Canonical Allele Identifier: CA2588329623

Gene: DNMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10149824_10149825insAAAA , CM000681.2:g.10149824_10149825insAAAA	GRCh38
NC_000019.9:g.10260500_10260501insAAAA , CM000681.1:g.10260500_10260501insAAAA	GRCh37
NC_000019.8:g.10121500_10121501insAAAA	NCBI36
NG_028016.3:g.86463_86464insTTTT , LRG_362:g.86463_86464insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.2381+29_2381+30insTTTT MANE Select	ENSP00000352516.3:n.2381+29_2381+30insTTTT
ENST00000586667.2:n.416+29_416+30insTTTT
ENST00000676604.1:n.1993+29_1993+30insTTTT
ENST00000676610.1:c.2333+29_2333+30insTTTT	ENSP00000504236.1:n.2333+29_2333+30insTTTT
ENST00000676820.1:n.2389+29_2389+30insTTTT
ENST00000676868.1:n.3017+29_3017+30insTTTT
ENST00000677013.1:c.*2023+29_*2023+30insTTTT	ENSP00000503135.1:n.*2023+29_*2023+30insTTTT
ENST00000677250.1:c.*1453+29_*1453+30insTTTT	ENSP00000502894.1:n.*1453+29_*1453+30insTTTT
ENST00000677616.1:c.2024+29_2024+30insTTTT	ENSP00000503055.1:n.2024+29_2024+30insTTTT
ENST00000677634.1:c.2333+29_2333+30insTTTT	ENSP00000504246.1:n.2333+29_2333+30insTTTT
ENST00000677685.1:c.*1558+29_*1558+30insTTTT	ENSP00000503407.1:n.*1558+29_*1558+30insTTTT
ENST00000677783.1:n.2803+29_2803+30insTTTT
ENST00000677946.1:c.2333+29_2333+30insTTTT	ENSP00000504202.1:n.2333+29_2333+30insTTTT
ENST00000678024.1:n.2476+29_2476+30insTTTT
ENST00000678647.1:n.466+29_466+30insTTTT
ENST00000678694.1:n.1654+29_1654+30insTTTT
ENST00000678804.1:c.2333+29_2333+30insTTTT	ENSP00000503853.1:n.2333+29_2333+30insTTTT
ENST00000679100.1:n.520+29_520+30insTTTT
ENST00000679103.1:c.2333+29_2333+30insTTTT	ENSP00000503151.1:n.2333+29_2333+30insTTTT
ENST00000679313.1:c.2333+29_2333+30insTTTT	ENSP00000504512.1:n.2333+29_2333+30insTTTT
ENST00000340748.8:c.2333+29_2333+30insTTTT	ENSP00000345739.3:n.2333+29_2333+30insTTTT
ENST00000359526.8:c.2381+29_2381+30insTTTT	ENSP00000352516.3:n.2381+29_2381+30insTTTT
ENST00000540357.5:c.1325+29_1325+30insTTTT	ENSP00000440457.2:n.1325+29_1325+30insTTTT
ENST00000586667.1:n.416+29_416+30insTTTT
ENST00000592705.5:c.*2071+29_*2071+30insTTTT	ENSP00000466657.1:n.*2071+29_*2071+30insTTTT
NM_001130823.1:c.2381+29_2381+30insTTTT , LRG_362t1:c.2381+29_2381+30insTTTT	NP_001124295.1:n.2381+29_2381+30insTTTT
NM_001379.2:c.2333+29_2333+30insTTTT	NP_001370.1:n.2333+29_2333+30insTTTT
XM_011527772.1:c.2381+29_2381+30insTTTT	XP_011526074.1:n.2381+29_2381+30insTTTT
XM_011527773.1:c.2333+29_2333+30insTTTT	XP_011526075.1:n.2333+29_2333+30insTTTT
XM_011527774.1:c.1970+29_1970+30insTTTT	XP_011526076.1:n.1970+29_1970+30insTTTT
NM_001130823.2:c.2381+29_2381+30insTTTT	NP_001124295.1:n.2381+29_2381+30insTTTT
NM_001318730.1:c.2333+29_2333+30insTTTT	NP_001305659.1:n.2333+29_2333+30insTTTT
NM_001318731.1:c.2018+29_2018+30insTTTT	NP_001305660.1:n.2018+29_2018+30insTTTT
NM_001379.3:c.2333+29_2333+30insTTTT	NP_001370.1:n.2333+29_2333+30insTTTT
NM_001130823.3:c.2381+29_2381+30insTTTT MANE Select	NP_001124295.1:n.2381+29_2381+30insTTTT
NM_001318730.2:c.2333+29_2333+30insTTTT	NP_001305659.1:n.2333+29_2333+30insTTTT
NM_001318731.2:c.2018+29_2018+30insTTTT	NP_001305660.1:n.2018+29_2018+30insTTTT
NM_001379.4:c.2333+29_2333+30insTTTT	NP_001370.1:n.2333+29_2333+30insTTTT