Canonical Allele Identifier: CA993429675

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149834C>T , CM000681.2:g.10149834C>T	GRCh38
NC_000019.9:g.10260510C>T , CM000681.1:g.10260510C>T	GRCh37
NC_000019.8:g.10121510C>T	NCBI36
NG_028016.3:g.86453G>A , LRG_362:g.86453G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2381+19G>A MANE Select	ENSP00000352516.3:n.2381+19G>A
ENST00000586667.2:n.416+19G>A
ENST00000676604.1:n.1993+19G>A
ENST00000676610.1:c.2333+19G>A	ENSP00000504236.1:n.2333+19G>A
ENST00000676820.1:n.2389+19G>A
ENST00000676868.1:n.3017+19G>A
ENST00000677013.1:c.*2023+19G>A	ENSP00000503135.1:n.*2023+19G>A
ENST00000677250.1:c.*1453+19G>A	ENSP00000502894.1:n.*1453+19G>A
ENST00000677616.1:c.2024+19G>A	ENSP00000503055.1:n.2024+19G>A
ENST00000677634.1:c.2333+19G>A	ENSP00000504246.1:n.2333+19G>A
ENST00000677685.1:c.*1558+19G>A	ENSP00000503407.1:n.*1558+19G>A
ENST00000677783.1:n.2803+19G>A
ENST00000677946.1:c.2333+19G>A	ENSP00000504202.1:n.2333+19G>A
ENST00000678024.1:n.2476+19G>A
ENST00000678647.1:n.466+19G>A
ENST00000678694.1:n.1654+19G>A
ENST00000678804.1:c.2333+19G>A	ENSP00000503853.1:n.2333+19G>A
ENST00000679100.1:n.520+19G>A
ENST00000679103.1:c.2333+19G>A	ENSP00000503151.1:n.2333+19G>A
ENST00000679313.1:c.2333+19G>A	ENSP00000504512.1:n.2333+19G>A
ENST00000340748.8:c.2333+19G>A	ENSP00000345739.3:n.2333+19G>A
ENST00000359526.8:c.2381+19G>A	ENSP00000352516.3:n.2381+19G>A
ENST00000540357.5:c.1325+19G>A	ENSP00000440457.2:n.1325+19G>A
ENST00000586667.1:n.416+19G>A
ENST00000592705.5:c.*2071+19G>A	ENSP00000466657.1:n.*2071+19G>A
NM_001130823.1:c.2381+19G>A , LRG_362t1:c.2381+19G>A	NP_001124295.1:n.2381+19G>A
NM_001379.2:c.2333+19G>A	NP_001370.1:n.2333+19G>A
XM_011527772.1:c.2381+19G>A	XP_011526074.1:n.2381+19G>A
XM_011527773.1:c.2333+19G>A	XP_011526075.1:n.2333+19G>A
XM_011527774.1:c.1970+19G>A	XP_011526076.1:n.1970+19G>A
NM_001130823.2:c.2381+19G>A	NP_001124295.1:n.2381+19G>A
NM_001318730.1:c.2333+19G>A	NP_001305659.1:n.2333+19G>A
NM_001318731.1:c.2018+19G>A	NP_001305660.1:n.2018+19G>A
NM_001379.3:c.2333+19G>A	NP_001370.1:n.2333+19G>A
NM_001130823.3:c.2381+19G>A MANE Select	NP_001124295.1:n.2381+19G>A
NM_001318730.2:c.2333+19G>A	NP_001305659.1:n.2333+19G>A
NM_001318731.2:c.2018+19G>A	NP_001305660.1:n.2018+19G>A
NM_001379.4:c.2333+19G>A	NP_001370.1:n.2333+19G>A