Canonical Allele Identifier: CA403938133

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267114A>C (hg19) ; chr19:g.10156438A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156438A>C , CM000681.2:g.10156438A>C	GRCh38
NC_000019.9:g.10267114A>C , CM000681.1:g.10267114A>C	GRCh37
NC_000019.8:g.10128114A>C	NCBI36
NG_028016.3:g.79849T>G , LRG_362:g.79849T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1352T>G MANE Select	ENSP00000352516.3:p.Phe451Cys
ENST00000676604.1:n.964T>G
ENST00000676610.1:c.1304T>G	ENSP00000504236.1:p.Phe435Cys
ENST00000676820.1:n.1360T>G
ENST00000676868.1:n.1988T>G
ENST00000677013.1:c.*994T>G	ENSP00000503135.1:n.*994T>G
ENST00000677250.1:c.*424T>G	ENSP00000502894.1:n.*424T>G
ENST00000677616.1:c.995T>G	ENSP00000503055.1:p.Phe332Cys
ENST00000677634.1:c.1304T>G	ENSP00000504246.1:p.Phe435Cys
ENST00000677685.1:c.*529T>G	ENSP00000503407.1:n.*529T>G
ENST00000677783.1:n.1774T>G
ENST00000677946.1:c.1304T>G	ENSP00000504202.1:p.Phe435Cys
ENST00000678024.1:n.1447T>G
ENST00000678694.1:n.625T>G
ENST00000678804.1:c.1304T>G	ENSP00000503853.1:p.Phe435Cys
ENST00000679103.1:c.1304T>G	ENSP00000503151.1:p.Phe435Cys
ENST00000679313.1:c.1304T>G	ENSP00000504512.1:p.Phe435Cys
ENST00000340748.8:c.1304T>G	ENSP00000345739.3:p.Phe435Cys
ENST00000359526.8:c.1352T>G	ENSP00000352516.3:p.Phe451Cys
ENST00000540357.5:c.296T>G	ENSP00000440457.2:p.Phe99Cys
ENST00000585843.1:n.509T>G
ENST00000592705.5:c.*1042T>G	ENSP00000466657.1:n.*1042T>G
NM_001130823.1:c.1352T>G , LRG_362t1:c.1352T>G	NP_001124295.1:p.Phe451Cys
NM_001379.2:c.1304T>G	NP_001370.1:p.Phe435Cys
XM_011527772.1:c.1352T>G	XP_011526074.1:p.Phe451Cys
XM_011527773.1:c.1304T>G	XP_011526075.1:p.Phe435Cys
XM_011527774.1:c.941T>G	XP_011526076.1:p.Phe314Cys
NM_001130823.2:c.1352T>G	NP_001124295.1:p.Phe451Cys
NM_001318730.1:c.1304T>G	NP_001305659.1:p.Phe435Cys
NM_001318731.1:c.989T>G	NP_001305660.1:p.Phe330Cys
NM_001379.3:c.1304T>G	NP_001370.1:p.Phe435Cys
NM_001130823.3:c.1352T>G MANE Select	NP_001124295.1:p.Phe451Cys
NM_001318730.2:c.1304T>G	NP_001305659.1:p.Phe435Cys
NM_001318731.2:c.989T>G	NP_001305660.1:p.Phe330Cys
NM_001379.4:c.1304T>G	NP_001370.1:p.Phe435Cys