Canonical Allele Identifier: CA403938040

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267091A>C (hg19) ; chr19:g.10156415A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156415A>C , CM000681.2:g.10156415A>C	GRCh38
NC_000019.9:g.10267091A>C , CM000681.1:g.10267091A>C	GRCh37
NC_000019.8:g.10128091A>C	NCBI36
NG_028016.3:g.79872T>G , LRG_362:g.79872T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1375T>G MANE Select	ENSP00000352516.3:p.Tyr459Asp
ENST00000676604.1:n.987T>G
ENST00000676610.1:c.1327T>G	ENSP00000504236.1:p.Tyr443Asp
ENST00000676820.1:n.1383T>G
ENST00000676868.1:n.2011T>G
ENST00000677013.1:c.*1017T>G	ENSP00000503135.1:n.*1017T>G
ENST00000677250.1:c.*447T>G	ENSP00000502894.1:n.*447T>G
ENST00000677616.1:c.1018T>G	ENSP00000503055.1:p.Tyr340Asp
ENST00000677634.1:c.1327T>G	ENSP00000504246.1:p.Tyr443Asp
ENST00000677685.1:c.*552T>G	ENSP00000503407.1:n.*552T>G
ENST00000677783.1:n.1797T>G
ENST00000677946.1:c.1327T>G	ENSP00000504202.1:p.Tyr443Asp
ENST00000678024.1:n.1470T>G
ENST00000678694.1:n.648T>G
ENST00000678804.1:c.1327T>G	ENSP00000503853.1:p.Tyr443Asp
ENST00000679103.1:c.1327T>G	ENSP00000503151.1:p.Tyr443Asp
ENST00000679313.1:c.1327T>G	ENSP00000504512.1:p.Tyr443Asp
ENST00000340748.8:c.1327T>G	ENSP00000345739.3:p.Tyr443Asp
ENST00000359526.8:c.1375T>G	ENSP00000352516.3:p.Tyr459Asp
ENST00000540357.5:c.319T>G	ENSP00000440457.2:p.Tyr107Asp
ENST00000585843.1:n.532T>G
ENST00000592705.5:c.*1065T>G	ENSP00000466657.1:n.*1065T>G
NM_001130823.1:c.1375T>G , LRG_362t1:c.1375T>G	NP_001124295.1:p.Tyr459Asp
NM_001379.2:c.1327T>G	NP_001370.1:p.Tyr443Asp
XM_011527772.1:c.1375T>G	XP_011526074.1:p.Tyr459Asp
XM_011527773.1:c.1327T>G	XP_011526075.1:p.Tyr443Asp
XM_011527774.1:c.964T>G	XP_011526076.1:p.Tyr322Asp
NM_001130823.2:c.1375T>G	NP_001124295.1:p.Tyr459Asp
NM_001318730.1:c.1327T>G	NP_001305659.1:p.Tyr443Asp
NM_001318731.1:c.1012T>G	NP_001305660.1:p.Tyr338Asp
NM_001379.3:c.1327T>G	NP_001370.1:p.Tyr443Asp
NM_001130823.3:c.1375T>G MANE Select	NP_001124295.1:p.Tyr459Asp
NM_001318730.2:c.1327T>G	NP_001305659.1:p.Tyr443Asp
NM_001318731.2:c.1012T>G	NP_001305660.1:p.Tyr338Asp
NM_001379.4:c.1327T>G	NP_001370.1:p.Tyr443Asp