Canonical Allele Identifier: CA2322306653

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10189741A= , CM000681.2:g.10189741A=	GRCh38
NC_000019.9:g.10300417A= , CM000681.1:g.10300417A=	GRCh37
NC_000019.8:g.10161417A=	NCBI36
NG_028016.3:g.46546T= , LRG_362:g.46546T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001130823.3:c.80+5079T= MANE Select	NP_001124295.1:n.80+5079T=
ENST00000359526.9:c.80+5079T= MANE Select	ENSP00000352516.3:n.80+5079T=
NM_001130823.1:c.80+5079T= , LRG_362t1:c.80+5079T=	NP_001124295.1:n.80+5079T=
NM_001130823.2:c.80+5079T=	NP_001124295.1:n.80+5079T=
NM_001318730.1:c.80+5079T=	NP_001305659.1:n.80+5079T=
NM_001318730.2:c.80+5079T=	NP_001305659.1:n.80+5079T=
NM_001318731.1:c.-244+5079T=	NP_001305660.1:n.-244+5079T=
NM_001318731.2:c.-244+5079T=	NP_001305660.1:n.-244+5079T=
NM_001379.2:c.80+5079T=	NP_001370.1:n.80+5079T=
NM_001379.3:c.80+5079T=	NP_001370.1:n.80+5079T=
NM_001379.4:c.80+5079T=	NP_001370.1:n.80+5079T=
ENST00000340748.8:c.80+5079T=	ENSP00000345739.3:n.80+5079T=
ENST00000359526.8:c.80+5079T=	ENSP00000352516.3:n.80+5079T=
ENST00000540357.5:c.-561+5202T=	ENSP00000440457.2:n.-561+5202T=
ENST00000586800.5:c.-283-7664T=	ENSP00000465555.1:n.-283-7664T=
ENST00000586988.5:c.80+5079T=	ENSP00000464958.1:n.80+5079T=
ENST00000588118.5:c.245+5079T=	ENSP00000465223.1:n.245+5079T=
ENST00000588952.5:c.-283-7664T=	ENSP00000467050.1:n.-283-7664T=
ENST00000592054.5:c.-284+4792T=	ENSP00000468359.1:n.-284+4792T=
ENST00000592342.5:c.-283-7664T=	ENSP00000465993.1:n.-283-7664T=
ENST00000592705.5:c.80+5079T=	ENSP00000466657.1:n.80+5079T=
ENST00000676610.1:c.80+5079T=	ENSP00000504236.1:n.80+5079T=
ENST00000676820.1:n.136+5079T=
ENST00000677013.1:c.80+5079T=	ENSP00000503135.1:n.80+5079T=
ENST00000677250.1:c.80+5079T=	ENSP00000502894.1:n.80+5079T=
ENST00000677634.1:c.80+5079T=	ENSP00000504246.1:n.80+5079T=
ENST00000677685.1:c.80+5079T=	ENSP00000503407.1:n.80+5079T=
ENST00000677946.1:c.80+5079T=	ENSP00000504202.1:n.80+5079T=
ENST00000678804.1:c.80+5079T=	ENSP00000503853.1:n.80+5079T=
ENST00000679103.1:c.80+5079T=	ENSP00000503151.1:n.80+5079T=
ENST00000679313.1:c.80+5079T=	ENSP00000504512.1:n.80+5079T=
XM_011527772.1:c.80+5079T=	XP_011526074.1:n.80+5079T=
XM_011527773.1:c.80+5079T=	XP_011526075.1:n.80+5079T=
XM_011527774.1:c.-284+4792T=	XP_011526076.1:n.-284+4792T=