Canonical Allele Identifier: CA403938197

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267129T>A (hg19) ; chr19:g.10156453T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156453T>A , CM000681.2:g.10156453T>A	GRCh38
NC_000019.9:g.10267129T>A , CM000681.1:g.10267129T>A	GRCh37
NC_000019.8:g.10128129T>A	NCBI36
NG_028016.3:g.79834A>T , LRG_362:g.79834A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1337A>T MANE Select	ENSP00000352516.3:p.Asn446Ile
ENST00000676604.1:n.949A>T
ENST00000676610.1:c.1289A>T	ENSP00000504236.1:p.Asn430Ile
ENST00000676820.1:n.1345A>T
ENST00000676868.1:n.1973A>T
ENST00000677013.1:c.*979A>T	ENSP00000503135.1:n.*979A>T
ENST00000677250.1:c.*409A>T	ENSP00000502894.1:n.*409A>T
ENST00000677616.1:c.980A>T	ENSP00000503055.1:p.Asn327Ile
ENST00000677634.1:c.1289A>T	ENSP00000504246.1:p.Asn430Ile
ENST00000677685.1:c.*514A>T	ENSP00000503407.1:n.*514A>T
ENST00000677783.1:n.1759A>T
ENST00000677946.1:c.1289A>T	ENSP00000504202.1:p.Asn430Ile
ENST00000678024.1:n.1432A>T
ENST00000678694.1:n.610A>T
ENST00000678804.1:c.1289A>T	ENSP00000503853.1:p.Asn430Ile
ENST00000679103.1:c.1289A>T	ENSP00000503151.1:p.Asn430Ile
ENST00000679313.1:c.1289A>T	ENSP00000504512.1:p.Asn430Ile
ENST00000340748.8:c.1289A>T	ENSP00000345739.3:p.Asn430Ile
ENST00000359526.8:c.1337A>T	ENSP00000352516.3:p.Asn446Ile
ENST00000540357.5:c.281A>T	ENSP00000440457.2:p.Asn94Ile
ENST00000585843.1:n.494A>T
ENST00000592705.5:c.*1027A>T	ENSP00000466657.1:n.*1027A>T
NM_001130823.1:c.1337A>T , LRG_362t1:c.1337A>T	NP_001124295.1:p.Asn446Ile
NM_001379.2:c.1289A>T	NP_001370.1:p.Asn430Ile
XM_011527772.1:c.1337A>T	XP_011526074.1:p.Asn446Ile
XM_011527773.1:c.1289A>T	XP_011526075.1:p.Asn430Ile
XM_011527774.1:c.926A>T	XP_011526076.1:p.Asn309Ile
NM_001130823.2:c.1337A>T	NP_001124295.1:p.Asn446Ile
NM_001318730.1:c.1289A>T	NP_001305659.1:p.Asn430Ile
NM_001318731.1:c.974A>T	NP_001305660.1:p.Asn325Ile
NM_001379.3:c.1289A>T	NP_001370.1:p.Asn430Ile
NM_001130823.3:c.1337A>T MANE Select	NP_001124295.1:p.Asn446Ile
NM_001318730.2:c.1289A>T	NP_001305659.1:p.Asn430Ile
NM_001318731.2:c.974A>T	NP_001305660.1:p.Asn325Ile
NM_001379.4:c.1289A>T	NP_001370.1:p.Asn430Ile