Canonical Allele Identifier: CA505346781

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10156428-T-G
• MyVariant Identifiers: chr19:g.10267104T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156428T>G , CM000681.2:g.10156428T>G	GRCh38
NC_000019.9:g.10267104T>G , CM000681.1:g.10267104T>G	GRCh37
NC_000019.8:g.10128104T>G	NCBI36
NG_028016.3:g.79859A>C , LRG_362:g.79859A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1362A>C MANE Select	ENSP00000352516.3:p.Ser454=
ENST00000676604.1:n.974A>C
ENST00000676610.1:c.1314A>C	ENSP00000504236.1:p.Ser438=
ENST00000676820.1:n.1370A>C
ENST00000676868.1:n.1998A>C
ENST00000677013.1:c.*1004A>C	ENSP00000503135.1:n.*1004A>C
ENST00000677250.1:c.*434A>C	ENSP00000502894.1:n.*434A>C
ENST00000677616.1:c.1005A>C	ENSP00000503055.1:p.Ser335=
ENST00000677634.1:c.1314A>C	ENSP00000504246.1:p.Ser438=
ENST00000677685.1:c.*539A>C	ENSP00000503407.1:n.*539A>C
ENST00000677783.1:n.1784A>C
ENST00000677946.1:c.1314A>C	ENSP00000504202.1:p.Ser438=
ENST00000678024.1:n.1457A>C
ENST00000678694.1:n.635A>C
ENST00000678804.1:c.1314A>C	ENSP00000503853.1:p.Ser438=
ENST00000679103.1:c.1314A>C	ENSP00000503151.1:p.Ser438=
ENST00000679313.1:c.1314A>C	ENSP00000504512.1:p.Ser438=
ENST00000340748.8:c.1314A>C	ENSP00000345739.3:p.Ser438=
ENST00000359526.8:c.1362A>C	ENSP00000352516.3:p.Ser454=
ENST00000540357.5:c.306A>C	ENSP00000440457.2:p.Ser102=
ENST00000585843.1:n.519A>C
ENST00000592705.5:c.*1052A>C	ENSP00000466657.1:n.*1052A>C
NM_001130823.1:c.1362A>C , LRG_362t1:c.1362A>C	NP_001124295.1:p.Ser454=
NM_001379.2:c.1314A>C	NP_001370.1:p.Ser438=
XM_011527772.1:c.1362A>C	XP_011526074.1:p.Ser454=
XM_011527773.1:c.1314A>C	XP_011526075.1:p.Ser438=
XM_011527774.1:c.951A>C	XP_011526076.1:p.Ser317=
NM_001130823.2:c.1362A>C	NP_001124295.1:p.Ser454=
NM_001318730.1:c.1314A>C	NP_001305659.1:p.Ser438=
NM_001318731.1:c.999A>C	NP_001305660.1:p.Ser333=
NM_001379.3:c.1314A>C	NP_001370.1:p.Ser438=
NM_001130823.3:c.1362A>C MANE Select	NP_001124295.1:p.Ser454=
NM_001318730.2:c.1314A>C	NP_001305659.1:p.Ser438=
NM_001318731.2:c.999A>C	NP_001305660.1:p.Ser333=
NM_001379.4:c.1314A>C	NP_001370.1:p.Ser438=