Canonical Allele Identifier: CA505346758

Gene: DNMT1

Linked Data

• dbSNP Id: rs1288860393
• gnomAD v3: 19-10156413-A-G
• gnomAD v4: 19-10156413-A-G
• MyVariant Identifiers: chr19:g.10267089A>G (hg19) ; chr19:g.10156413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156413A>G , CM000681.2:g.10156413A>G	GRCh38
NC_000019.9:g.10267089A>G , CM000681.1:g.10267089A>G	GRCh37
NC_000019.8:g.10128089A>G	NCBI36
NG_028016.3:g.79874T>C , LRG_362:g.79874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1377T>C MANE Select	ENSP00000352516.3:p.Tyr459=
ENST00000676604.1:n.989T>C
ENST00000676610.1:c.1329T>C	ENSP00000504236.1:p.Tyr443=
ENST00000676820.1:n.1385T>C
ENST00000676868.1:n.2013T>C
ENST00000677013.1:c.*1019T>C	ENSP00000503135.1:n.*1019T>C
ENST00000677250.1:c.*449T>C	ENSP00000502894.1:n.*449T>C
ENST00000677616.1:c.1020T>C	ENSP00000503055.1:p.Tyr340=
ENST00000677634.1:c.1329T>C	ENSP00000504246.1:p.Tyr443=
ENST00000677685.1:c.*554T>C	ENSP00000503407.1:n.*554T>C
ENST00000677783.1:n.1799T>C
ENST00000677946.1:c.1329T>C	ENSP00000504202.1:p.Tyr443=
ENST00000678024.1:n.1472T>C
ENST00000678694.1:n.650T>C
ENST00000678804.1:c.1329T>C	ENSP00000503853.1:p.Tyr443=
ENST00000679103.1:c.1329T>C	ENSP00000503151.1:p.Tyr443=
ENST00000679313.1:c.1329T>C	ENSP00000504512.1:p.Tyr443=
ENST00000340748.8:c.1329T>C	ENSP00000345739.3:p.Tyr443=
ENST00000359526.8:c.1377T>C	ENSP00000352516.3:p.Tyr459=
ENST00000540357.5:c.321T>C	ENSP00000440457.2:p.Tyr107=
ENST00000585843.1:n.534T>C
ENST00000592705.5:c.*1067T>C	ENSP00000466657.1:n.*1067T>C
NM_001130823.1:c.1377T>C , LRG_362t1:c.1377T>C	NP_001124295.1:p.Tyr459=
NM_001379.2:c.1329T>C	NP_001370.1:p.Tyr443=
XM_011527772.1:c.1377T>C	XP_011526074.1:p.Tyr459=
XM_011527773.1:c.1329T>C	XP_011526075.1:p.Tyr443=
XM_011527774.1:c.966T>C	XP_011526076.1:p.Tyr322=
NM_001130823.2:c.1377T>C	NP_001124295.1:p.Tyr459=
NM_001318730.1:c.1329T>C	NP_001305659.1:p.Tyr443=
NM_001318731.1:c.1014T>C	NP_001305660.1:p.Tyr338=
NM_001379.3:c.1329T>C	NP_001370.1:p.Tyr443=
NM_001130823.3:c.1377T>C MANE Select	NP_001124295.1:p.Tyr459=
NM_001318730.2:c.1329T>C	NP_001305659.1:p.Tyr443=
NM_001318731.2:c.1014T>C	NP_001305660.1:p.Tyr338=
NM_001379.4:c.1329T>C	NP_001370.1:p.Tyr443=