Canonical Allele Identifier: CA505343541

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149930A>G , CM000681.2:g.10149930A>G	GRCh38
NC_000019.9:g.10260606A>G , CM000681.1:g.10260606A>G	GRCh37
NC_000019.8:g.10121606A>G	NCBI36
NG_028016.3:g.86357T>C , LRG_362:g.86357T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2304T>C MANE Select	ENSP00000352516.3:p.Ile768=
ENST00000586667.2:n.339T>C
ENST00000676604.1:n.1916T>C
ENST00000676610.1:c.2256T>C	ENSP00000504236.1:p.Ile752=
ENST00000676820.1:n.2312T>C
ENST00000676868.1:n.2940T>C
ENST00000677013.1:c.*1946T>C	ENSP00000503135.1:n.*1946T>C
ENST00000677250.1:c.*1376T>C	ENSP00000502894.1:n.*1376T>C
ENST00000677616.1:c.1947T>C	ENSP00000503055.1:p.Ile649=
ENST00000677634.1:c.2256T>C	ENSP00000504246.1:p.Ile752=
ENST00000677685.1:c.*1481T>C	ENSP00000503407.1:n.*1481T>C
ENST00000677783.1:n.2726T>C
ENST00000677946.1:c.2256T>C	ENSP00000504202.1:p.Ile752=
ENST00000678024.1:n.2399T>C
ENST00000678647.1:n.389T>C
ENST00000678694.1:n.1577T>C
ENST00000678804.1:c.2256T>C	ENSP00000503853.1:p.Ile752=
ENST00000679100.1:n.443T>C
ENST00000679103.1:c.2256T>C	ENSP00000503151.1:p.Ile752=
ENST00000679313.1:c.2256T>C	ENSP00000504512.1:p.Ile752=
ENST00000340748.8:c.2256T>C	ENSP00000345739.3:p.Ile752=
ENST00000359526.8:c.2304T>C	ENSP00000352516.3:p.Ile768=
ENST00000540357.5:c.1248T>C	ENSP00000440457.2:p.Ile416=
ENST00000586667.1:n.339T>C
ENST00000592705.5:c.*1994T>C	ENSP00000466657.1:n.*1994T>C
NM_001130823.1:c.2304T>C , LRG_362t1:c.2304T>C	NP_001124295.1:p.Ile768=
NM_001379.2:c.2256T>C	NP_001370.1:p.Ile752=
XM_011527772.1:c.2304T>C	XP_011526074.1:p.Ile768=
XM_011527773.1:c.2256T>C	XP_011526075.1:p.Ile752=
XM_011527774.1:c.1893T>C	XP_011526076.1:p.Ile631=
NM_001130823.2:c.2304T>C	NP_001124295.1:p.Ile768=
NM_001318730.1:c.2256T>C	NP_001305659.1:p.Ile752=
NM_001318731.1:c.1941T>C	NP_001305660.1:p.Ile647=
NM_001379.3:c.2256T>C	NP_001370.1:p.Ile752=
NM_001130823.3:c.2304T>C MANE Select	NP_001124295.1:p.Ile768=
NM_001318730.2:c.2256T>C	NP_001305659.1:p.Ile752=
NM_001318731.2:c.1941T>C	NP_001305660.1:p.Ile647=
NM_001379.4:c.2256T>C	NP_001370.1:p.Ile752=