Canonical Allele Identifier: CA403934300

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10265260A>T (hg19) ; chr19:g.10154584A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154584A>T , CM000681.2:g.10154584A>T	GRCh38
NC_000019.9:g.10265260A>T , CM000681.1:g.10265260A>T	GRCh37
NC_000019.8:g.10126260A>T	NCBI36
NG_028016.3:g.81703T>A , LRG_362:g.81703T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.1832+2T>A MANE Select	ENSP00000352516.3:n.1832+2T>A
ENST00000676604.1:n.1444+2T>A
ENST00000676610.1:c.1784+2T>A	ENSP00000504236.1:n.1784+2T>A
ENST00000676820.1:n.1840+2T>A
ENST00000676868.1:n.2468+2T>A
ENST00000677013.1:c.*1474+2T>A	ENSP00000503135.1:n.*1474+2T>A
ENST00000677250.1:c.*904+2T>A	ENSP00000502894.1:n.*904+2T>A
ENST00000677616.1:c.1475+2T>A	ENSP00000503055.1:n.1475+2T>A
ENST00000677634.1:c.1784+2T>A	ENSP00000504246.1:n.1784+2T>A
ENST00000677685.1:c.*1009+2T>A	ENSP00000503407.1:n.*1009+2T>A
ENST00000677783.1:n.2254+2T>A
ENST00000677946.1:c.1784+2T>A	ENSP00000504202.1:n.1784+2T>A
ENST00000678024.1:n.1927+2T>A
ENST00000678694.1:n.1105+2T>A
ENST00000678804.1:c.1784+2T>A	ENSP00000503853.1:n.1784+2T>A
ENST00000679103.1:c.1784+2T>A	ENSP00000503151.1:n.1784+2T>A
ENST00000679313.1:c.1784+2T>A	ENSP00000504512.1:n.1784+2T>A
ENST00000340748.8:c.1784+2T>A	ENSP00000345739.3:n.1784+2T>A
ENST00000359526.8:c.1832+2T>A	ENSP00000352516.3:n.1832+2T>A
ENST00000540357.5:c.776+2T>A	ENSP00000440457.2:n.776+2T>A
ENST00000586799.1:c.218+2T>A
ENST00000592705.5:c.*1522+2T>A	ENSP00000466657.1:n.*1522+2T>A
NM_001130823.1:c.1832+2T>A , LRG_362t1:c.1832+2T>A	NP_001124295.1:n.1832+2T>A
NM_001379.2:c.1784+2T>A	NP_001370.1:n.1784+2T>A
XM_011527772.1:c.1832+2T>A	XP_011526074.1:n.1832+2T>A
XM_011527773.1:c.1784+2T>A	XP_011526075.1:n.1784+2T>A
XM_011527774.1:c.1421+2T>A	XP_011526076.1:n.1421+2T>A
NM_001130823.2:c.1832+2T>A	NP_001124295.1:n.1832+2T>A
NM_001318730.1:c.1784+2T>A	NP_001305659.1:n.1784+2T>A
NM_001318731.1:c.1469+2T>A	NP_001305660.1:n.1469+2T>A
NM_001379.3:c.1784+2T>A	NP_001370.1:n.1784+2T>A
NM_001130823.3:c.1832+2T>A MANE Select	NP_001124295.1:n.1832+2T>A
NM_001318730.2:c.1784+2T>A	NP_001305659.1:n.1784+2T>A
NM_001318731.2:c.1469+2T>A	NP_001305660.1:n.1469+2T>A
NM_001379.4:c.1784+2T>A	NP_001370.1:n.1784+2T>A