST00000677685.1:c.*4037C>T	ENSP00000503407.1:n.*4037C>T
ENST00000677783.1:n.6120C>T
ENST00000677946.1:c.4812C>T	ENSP00000504202.1:p.Ala1604=
ENST00000678024.1:n.5793C>T
ENST00000678107.1:n.1855C>T
ENST00000678647.1:n.2954C>T
ENST00000678694.1:n.4133C>T
ENST00000678804.1:c.4821C>T	ENSP00000503853.1:p.Ala1607=
ENST00000678851.1:n.2282C>T
ENST00000678957.1:n.2524C>T
ENST00000679100.1:n.2999C>T
ENST00000679103.1:c.4726-520C>T	ENSP00000503151.1:n.4726-520C>T
ENST00000679313.1:c.4735-520C>T	ENSP00000504512.1:n.4735-520C>T
ENST00000340748.8:c.4812C>T	ENSP00000345739.3:p.Ala1604=
ENST00000359526.8:c.4860C>T	ENSP00000352516.3:p.Ala1620=
ENST00000540357.5:c.3804C>T	ENSP00000440457.2:p.Ala1268=
ENST00000586588.5:n.2733C>T
ENST00000588913.5:c.1436C>T
ENST00000591798.5:n.166C>T
ENST00000592705.5:c.*4550C>T	ENSP00000466657.1:n.*4550C>T
NM_001130823.1:c.4860C>T , LRG_362t1:c.4860C>T	NP_001124295.1:p.Ala1620=
NM_001379.2:c.4812C>T	NP_001370.1:p.Ala1604=
XM_011527772.1:c.4869C>T	XP_011526074.1:p.Ala1623=
XM_011527773.1:c.4821C>T	XP_011526075.1:p.Ala1607=
XM_011527774.1:c.4458C>T	XP_011526076.1:p.Ala1486=
NM_001130823.2:c.4860C>T	NP_001124295.1:p.Ala1620=
NM_001318730.1:c.4821C>T	NP_001305659.1:p.Ala1607=
NM_001318731.1:c.4497C>T	NP_001305660.1:p.Ala1499=
NM_001379.3:c.4812C>T	NP_001370.1:p.Ala1604=
NM_001130823.3:c.4860C>T MANE Select	NP_001124295.1:p.Ala1620=
NM_001318730.2:c.4821C>T	NP_001305659.1:p.Ala1607=
NM_001318731.2:c.4497C>T	NP_001305660.1:p.Ala1499=
NM_001379.4:c.4812C>T	NP_001370.1:p.Ala1604=