Canonical Allele Identifier: CA631709540

Gene: DNMT1

Linked Data

• dbSNP Id: rs1263806852
• gnomAD v2: 19-10257250-T-C
• gnomAD v4: 19-10146574-T-C
• MyVariant Identifiers: chr19:g.10257250T>C (hg19) ; chr19:g.10146574T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146574T>C , CM000681.2:g.10146574T>C	GRCh38
NC_000019.9:g.10257250T>C , CM000681.1:g.10257250T>C	GRCh37
NC_000019.8:g.10118250T>C	NCBI36
NG_028016.3:g.89713A>G , LRG_362:g.89713A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2721-50A>G MANE Select	ENSP00000352516.3:n.2721-50A>G
ENST00000586667.2:n.756-50A>G
ENST00000676604.1:n.2333-50A>G
ENST00000676610.1:c.2673-50A>G	ENSP00000504236.1:n.2673-50A>G
ENST00000676820.1:n.2729-50A>G
ENST00000676868.1:n.3357-50A>G
ENST00000677013.1:c.*2363-50A>G	ENSP00000503135.1:n.*2363-50A>G
ENST00000677250.1:c.*1793-50A>G	ENSP00000502894.1:n.*1793-50A>G
ENST00000677616.1:c.2364-50A>G	ENSP00000503055.1:n.2364-50A>G
ENST00000677634.1:c.2673-50A>G	ENSP00000504246.1:n.2673-50A>G
ENST00000677685.1:c.*1898-50A>G	ENSP00000503407.1:n.*1898-50A>G
ENST00000677783.1:n.3143-50A>G
ENST00000677946.1:c.2673-50A>G	ENSP00000504202.1:n.2673-50A>G
ENST00000678024.1:n.2816-50A>G
ENST00000678647.1:n.806-50A>G
ENST00000678694.1:n.1994-50A>G
ENST00000678804.1:c.2673-50A>G	ENSP00000503853.1:n.2673-50A>G
ENST00000679100.1:n.860-50A>G
ENST00000679103.1:c.2673-50A>G	ENSP00000503151.1:n.2673-50A>G
ENST00000679313.1:c.2673-50A>G	ENSP00000504512.1:n.2673-50A>G
ENST00000340748.8:c.2673-50A>G	ENSP00000345739.3:n.2673-50A>G
ENST00000359526.8:c.2721-50A>G	ENSP00000352516.3:n.2721-50A>G
ENST00000540357.5:c.1665-50A>G	ENSP00000440457.2:n.1665-50A>G
ENST00000592705.5:c.*2411-50A>G	ENSP00000466657.1:n.*2411-50A>G
NM_001130823.1:c.2721-50A>G , LRG_362t1:c.2721-50A>G	NP_001124295.1:n.2721-50A>G
NM_001379.2:c.2673-50A>G	NP_001370.1:n.2673-50A>G
XM_011527772.1:c.2721-50A>G	XP_011526074.1:n.2721-50A>G
XM_011527773.1:c.2673-50A>G	XP_011526075.1:n.2673-50A>G
XM_011527774.1:c.2310-50A>G	XP_011526076.1:n.2310-50A>G
NM_001130823.2:c.2721-50A>G	NP_001124295.1:n.2721-50A>G
NM_001318730.1:c.2673-50A>G	NP_001305659.1:n.2673-50A>G
NM_001318731.1:c.2358-50A>G	NP_001305660.1:n.2358-50A>G
NM_001379.3:c.2673-50A>G	NP_001370.1:n.2673-50A>G
NM_001130823.3:c.2721-50A>G MANE Select	NP_001124295.1:n.2721-50A>G
NM_001318730.2:c.2673-50A>G	NP_001305659.1:n.2673-50A>G
NM_001318731.2:c.2358-50A>G	NP_001305660.1:n.2358-50A>G
NM_001379.4:c.2673-50A>G	NP_001370.1:n.2673-50A>G