Canonical Allele Identifier: CA631709533

Gene: DNMT1

Linked Data

• dbSNP Id: rs1480497062
• gnomAD v2: 19-10265193-A-AGAG
• gnomAD v3: 19-10154517-A-AGAG
• gnomAD v4: 19-10154517-A-AGAG
• MyVariant Identifiers: chr19:g.10265193_10265194insGAG (hg19) ; chr19:g.10154517_10154518insGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10154520_10154522dup , CM000681.2:g.10154520_10154522dup	GRCh38
NC_000019.9:g.10265196_10265198dup , CM000681.1:g.10265196_10265198dup	GRCh37
NC_000019.8:g.10126196_10126198dup	NCBI36
NG_028016.3:g.81767_81769dup , LRG_362:g.81767_81769dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1833-41_1833-39dup MANE Select	ENSP00000352516.3:n.1833-41_1833-39dup
ENST00000676604.1:n.1445-41_1445-39dup
ENST00000676610.1:c.1785-41_1785-39dup	ENSP00000504236.1:n.1785-41_1785-39dup
ENST00000676820.1:n.1841-41_1841-39dup
ENST00000676868.1:n.2469-41_2469-39dup
ENST00000677013.1:c.*1475-41_*1475-39dup	ENSP00000503135.1:n.*1475-41_*1475-39dup
ENST00000677250.1:c.*905-41_*905-39dup	ENSP00000502894.1:n.*905-41_*905-39dup
ENST00000677616.1:c.1476-41_1476-39dup	ENSP00000503055.1:n.1476-41_1476-39dup
ENST00000677634.1:c.1785-41_1785-39dup	ENSP00000504246.1:n.1785-41_1785-39dup
ENST00000677685.1:c.*1010-41_*1010-39dup	ENSP00000503407.1:n.*1010-41_*1010-39dup
ENST00000677783.1:n.2255-41_2255-39dup
ENST00000677946.1:c.1785-41_1785-39dup	ENSP00000504202.1:n.1785-41_1785-39dup
ENST00000678024.1:n.1928-41_1928-39dup
ENST00000678694.1:n.1106-41_1106-39dup
ENST00000678804.1:c.1785-41_1785-39dup	ENSP00000503853.1:n.1785-41_1785-39dup
ENST00000679103.1:c.1785-41_1785-39dup	ENSP00000503151.1:n.1785-41_1785-39dup
ENST00000679313.1:c.1785-41_1785-39dup	ENSP00000504512.1:n.1785-41_1785-39dup
ENST00000340748.8:c.1785-41_1785-39dup	ENSP00000345739.3:n.1785-41_1785-39dup
ENST00000359526.8:c.1833-41_1833-39dup	ENSP00000352516.3:n.1833-41_1833-39dup
ENST00000540357.5:c.777-41_777-39dup	ENSP00000440457.2:n.777-41_777-39dup
ENST00000586799.1:c.219-41_219-39dup
ENST00000592705.5:c.*1523-41_*1523-39dup	ENSP00000466657.1:n.*1523-41_*1523-39dup
NM_001130823.1:c.1833-41_1833-39dup , LRG_362t1:c.1833-41_1833-39dup	NP_001124295.1:n.1833-41_1833-39dup
NM_001379.2:c.1785-41_1785-39dup	NP_001370.1:n.1785-41_1785-39dup
XM_011527772.1:c.1833-41_1833-39dup	XP_011526074.1:n.1833-41_1833-39dup
XM_011527773.1:c.1785-41_1785-39dup	XP_011526075.1:n.1785-41_1785-39dup
XM_011527774.1:c.1422-41_1422-39dup	XP_011526076.1:n.1422-41_1422-39dup
NM_001130823.2:c.1833-41_1833-39dup	NP_001124295.1:n.1833-41_1833-39dup
NM_001318730.1:c.1785-41_1785-39dup	NP_001305659.1:n.1785-41_1785-39dup
NM_001318731.1:c.1470-41_1470-39dup	NP_001305660.1:n.1470-41_1470-39dup
NM_001379.3:c.1785-41_1785-39dup	NP_001370.1:n.1785-41_1785-39dup
NM_001130823.3:c.1833-41_1833-39dup MANE Select	NP_001124295.1:n.1833-41_1833-39dup
NM_001318730.2:c.1785-41_1785-39dup	NP_001305659.1:n.1785-41_1785-39dup
NM_001318731.2:c.1470-41_1470-39dup	NP_001305660.1:n.1470-41_1470-39dup
NM_001379.4:c.1785-41_1785-39dup	NP_001370.1:n.1785-41_1785-39dup