Canonical Allele Identifier: CA2322290332

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156444A= , CM000681.2:g.10156444A=	GRCh38
NC_000019.9:g.10267120A= , CM000681.1:g.10267120A=	GRCh37
NC_000019.8:g.10128120A=	NCBI36
NG_028016.3:g.79843T= , LRG_362:g.79843T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1346T= MANE Select	ENSP00000352516.3:p.Leu449=
ENST00000676604.1:n.958T=
ENST00000676610.1:c.1298T=	ENSP00000504236.1:p.Leu433=
ENST00000676820.1:n.1354T=
ENST00000676868.1:n.1982T=
ENST00000677013.1:c.*988T=	ENSP00000503135.1:n.*988T=
ENST00000677250.1:c.*418T=	ENSP00000502894.1:n.*418T=
ENST00000677616.1:c.989T=	ENSP00000503055.1:p.Leu330=
ENST00000677634.1:c.1298T=	ENSP00000504246.1:p.Leu433=
ENST00000677685.1:c.*523T=	ENSP00000503407.1:n.*523T=
ENST00000677783.1:n.1768T=
ENST00000677946.1:c.1298T=	ENSP00000504202.1:p.Leu433=
ENST00000678024.1:n.1441T=
ENST00000678694.1:n.619T=
ENST00000678804.1:c.1298T=	ENSP00000503853.1:p.Leu433=
ENST00000679103.1:c.1298T=	ENSP00000503151.1:p.Leu433=
ENST00000679313.1:c.1298T=	ENSP00000504512.1:p.Leu433=
ENST00000340748.8:c.1298T=	ENSP00000345739.3:p.Leu433=
ENST00000359526.8:c.1346T=	ENSP00000352516.3:p.Leu449=
ENST00000540357.5:c.290T=	ENSP00000440457.2:p.Leu97=
ENST00000585843.1:n.503T=
ENST00000592705.5:c.*1036T=	ENSP00000466657.1:n.*1036T=
NM_001130823.1:c.1346T= , LRG_362t1:c.1346T=	NP_001124295.1:p.Leu449=
NM_001379.2:c.1298T=	NP_001370.1:p.Leu433=
XM_011527772.1:c.1346T=	XP_011526074.1:p.Leu449=
XM_011527773.1:c.1298T=	XP_011526075.1:p.Leu433=
XM_011527774.1:c.935T=	XP_011526076.1:p.Leu312=
NM_001130823.2:c.1346T=	NP_001124295.1:p.Leu449=
NM_001318730.1:c.1298T=	NP_001305659.1:p.Leu433=
NM_001318731.1:c.983T=	NP_001305660.1:p.Leu328=
NM_001379.3:c.1298T=	NP_001370.1:p.Leu433=
NM_001130823.3:c.1346T= MANE Select	NP_001124295.1:p.Leu449=
NM_001318730.2:c.1298T=	NP_001305659.1:p.Leu433=
NM_001318731.2:c.983T=	NP_001305660.1:p.Leu328=
NM_001379.4:c.1298T=	NP_001370.1:p.Leu433=