Canonical Allele Identifier: CA2322285574
Gene: DNMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10146369G= , CM000681.2:g.10146369G= GRCh38
NC_000019.9:g.10257045G= , CM000681.1:g.10257045G= GRCh37
NC_000019.8:g.10118045G= NCBI36
NG_028016.3:g.89918C= , LRG_362:g.89918C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.2876C= MANE Select ENSP00000352516.3:p.Pro959=
ENST00000586667.2:n.911C=
ENST00000676604.1:n.2488C=
ENST00000676610.1:c.2828C= ENSP00000504236.1:p.Pro943=
ENST00000676820.1:n.2884C=
ENST00000676868.1:n.3512C=
ENST00000677013.1:c.*2518C= ENSP00000503135.1:n.*2518C=
ENST00000677250.1:c.*1948C= ENSP00000502894.1:n.*1948C=
ENST00000677616.1:c.2519C= ENSP00000503055.1:p.Pro840=
ENST00000677634.1:c.2828C= ENSP00000504246.1:p.Pro943=
ENST00000677685.1:c.*2053C= ENSP00000503407.1:n.*2053C=
ENST00000677783.1:n.3298C=
ENST00000677946.1:c.2828C= ENSP00000504202.1:p.Pro943=
ENST00000678024.1:n.2971C=
ENST00000678647.1:n.961C=
ENST00000678694.1:n.2149C=
ENST00000678804.1:c.2828C= ENSP00000503853.1:p.Pro943=
ENST00000679100.1:n.1015C=
ENST00000679103.1:c.2828C= ENSP00000503151.1:p.Pro943=
ENST00000679313.1:c.2828C= ENSP00000504512.1:p.Pro943=
ENST00000340748.8:c.2828C= ENSP00000345739.3:p.Pro943=
ENST00000359526.8:c.2876C= ENSP00000352516.3:p.Pro959=
ENST00000540357.5:c.1820C= ENSP00000440457.2:p.Pro607=
ENST00000592705.5:c.*2566C= ENSP00000466657.1:n.*2566C=
NM_001130823.1:c.2876C= , LRG_362t1:c.2876C= NP_001124295.1:p.Pro959=
NM_001379.2:c.2828C= NP_001370.1:p.Pro943=
XM_011527772.1:c.2876C= XP_011526074.1:p.Pro959=
XM_011527773.1:c.2828C= XP_011526075.1:p.Pro943=
XM_011527774.1:c.2465C= XP_011526076.1:p.Pro822=
NM_001130823.2:c.2876C= NP_001124295.1:p.Pro959=
NM_001318730.1:c.2828C= NP_001305659.1:p.Pro943=
NM_001318731.1:c.2513C= NP_001305660.1:p.Pro838=
NM_001379.3:c.2828C= NP_001370.1:p.Pro943=
NM_001130823.3:c.2876C= MANE Select NP_001124295.1:p.Pro959=
NM_001318730.2:c.2828C= NP_001305659.1:p.Pro943=
NM_001318731.2:c.2513C= NP_001305660.1:p.Pro838=
NM_001379.4:c.2828C= NP_001370.1:p.Pro943=