Canonical Allele Identifier: CA403976351

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10257155T>A (hg19) ; chr19:g.10146479T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10146479T>A , CM000681.2:g.10146479T>A	GRCh38
NC_000019.9:g.10257155T>A , CM000681.1:g.10257155T>A	GRCh37
NC_000019.8:g.10118155T>A	NCBI36
NG_028016.3:g.89808A>T , LRG_362:g.89808A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359526.9:c.2766A>T MANE Select	ENSP00000352516.3:p.Glu922Asp
ENST00000586667.2:n.801A>T
ENST00000676604.1:n.2378A>T
ENST00000676610.1:c.2718A>T	ENSP00000504236.1:p.Glu906Asp
ENST00000676820.1:n.2774A>T
ENST00000676868.1:n.3402A>T
ENST00000677013.1:c.*2408A>T	ENSP00000503135.1:n.*2408A>T
ENST00000677250.1:c.*1838A>T	ENSP00000502894.1:n.*1838A>T
ENST00000677616.1:c.2409A>T	ENSP00000503055.1:p.Glu803Asp
ENST00000677634.1:c.2718A>T	ENSP00000504246.1:p.Glu906Asp
ENST00000677685.1:c.*1943A>T	ENSP00000503407.1:n.*1943A>T
ENST00000677783.1:n.3188A>T
ENST00000677946.1:c.2718A>T	ENSP00000504202.1:p.Glu906Asp
ENST00000678024.1:n.2861A>T
ENST00000678647.1:n.851A>T
ENST00000678694.1:n.2039A>T
ENST00000678804.1:c.2718A>T	ENSP00000503853.1:p.Glu906Asp
ENST00000679100.1:n.905A>T
ENST00000679103.1:c.2718A>T	ENSP00000503151.1:p.Glu906Asp
ENST00000679313.1:c.2718A>T	ENSP00000504512.1:p.Glu906Asp
ENST00000340748.8:c.2718A>T	ENSP00000345739.3:p.Glu906Asp
ENST00000359526.8:c.2766A>T	ENSP00000352516.3:p.Glu922Asp
ENST00000540357.5:c.1710A>T	ENSP00000440457.2:p.Glu570Asp
ENST00000592705.5:c.*2456A>T	ENSP00000466657.1:n.*2456A>T
NM_001130823.1:c.2766A>T , LRG_362t1:c.2766A>T	NP_001124295.1:p.Glu922Asp
NM_001379.2:c.2718A>T	NP_001370.1:p.Glu906Asp
XM_011527772.1:c.2766A>T	XP_011526074.1:p.Glu922Asp
XM_011527773.1:c.2718A>T	XP_011526075.1:p.Glu906Asp
XM_011527774.1:c.2355A>T	XP_011526076.1:p.Glu785Asp
NM_001130823.2:c.2766A>T	NP_001124295.1:p.Glu922Asp
NM_001318730.1:c.2718A>T	NP_001305659.1:p.Glu906Asp
NM_001318731.1:c.2403A>T	NP_001305660.1:p.Glu801Asp
NM_001379.3:c.2718A>T	NP_001370.1:p.Glu906Asp
NM_001130823.3:c.2766A>T MANE Select	NP_001124295.1:p.Glu922Asp
NM_001318730.2:c.2718A>T	NP_001305659.1:p.Glu906Asp
NM_001318731.2:c.2403A>T	NP_001305660.1:p.Glu801Asp
NM_001379.4:c.2718A>T	NP_001370.1:p.Glu906Asp