Canonical Allele Identifier: CA403938306

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267159C>T (hg19) ; chr19:g.10156483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156483C>T , CM000681.2:g.10156483C>T	GRCh38
NC_000019.9:g.10267159C>T , CM000681.1:g.10267159C>T	GRCh37
NC_000019.8:g.10128159C>T	NCBI36
NG_028016.3:g.79804G>A , LRG_362:g.79804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1307G>A MANE Select	ENSP00000352516.3:p.Cys436Tyr
ENST00000676604.1:n.919G>A
ENST00000676610.1:c.1259G>A	ENSP00000504236.1:p.Cys420Tyr
ENST00000676820.1:n.1315G>A
ENST00000676868.1:n.1943G>A
ENST00000677013.1:c.*949G>A	ENSP00000503135.1:n.*949G>A
ENST00000677250.1:c.*379G>A	ENSP00000502894.1:n.*379G>A
ENST00000677616.1:c.950G>A	ENSP00000503055.1:p.Cys317Tyr
ENST00000677634.1:c.1259G>A	ENSP00000504246.1:p.Cys420Tyr
ENST00000677685.1:c.*484G>A	ENSP00000503407.1:n.*484G>A
ENST00000677783.1:n.1729G>A
ENST00000677946.1:c.1259G>A	ENSP00000504202.1:p.Cys420Tyr
ENST00000678024.1:n.1402G>A
ENST00000678694.1:n.580G>A
ENST00000678804.1:c.1259G>A	ENSP00000503853.1:p.Cys420Tyr
ENST00000679103.1:c.1259G>A	ENSP00000503151.1:p.Cys420Tyr
ENST00000679313.1:c.1259G>A	ENSP00000504512.1:p.Cys420Tyr
ENST00000340748.8:c.1259G>A	ENSP00000345739.3:p.Cys420Tyr
ENST00000359526.8:c.1307G>A	ENSP00000352516.3:p.Cys436Tyr
ENST00000540357.5:c.251G>A	ENSP00000440457.2:p.Cys84Tyr
ENST00000585843.1:n.464G>A
ENST00000592705.5:c.*997G>A	ENSP00000466657.1:n.*997G>A
NM_001130823.1:c.1307G>A , LRG_362t1:c.1307G>A	NP_001124295.1:p.Cys436Tyr
NM_001379.2:c.1259G>A	NP_001370.1:p.Cys420Tyr
XM_011527772.1:c.1307G>A	XP_011526074.1:p.Cys436Tyr
XM_011527773.1:c.1259G>A	XP_011526075.1:p.Cys420Tyr
XM_011527774.1:c.896G>A	XP_011526076.1:p.Cys299Tyr
NM_001130823.2:c.1307G>A	NP_001124295.1:p.Cys436Tyr
NM_001318730.1:c.1259G>A	NP_001305659.1:p.Cys420Tyr
NM_001318731.1:c.944G>A	NP_001305660.1:p.Cys315Tyr
NM_001379.3:c.1259G>A	NP_001370.1:p.Cys420Tyr
NM_001130823.3:c.1307G>A MANE Select	NP_001124295.1:p.Cys436Tyr
NM_001318730.2:c.1259G>A	NP_001305659.1:p.Cys420Tyr
NM_001318731.2:c.944G>A	NP_001305660.1:p.Cys315Tyr
NM_001379.4:c.1259G>A	NP_001370.1:p.Cys420Tyr