Canonical Allele Identifier: CA403976347

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257153A>G (hg19) ; chr19:g.10146477A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146477A>G , CM000681.2:g.10146477A>G	GRCh38
NC_000019.9:g.10257153A>G , CM000681.1:g.10257153A>G	GRCh37
NC_000019.8:g.10118153A>G	NCBI36
NG_028016.3:g.89810T>C , LRG_362:g.89810T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2768T>C MANE Select	ENSP00000352516.3:p.Ile923Thr
ENST00000586667.2:n.803T>C
ENST00000676604.1:n.2380T>C
ENST00000676610.1:c.2720T>C	ENSP00000504236.1:p.Ile907Thr
ENST00000676820.1:n.2776T>C
ENST00000676868.1:n.3404T>C
ENST00000677013.1:c.*2410T>C	ENSP00000503135.1:n.*2410T>C
ENST00000677250.1:c.*1840T>C	ENSP00000502894.1:n.*1840T>C
ENST00000677616.1:c.2411T>C	ENSP00000503055.1:p.Ile804Thr
ENST00000677634.1:c.2720T>C	ENSP00000504246.1:p.Ile907Thr
ENST00000677685.1:c.*1945T>C	ENSP00000503407.1:n.*1945T>C
ENST00000677783.1:n.3190T>C
ENST00000677946.1:c.2720T>C	ENSP00000504202.1:p.Ile907Thr
ENST00000678024.1:n.2863T>C
ENST00000678647.1:n.853T>C
ENST00000678694.1:n.2041T>C
ENST00000678804.1:c.2720T>C	ENSP00000503853.1:p.Ile907Thr
ENST00000679100.1:n.907T>C
ENST00000679103.1:c.2720T>C	ENSP00000503151.1:p.Ile907Thr
ENST00000679313.1:c.2720T>C	ENSP00000504512.1:p.Ile907Thr
ENST00000340748.8:c.2720T>C	ENSP00000345739.3:p.Ile907Thr
ENST00000359526.8:c.2768T>C	ENSP00000352516.3:p.Ile923Thr
ENST00000540357.5:c.1712T>C	ENSP00000440457.2:p.Ile571Thr
ENST00000592705.5:c.*2458T>C	ENSP00000466657.1:n.*2458T>C
NM_001130823.1:c.2768T>C , LRG_362t1:c.2768T>C	NP_001124295.1:p.Ile923Thr
NM_001379.2:c.2720T>C	NP_001370.1:p.Ile907Thr
XM_011527772.1:c.2768T>C	XP_011526074.1:p.Ile923Thr
XM_011527773.1:c.2720T>C	XP_011526075.1:p.Ile907Thr
XM_011527774.1:c.2357T>C	XP_011526076.1:p.Ile786Thr
NM_001130823.2:c.2768T>C	NP_001124295.1:p.Ile923Thr
NM_001318730.1:c.2720T>C	NP_001305659.1:p.Ile907Thr
NM_001318731.1:c.2405T>C	NP_001305660.1:p.Ile802Thr
NM_001379.3:c.2720T>C	NP_001370.1:p.Ile907Thr
NM_001130823.3:c.2768T>C MANE Select	NP_001124295.1:p.Ile923Thr
NM_001318730.2:c.2720T>C	NP_001305659.1:p.Ile907Thr
NM_001318731.2:c.2405T>C	NP_001305660.1:p.Ile802Thr
NM_001379.4:c.2720T>C	NP_001370.1:p.Ile907Thr