Canonical Allele Identifier: CA2588330384
Gene: DNMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10156086C>A , CM000681.2:g.10156086C>A GRCh38
NC_000019.9:g.10266762C>A , CM000681.1:g.10266762C>A GRCh37
NC_000019.8:g.10127762C>A NCBI36
NG_028016.3:g.80201G>T , LRG_362:g.80201G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1400-141G>T MANE Select ENSP00000352516.3:n.1400-141G>T
ENST00000676604.1:n.1012-141G>T
ENST00000676610.1:c.1352-141G>T ENSP00000504236.1:n.1352-141G>T
ENST00000676820.1:n.1408-141G>T
ENST00000676868.1:n.2036-141G>T
ENST00000677013.1:c.*1042-141G>T ENSP00000503135.1:n.*1042-141G>T
ENST00000677250.1:c.*472-141G>T ENSP00000502894.1:n.*472-141G>T
ENST00000677616.1:c.1043-141G>T ENSP00000503055.1:n.1043-141G>T
ENST00000677634.1:c.1352-141G>T ENSP00000504246.1:n.1352-141G>T
ENST00000677685.1:c.*577-141G>T ENSP00000503407.1:n.*577-141G>T
ENST00000677783.1:n.1822-141G>T
ENST00000677946.1:c.1352-141G>T ENSP00000504202.1:n.1352-141G>T
ENST00000678024.1:n.1495-141G>T
ENST00000678694.1:n.673-141G>T
ENST00000678804.1:c.1352-141G>T ENSP00000503853.1:n.1352-141G>T
ENST00000679103.1:c.1352-141G>T ENSP00000503151.1:n.1352-141G>T
ENST00000679313.1:c.1352-141G>T ENSP00000504512.1:n.1352-141G>T
ENST00000340748.8:c.1352-141G>T ENSP00000345739.3:n.1352-141G>T
ENST00000359526.8:c.1400-141G>T ENSP00000352516.3:n.1400-141G>T
ENST00000540357.5:c.344-141G>T ENSP00000440457.2:n.344-141G>T
ENST00000585843.1:n.557-141G>T
ENST00000592705.5:c.*1090-141G>T ENSP00000466657.1:n.*1090-141G>T
NM_001130823.1:c.1400-141G>T , LRG_362t1:c.1400-141G>T NP_001124295.1:n.1400-141G>T
NM_001379.2:c.1352-141G>T NP_001370.1:n.1352-141G>T
XM_011527772.1:c.1400-141G>T XP_011526074.1:n.1400-141G>T
XM_011527773.1:c.1352-141G>T XP_011526075.1:n.1352-141G>T
XM_011527774.1:c.989-141G>T XP_011526076.1:n.989-141G>T
NM_001130823.2:c.1400-141G>T NP_001124295.1:n.1400-141G>T
NM_001318730.1:c.1352-141G>T NP_001305659.1:n.1352-141G>T
NM_001318731.1:c.1037-141G>T NP_001305660.1:n.1037-141G>T
NM_001379.3:c.1352-141G>T NP_001370.1:n.1352-141G>T
NM_001130823.3:c.1400-141G>T MANE Select NP_001124295.1:n.1400-141G>T
NM_001318730.2:c.1352-141G>T NP_001305659.1:n.1352-141G>T
NM_001318731.2:c.1037-141G>T NP_001305660.1:n.1037-141G>T
NM_001379.4:c.1352-141G>T NP_001370.1:n.1352-141G>T