Canonical Allele Identifier: CA505346855
Gene: DNMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.10267155G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10156479G>C , CM000681.2:g.10156479G>C GRCh38
NC_000019.9:g.10267155G>C , CM000681.1:g.10267155G>C GRCh37
NC_000019.8:g.10128155G>C NCBI36
NG_028016.3:g.79808C>G , LRG_362:g.79808C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000359526.9:c.1311C>G MANE Select ENSP00000352516.3:p.Pro437=
ENST00000676604.1:n.923C>G
ENST00000676610.1:c.1263C>G ENSP00000504236.1:p.Pro421=
ENST00000676820.1:n.1319C>G
ENST00000676868.1:n.1947C>G
ENST00000677013.1:c.*953C>G ENSP00000503135.1:n.*953C>G
ENST00000677250.1:c.*383C>G ENSP00000502894.1:n.*383C>G
ENST00000677616.1:c.954C>G ENSP00000503055.1:p.Pro318=
ENST00000677634.1:c.1263C>G ENSP00000504246.1:p.Pro421=
ENST00000677685.1:c.*488C>G ENSP00000503407.1:n.*488C>G
ENST00000677783.1:n.1733C>G
ENST00000677946.1:c.1263C>G ENSP00000504202.1:p.Pro421=
ENST00000678024.1:n.1406C>G
ENST00000678694.1:n.584C>G
ENST00000678804.1:c.1263C>G ENSP00000503853.1:p.Pro421=
ENST00000679103.1:c.1263C>G ENSP00000503151.1:p.Pro421=
ENST00000679313.1:c.1263C>G ENSP00000504512.1:p.Pro421=
ENST00000340748.8:c.1263C>G ENSP00000345739.3:p.Pro421=
ENST00000359526.8:c.1311C>G ENSP00000352516.3:p.Pro437=
ENST00000540357.5:c.255C>G ENSP00000440457.2:p.Pro85=
ENST00000585843.1:n.468C>G
ENST00000592705.5:c.*1001C>G ENSP00000466657.1:n.*1001C>G
NM_001130823.1:c.1311C>G , LRG_362t1:c.1311C>G NP_001124295.1:p.Pro437=
NM_001379.2:c.1263C>G NP_001370.1:p.Pro421=
XM_011527772.1:c.1311C>G XP_011526074.1:p.Pro437=
XM_011527773.1:c.1263C>G XP_011526075.1:p.Pro421=
XM_011527774.1:c.900C>G XP_011526076.1:p.Pro300=
NM_001130823.2:c.1311C>G NP_001124295.1:p.Pro437=
NM_001318730.1:c.1263C>G NP_001305659.1:p.Pro421=
NM_001318731.1:c.948C>G NP_001305660.1:p.Pro316=
NM_001379.3:c.1263C>G NP_001370.1:p.Pro421=
NM_001130823.3:c.1311C>G MANE Select NP_001124295.1:p.Pro437=
NM_001318730.2:c.1263C>G NP_001305659.1:p.Pro421=
NM_001318731.2:c.948C>G NP_001305660.1:p.Pro316=
NM_001379.4:c.1263C>G NP_001370.1:p.Pro421=