Canonical Allele Identifier: CA2322290342

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156493C= , CM000681.2:g.10156493C=	GRCh38
NC_000019.9:g.10267169C= , CM000681.1:g.10267169C=	GRCh37
NC_000019.8:g.10128169C=	NCBI36
NG_028016.3:g.79794G= , LRG_362:g.79794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1297G= MANE Select	ENSP00000352516.3:p.Gly433=
ENST00000676604.1:n.909G=
ENST00000676610.1:c.1249G=	ENSP00000504236.1:p.Gly417=
ENST00000676820.1:n.1305G=
ENST00000676868.1:n.1933G=
ENST00000677013.1:c.*939G=	ENSP00000503135.1:n.*939G=
ENST00000677250.1:c.*369G=	ENSP00000502894.1:n.*369G=
ENST00000677616.1:c.940G=	ENSP00000503055.1:p.Gly314=
ENST00000677634.1:c.1249G=	ENSP00000504246.1:p.Gly417=
ENST00000677685.1:c.*474G=	ENSP00000503407.1:n.*474G=
ENST00000677783.1:n.1719G=
ENST00000677946.1:c.1249G=	ENSP00000504202.1:p.Gly417=
ENST00000678024.1:n.1392G=
ENST00000678694.1:n.570G=
ENST00000678804.1:c.1249G=	ENSP00000503853.1:p.Gly417=
ENST00000679103.1:c.1249G=	ENSP00000503151.1:p.Gly417=
ENST00000679313.1:c.1249G=	ENSP00000504512.1:p.Gly417=
ENST00000340748.8:c.1249G=	ENSP00000345739.3:p.Gly417=
ENST00000359526.8:c.1297G=	ENSP00000352516.3:p.Gly433=
ENST00000540357.5:c.241G=	ENSP00000440457.2:p.Gly81=
ENST00000585843.1:n.454G=
ENST00000592705.5:c.*987G=	ENSP00000466657.1:n.*987G=
NM_001130823.1:c.1297G= , LRG_362t1:c.1297G=	NP_001124295.1:p.Gly433=
NM_001379.2:c.1249G=	NP_001370.1:p.Gly417=
XM_011527772.1:c.1297G=	XP_011526074.1:p.Gly433=
XM_011527773.1:c.1249G=	XP_011526075.1:p.Gly417=
XM_011527774.1:c.886G=	XP_011526076.1:p.Gly296=
NM_001130823.2:c.1297G=	NP_001124295.1:p.Gly433=
NM_001318730.1:c.1249G=	NP_001305659.1:p.Gly417=
NM_001318731.1:c.934G=	NP_001305660.1:p.Gly312=
NM_001379.3:c.1249G=	NP_001370.1:p.Gly417=
NM_001130823.3:c.1297G= MANE Select	NP_001124295.1:p.Gly433=
NM_001318730.2:c.1249G=	NP_001305659.1:p.Gly417=
NM_001318731.2:c.934G=	NP_001305660.1:p.Gly312=
NM_001379.4:c.1249G=	NP_001370.1:p.Gly417=