Canonical Allele Identifier: CA403950190
Gene: DNMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10194845A>T , CM000681.2:g.10194845A>T GRCh38
NC_000019.9:g.10305521A>T , CM000681.1:g.10305521A>T GRCh37
NC_000019.8:g.10166521A>T NCBI36
NG_028016.3:g.41442T>A , LRG_362:g.41442T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.55T>A MANE Select ENSP00000352516.3:p.Ser19Thr
ENST00000676610.1:c.55T>A ENSP00000504236.1:p.Ser19Thr
ENST00000676820.1:n.111T>A
ENST00000677013.1:c.55T>A ENSP00000503135.1:p.Ser19Thr
ENST00000677250.1:c.55T>A ENSP00000502894.1:p.Ser19Thr
ENST00000677634.1:c.55T>A ENSP00000504246.1:p.Ser19Thr
ENST00000677685.1:c.55T>A ENSP00000503407.1:p.Ser19Thr
ENST00000677946.1:c.55T>A ENSP00000504202.1:p.Ser19Thr
ENST00000678804.1:c.55T>A ENSP00000503853.1:p.Ser19Thr
ENST00000679103.1:c.55T>A ENSP00000503151.1:p.Ser19Thr
ENST00000679313.1:c.55T>A ENSP00000504512.1:p.Ser19Thr
ENST00000340748.8:c.55T>A ENSP00000345739.3:p.Ser19Thr
ENST00000359526.8:c.55T>A ENSP00000352516.3:p.Ser19Thr
ENST00000540357.5:c.-561+98T>A ENSP00000440457.2:n.-561+98T>A
ENST00000586800.5:c.-284+6029T>A ENSP00000465555.1:n.-284+6029T>A
ENST00000586988.5:c.55T>A ENSP00000464958.1:p.Ser19Thr
ENST00000588118.5:c.220T>A ENSP00000465223.1:p.Ser74Thr
ENST00000588952.5:c.-283-12768T>A ENSP00000467050.1:n.-283-12768T>A
ENST00000592342.5:c.-283-12768T>A ENSP00000465993.1:n.-283-12768T>A
ENST00000592705.5:c.55T>A ENSP00000466657.1:p.Ser19Thr
NM_001130823.1:c.55T>A , LRG_362t1:c.55T>A NP_001124295.1:p.Ser19Thr
NM_001379.2:c.55T>A NP_001370.1:p.Ser19Thr
XM_011527772.1:c.55T>A XP_011526074.1:p.Ser19Thr
XM_011527773.1:c.55T>A XP_011526075.1:p.Ser19Thr
NM_001130823.2:c.55T>A NP_001124295.1:p.Ser19Thr
NM_001318730.1:c.55T>A NP_001305659.1:p.Ser19Thr
NM_001318731.1:c.-269T>A NP_001305660.1:n.-269T>A
NM_001379.3:c.55T>A NP_001370.1:p.Ser19Thr
NM_001130823.3:c.55T>A MANE Select NP_001124295.1:p.Ser19Thr
NM_001318730.2:c.55T>A NP_001305659.1:p.Ser19Thr
NM_001318731.2:c.-269T>A NP_001305660.1:n.-269T>A
NM_001379.4:c.55T>A NP_001370.1:p.Ser19Thr