Canonical Allele Identifier: CA505346730

Gene: DNMT1

Linked Data

• MyVariant Identifiers: chr19:g.10267071A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156395A>G , CM000681.2:g.10156395A>G	GRCh38
NC_000019.9:g.10267071A>G , CM000681.1:g.10267071A>G	GRCh37
NC_000019.8:g.10128071A>G	NCBI36
NG_028016.3:g.79892T>C , LRG_362:g.79892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1395T>C MANE Select	ENSP00000352516.3:p.Leu465=
ENST00000676604.1:n.1007T>C
ENST00000676610.1:c.1347T>C	ENSP00000504236.1:p.Leu449=
ENST00000676820.1:n.1403T>C
ENST00000676868.1:n.2031T>C
ENST00000677013.1:c.*1037T>C	ENSP00000503135.1:n.*1037T>C
ENST00000677250.1:c.*467T>C	ENSP00000502894.1:n.*467T>C
ENST00000677616.1:c.1038T>C	ENSP00000503055.1:p.Leu346=
ENST00000677634.1:c.1347T>C	ENSP00000504246.1:p.Leu449=
ENST00000677685.1:c.*572T>C	ENSP00000503407.1:n.*572T>C
ENST00000677783.1:n.1817T>C
ENST00000677946.1:c.1347T>C	ENSP00000504202.1:p.Leu449=
ENST00000678024.1:n.1490T>C
ENST00000678694.1:n.668T>C
ENST00000678804.1:c.1347T>C	ENSP00000503853.1:p.Leu449=
ENST00000679103.1:c.1347T>C	ENSP00000503151.1:p.Leu449=
ENST00000679313.1:c.1347T>C	ENSP00000504512.1:p.Leu449=
ENST00000340748.8:c.1347T>C	ENSP00000345739.3:p.Leu449=
ENST00000359526.8:c.1395T>C	ENSP00000352516.3:p.Leu465=
ENST00000540357.5:c.339T>C	ENSP00000440457.2:p.Leu113=
ENST00000585843.1:n.552T>C
ENST00000592705.5:c.*1085T>C	ENSP00000466657.1:n.*1085T>C
NM_001130823.1:c.1395T>C , LRG_362t1:c.1395T>C	NP_001124295.1:p.Leu465=
NM_001379.2:c.1347T>C	NP_001370.1:p.Leu449=
XM_011527772.1:c.1395T>C	XP_011526074.1:p.Leu465=
XM_011527773.1:c.1347T>C	XP_011526075.1:p.Leu449=
XM_011527774.1:c.984T>C	XP_011526076.1:p.Leu328=
NM_001130823.2:c.1395T>C	NP_001124295.1:p.Leu465=
NM_001318730.1:c.1347T>C	NP_001305659.1:p.Leu449=
NM_001318731.1:c.1032T>C	NP_001305660.1:p.Leu344=
NM_001379.3:c.1347T>C	NP_001370.1:p.Leu449=
NM_001130823.3:c.1395T>C MANE Select	NP_001124295.1:p.Leu465=
NM_001318730.2:c.1347T>C	NP_001305659.1:p.Leu449=
NM_001318731.2:c.1032T>C	NP_001305660.1:p.Leu344=
NM_001379.4:c.1347T>C	NP_001370.1:p.Leu449=