Canonical Allele Identifier: CA305172816

Gene: DNMT1

Linked Data

• dbSNP Id: rs549847345
• gnomAD v2: 19-10266827-CATAAGT-C
• gnomAD v3: 19-10156151-CATAAGT-C
• gnomAD v4: 19-10156151-CATAAGT-C
• MyVariant Identifiers: chr19:g.10266828_10266833del (hg19) ; chr19:g.10156152_10156157del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156154_10156159del , CM000681.2:g.10156154_10156159del	GRCh38
NC_000019.9:g.10266830_10266835del , CM000681.1:g.10266830_10266835del	GRCh37
NC_000019.8:g.10127830_10127835del	NCBI36
NG_028016.3:g.80130_80135del , LRG_362:g.80130_80135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-212_1400-207del MANE Select	ENSP00000352516.3:n.1400-212_1400-207del
ENST00000676604.1:n.1012-212_1012-207del
ENST00000676610.1:c.1352-212_1352-207del	ENSP00000504236.1:n.1352-212_1352-207del
ENST00000676820.1:n.1408-212_1408-207del
ENST00000676868.1:n.2036-212_2036-207del
ENST00000677013.1:c.*1042-212_*1042-207del	ENSP00000503135.1:n.*1042-212_*1042-207del
ENST00000677250.1:c.*472-212_*472-207del	ENSP00000502894.1:n.*472-212_*472-207del
ENST00000677616.1:c.1043-212_1043-207del	ENSP00000503055.1:n.1043-212_1043-207del
ENST00000677634.1:c.1352-212_1352-207del	ENSP00000504246.1:n.1352-212_1352-207del
ENST00000677685.1:c.*577-212_*577-207del	ENSP00000503407.1:n.*577-212_*577-207del
ENST00000677783.1:n.1822-212_1822-207del
ENST00000677946.1:c.1352-212_1352-207del	ENSP00000504202.1:n.1352-212_1352-207del
ENST00000678024.1:n.1495-212_1495-207del
ENST00000678694.1:n.673-212_673-207del
ENST00000678804.1:c.1352-212_1352-207del	ENSP00000503853.1:n.1352-212_1352-207del
ENST00000679103.1:c.1352-212_1352-207del	ENSP00000503151.1:n.1352-212_1352-207del
ENST00000679313.1:c.1352-212_1352-207del	ENSP00000504512.1:n.1352-212_1352-207del
ENST00000340748.8:c.1352-212_1352-207del	ENSP00000345739.3:n.1352-212_1352-207del
ENST00000359526.8:c.1400-212_1400-207del	ENSP00000352516.3:n.1400-212_1400-207del
ENST00000540357.5:c.344-212_344-207del	ENSP00000440457.2:n.344-212_344-207del
ENST00000585843.1:n.557-212_557-207del
ENST00000592705.5:c.*1090-212_*1090-207del	ENSP00000466657.1:n.*1090-212_*1090-207del
NM_001130823.1:c.1400-212_1400-207del , LRG_362t1:c.1400-212_1400-207del	NP_001124295.1:n.1400-212_1400-207del
NM_001379.2:c.1352-212_1352-207del	NP_001370.1:n.1352-212_1352-207del
XM_011527772.1:c.1400-212_1400-207del	XP_011526074.1:n.1400-212_1400-207del
XM_011527773.1:c.1352-212_1352-207del	XP_011526075.1:n.1352-212_1352-207del
XM_011527774.1:c.989-212_989-207del	XP_011526076.1:n.989-212_989-207del
NM_001130823.2:c.1400-212_1400-207del	NP_001124295.1:n.1400-212_1400-207del
NM_001318730.1:c.1352-212_1352-207del	NP_001305659.1:n.1352-212_1352-207del
NM_001318731.1:c.1037-212_1037-207del	NP_001305660.1:n.1037-212_1037-207del
NM_001379.3:c.1352-212_1352-207del	NP_001370.1:n.1352-212_1352-207del
NM_001130823.3:c.1400-212_1400-207del MANE Select	NP_001124295.1:n.1400-212_1400-207del
NM_001318730.2:c.1352-212_1352-207del	NP_001305659.1:n.1352-212_1352-207del
NM_001318731.2:c.1037-212_1037-207del	NP_001305660.1:n.1037-212_1037-207del
NM_001379.4:c.1352-212_1352-207del	NP_001370.1:n.1352-212_1352-207del