Canonical Allele Identifier: CA2588333530

Gene: DNMT1

Linked Data

• gnomAD v4: 19-10180321-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10180321T>G , CM000681.2:g.10180321T>G	GRCh38
NC_000019.9:g.10290997T>G , CM000681.1:g.10290997T>G	GRCh37
NC_000019.8:g.10151997T>G	NCBI36
NG_028016.3:g.55966A>C , LRG_362:g.55966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.445+29A>C MANE Select	ENSP00000352516.3:n.445+29A>C
ENST00000676610.1:c.445+29A>C	ENSP00000504236.1:n.445+29A>C
ENST00000676820.1:n.501+29A>C
ENST00000677013.1:c.*135+29A>C	ENSP00000503135.1:n.*135+29A>C
ENST00000677250.1:c.445+29A>C	ENSP00000502894.1:n.445+29A>C
ENST00000677616.1:c.82+29A>C	ENSP00000503055.1:n.82+29A>C
ENST00000677634.1:c.445+29A>C	ENSP00000504246.1:n.445+29A>C
ENST00000677685.1:c.225+457A>C	ENSP00000503407.1:n.225+457A>C
ENST00000677946.1:c.445+29A>C	ENSP00000504202.1:n.445+29A>C
ENST00000678804.1:c.445+29A>C	ENSP00000503853.1:n.445+29A>C
ENST00000679103.1:c.445+29A>C	ENSP00000503151.1:n.445+29A>C
ENST00000679313.1:c.445+29A>C	ENSP00000504512.1:n.445+29A>C
ENST00000340748.8:c.445+29A>C	ENSP00000345739.3:n.445+29A>C
ENST00000359526.8:c.445+29A>C	ENSP00000352516.3:n.445+29A>C
ENST00000540357.5:c.-560-2957A>C	ENSP00000440457.2:n.-560-2957A>C
ENST00000586988.5:c.*273+29A>C	ENSP00000464958.1:n.*273+29A>C
ENST00000588118.5:c.610+29A>C	ENSP00000465223.1:n.610+29A>C
ENST00000588952.5:c.82+29A>C	ENSP00000467050.1:n.82+29A>C
ENST00000590619.1:c.32+29A>C
ENST00000592054.5:c.82+29A>C	ENSP00000468359.1:n.82+29A>C
ENST00000592342.5:c.82+29A>C	ENSP00000465993.1:n.82+29A>C
ENST00000592705.5:c.*135+29A>C	ENSP00000466657.1:n.*135+29A>C
NM_001130823.1:c.445+29A>C , LRG_362t1:c.445+29A>C	NP_001124295.1:n.445+29A>C
NM_001379.2:c.445+29A>C	NP_001370.1:n.445+29A>C
XM_011527772.1:c.445+29A>C	XP_011526074.1:n.445+29A>C
XM_011527773.1:c.445+29A>C	XP_011526075.1:n.445+29A>C
XM_011527774.1:c.82+29A>C	XP_011526076.1:n.82+29A>C
NM_001130823.2:c.445+29A>C	NP_001124295.1:n.445+29A>C
NM_001318730.1:c.445+29A>C	NP_001305659.1:n.445+29A>C
NM_001318731.1:c.82+29A>C	NP_001305660.1:n.82+29A>C
NM_001379.3:c.445+29A>C	NP_001370.1:n.445+29A>C
NM_001130823.3:c.445+29A>C MANE Select	NP_001124295.1:n.445+29A>C
NM_001318730.2:c.445+29A>C	NP_001305659.1:n.445+29A>C
NM_001318731.2:c.82+29A>C	NP_001305660.1:n.82+29A>C
NM_001379.4:c.445+29A>C	NP_001370.1:n.445+29A>C