Canonical Allele Identifier: CA403938022

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267087T>A (hg19) ; chr19:g.10156411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156411T>A , CM000681.2:g.10156411T>A	GRCh38
NC_000019.9:g.10267087T>A , CM000681.1:g.10267087T>A	GRCh37
NC_000019.8:g.10128087T>A	NCBI36
NG_028016.3:g.79876A>T , LRG_362:g.79876A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1379A>T MANE Select	ENSP00000352516.3:p.Asp460Val
ENST00000676604.1:n.991A>T
ENST00000676610.1:c.1331A>T	ENSP00000504236.1:p.Asp444Val
ENST00000676820.1:n.1387A>T
ENST00000676868.1:n.2015A>T
ENST00000677013.1:c.*1021A>T	ENSP00000503135.1:n.*1021A>T
ENST00000677250.1:c.*451A>T	ENSP00000502894.1:n.*451A>T
ENST00000677616.1:c.1022A>T	ENSP00000503055.1:p.Asp341Val
ENST00000677634.1:c.1331A>T	ENSP00000504246.1:p.Asp444Val
ENST00000677685.1:c.*556A>T	ENSP00000503407.1:n.*556A>T
ENST00000677783.1:n.1801A>T
ENST00000677946.1:c.1331A>T	ENSP00000504202.1:p.Asp444Val
ENST00000678024.1:n.1474A>T
ENST00000678694.1:n.652A>T
ENST00000678804.1:c.1331A>T	ENSP00000503853.1:p.Asp444Val
ENST00000679103.1:c.1331A>T	ENSP00000503151.1:p.Asp444Val
ENST00000679313.1:c.1331A>T	ENSP00000504512.1:p.Asp444Val
ENST00000340748.8:c.1331A>T	ENSP00000345739.3:p.Asp444Val
ENST00000359526.8:c.1379A>T	ENSP00000352516.3:p.Asp460Val
ENST00000540357.5:c.323A>T	ENSP00000440457.2:p.Asp108Val
ENST00000585843.1:n.536A>T
ENST00000592705.5:c.*1069A>T	ENSP00000466657.1:n.*1069A>T
NM_001130823.1:c.1379A>T , LRG_362t1:c.1379A>T	NP_001124295.1:p.Asp460Val
NM_001379.2:c.1331A>T	NP_001370.1:p.Asp444Val
XM_011527772.1:c.1379A>T	XP_011526074.1:p.Asp460Val
XM_011527773.1:c.1331A>T	XP_011526075.1:p.Asp444Val
XM_011527774.1:c.968A>T	XP_011526076.1:p.Asp323Val
NM_001130823.2:c.1379A>T	NP_001124295.1:p.Asp460Val
NM_001318730.1:c.1331A>T	NP_001305659.1:p.Asp444Val
NM_001318731.1:c.1016A>T	NP_001305660.1:p.Asp339Val
NM_001379.3:c.1331A>T	NP_001370.1:p.Asp444Val
NM_001130823.3:c.1379A>T MANE Select	NP_001124295.1:p.Asp460Val
NM_001318730.2:c.1331A>T	NP_001305659.1:p.Asp444Val
NM_001318731.2:c.1016A>T	NP_001305660.1:p.Asp339Val
NM_001379.4:c.1331A>T	NP_001370.1:p.Asp444Val