Canonical Allele Identifier: CA505346754

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267086A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156410A>G , CM000681.2:g.10156410A>G	GRCh38
NC_000019.9:g.10267086A>G , CM000681.1:g.10267086A>G	GRCh37
NC_000019.8:g.10128086A>G	NCBI36
NG_028016.3:g.79877T>C , LRG_362:g.79877T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1380T>C MANE Select	ENSP00000352516.3:p.Asp460=
ENST00000676604.1:n.992T>C
ENST00000676610.1:c.1332T>C	ENSP00000504236.1:p.Asp444=
ENST00000676820.1:n.1388T>C
ENST00000676868.1:n.2016T>C
ENST00000677013.1:c.*1022T>C	ENSP00000503135.1:n.*1022T>C
ENST00000677250.1:c.*452T>C	ENSP00000502894.1:n.*452T>C
ENST00000677616.1:c.1023T>C	ENSP00000503055.1:p.Asp341=
ENST00000677634.1:c.1332T>C	ENSP00000504246.1:p.Asp444=
ENST00000677685.1:c.*557T>C	ENSP00000503407.1:n.*557T>C
ENST00000677783.1:n.1802T>C
ENST00000677946.1:c.1332T>C	ENSP00000504202.1:p.Asp444=
ENST00000678024.1:n.1475T>C
ENST00000678694.1:n.653T>C
ENST00000678804.1:c.1332T>C	ENSP00000503853.1:p.Asp444=
ENST00000679103.1:c.1332T>C	ENSP00000503151.1:p.Asp444=
ENST00000679313.1:c.1332T>C	ENSP00000504512.1:p.Asp444=
ENST00000340748.8:c.1332T>C	ENSP00000345739.3:p.Asp444=
ENST00000359526.8:c.1380T>C	ENSP00000352516.3:p.Asp460=
ENST00000540357.5:c.324T>C	ENSP00000440457.2:p.Asp108=
ENST00000585843.1:n.537T>C
ENST00000592705.5:c.*1070T>C	ENSP00000466657.1:n.*1070T>C
NM_001130823.1:c.1380T>C , LRG_362t1:c.1380T>C	NP_001124295.1:p.Asp460=
NM_001379.2:c.1332T>C	NP_001370.1:p.Asp444=
XM_011527772.1:c.1380T>C	XP_011526074.1:p.Asp460=
XM_011527773.1:c.1332T>C	XP_011526075.1:p.Asp444=
XM_011527774.1:c.969T>C	XP_011526076.1:p.Asp323=
NM_001130823.2:c.1380T>C	NP_001124295.1:p.Asp460=
NM_001318730.1:c.1332T>C	NP_001305659.1:p.Asp444=
NM_001318731.1:c.1017T>C	NP_001305660.1:p.Asp339=
NM_001379.3:c.1332T>C	NP_001370.1:p.Asp444=
NM_001130823.3:c.1380T>C MANE Select	NP_001124295.1:p.Asp460=
NM_001318730.2:c.1332T>C	NP_001305659.1:p.Asp444=
NM_001318731.2:c.1017T>C	NP_001305660.1:p.Asp339=
NM_001379.4:c.1332T>C	NP_001370.1:p.Asp444=