Canonical Allele Identifier: CA403976334

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257147C>A (hg19) ; chr19:g.10146471C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146471C>A , CM000681.2:g.10146471C>A	GRCh38
NC_000019.9:g.10257147C>A , CM000681.1:g.10257147C>A	GRCh37
NC_000019.8:g.10118147C>A	NCBI36
NG_028016.3:g.89816G>T , LRG_362:g.89816G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2774G>T MANE Select	ENSP00000352516.3:p.Arg925Met
ENST00000586667.2:n.809G>T
ENST00000676604.1:n.2386G>T
ENST00000676610.1:c.2726G>T	ENSP00000504236.1:p.Arg909Met
ENST00000676820.1:n.2782G>T
ENST00000676868.1:n.3410G>T
ENST00000677013.1:c.*2416G>T	ENSP00000503135.1:n.*2416G>T
ENST00000677250.1:c.*1846G>T	ENSP00000502894.1:n.*1846G>T
ENST00000677616.1:c.2417G>T	ENSP00000503055.1:p.Arg806Met
ENST00000677634.1:c.2726G>T	ENSP00000504246.1:p.Arg909Met
ENST00000677685.1:c.*1951G>T	ENSP00000503407.1:n.*1951G>T
ENST00000677783.1:n.3196G>T
ENST00000677946.1:c.2726G>T	ENSP00000504202.1:p.Arg909Met
ENST00000678024.1:n.2869G>T
ENST00000678647.1:n.859G>T
ENST00000678694.1:n.2047G>T
ENST00000678804.1:c.2726G>T	ENSP00000503853.1:p.Arg909Met
ENST00000679100.1:n.913G>T
ENST00000679103.1:c.2726G>T	ENSP00000503151.1:p.Arg909Met
ENST00000679313.1:c.2726G>T	ENSP00000504512.1:p.Arg909Met
ENST00000340748.8:c.2726G>T	ENSP00000345739.3:p.Arg909Met
ENST00000359526.8:c.2774G>T	ENSP00000352516.3:p.Arg925Met
ENST00000540357.5:c.1718G>T	ENSP00000440457.2:p.Arg573Met
ENST00000592705.5:c.*2464G>T	ENSP00000466657.1:n.*2464G>T
NM_001130823.1:c.2774G>T , LRG_362t1:c.2774G>T	NP_001124295.1:p.Arg925Met
NM_001379.2:c.2726G>T	NP_001370.1:p.Arg909Met
XM_011527772.1:c.2774G>T	XP_011526074.1:p.Arg925Met
XM_011527773.1:c.2726G>T	XP_011526075.1:p.Arg909Met
XM_011527774.1:c.2363G>T	XP_011526076.1:p.Arg788Met
NM_001130823.2:c.2774G>T	NP_001124295.1:p.Arg925Met
NM_001318730.1:c.2726G>T	NP_001305659.1:p.Arg909Met
NM_001318731.1:c.2411G>T	NP_001305660.1:p.Arg804Met
NM_001379.3:c.2726G>T	NP_001370.1:p.Arg909Met
NM_001130823.3:c.2774G>T MANE Select	NP_001124295.1:p.Arg925Met
NM_001318730.2:c.2726G>T	NP_001305659.1:p.Arg909Met
NM_001318731.2:c.2411G>T	NP_001305660.1:p.Arg804Met
NM_001379.4:c.2726G>T	NP_001370.1:p.Arg909Met