Canonical Allele Identifier: CA505467527

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10291177A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10180501A>C , CM000681.2:g.10180501A>C	GRCh38
NC_000019.9:g.10291177A>C , CM000681.1:g.10291177A>C	GRCh37
NC_000019.8:g.10152177A>C	NCBI36
NG_028016.3:g.55786T>G , LRG_362:g.55786T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.294T>G MANE Select	ENSP00000352516.3:p.Ala98=
ENST00000676610.1:c.294T>G	ENSP00000504236.1:p.Ala98=
ENST00000676820.1:n.350T>G
ENST00000677013.1:c.254T>G	ENSP00000503135.1:p.Leu85Arg
ENST00000677250.1:c.294T>G	ENSP00000502894.1:p.Ala98=
ENST00000677616.1:c.-70T>G	ENSP00000503055.1:n.-70T>G
ENST00000677634.1:c.294T>G	ENSP00000504246.1:p.Ala98=
ENST00000677685.1:c.225+277T>G	ENSP00000503407.1:n.225+277T>G
ENST00000677946.1:c.294T>G	ENSP00000504202.1:p.Ala98=
ENST00000678804.1:c.294T>G	ENSP00000503853.1:p.Ala98=
ENST00000679103.1:c.294T>G	ENSP00000503151.1:p.Ala98=
ENST00000679313.1:c.294T>G	ENSP00000504512.1:p.Ala98=
ENST00000340748.8:c.294T>G	ENSP00000345739.3:p.Ala98=
ENST00000359526.8:c.294T>G	ENSP00000352516.3:p.Ala98=
ENST00000540357.5:c.-560-3137T>G	ENSP00000440457.2:n.-560-3137T>G
ENST00000586086.1:n.451T>G
ENST00000586800.5:c.-70T>G	ENSP00000465555.1:n.-70T>G
ENST00000586988.5:c.*122T>G	ENSP00000464958.1:n.*122T>G
ENST00000588118.5:c.459T>G	ENSP00000465223.1:p.Ala153=
ENST00000588952.5:c.-70T>G	ENSP00000467050.1:n.-70T>G
ENST00000592054.5:c.-70T>G	ENSP00000468359.1:n.-70T>G
ENST00000592342.5:c.-70T>G	ENSP00000465993.1:n.-70T>G
ENST00000592705.5:c.254T>G	ENSP00000466657.1:p.Leu85Arg
NM_001130823.1:c.294T>G , LRG_362t1:c.294T>G	NP_001124295.1:p.Ala98=
NM_001379.2:c.294T>G	NP_001370.1:p.Ala98=
XM_011527772.1:c.294T>G	XP_011526074.1:p.Ala98=
XM_011527773.1:c.294T>G	XP_011526075.1:p.Ala98=
XM_011527774.1:c.-70T>G	XP_011526076.1:n.-70T>G
NM_001130823.2:c.294T>G	NP_001124295.1:p.Ala98=
NM_001318730.1:c.294T>G	NP_001305659.1:p.Ala98=
NM_001318731.1:c.-70T>G	NP_001305660.1:n.-70T>G
NM_001379.3:c.294T>G	NP_001370.1:p.Ala98=
NM_001130823.3:c.294T>G MANE Select	NP_001124295.1:p.Ala98=
NM_001318730.2:c.294T>G	NP_001305659.1:p.Ala98=
NM_001318731.2:c.-70T>G	NP_001305660.1:n.-70T>G
NM_001379.4:c.294T>G	NP_001370.1:p.Ala98=