Canonical Allele Identifier: CA783144646

Gene: DNMT1

Linked Data

• dbSNP Id: rs1218627391
• gnomAD v3: 19-10156092-GCACAAAGTCTCA-G
• gnomAD v4: 19-10156092-GCACAAAGTCTCA-G
• MyVariant Identifiers: chr19:g.10266769_10266780del (hg19) ; chr19:g.10156093_10156104del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156096_10156107del , CM000681.2:g.10156096_10156107del	GRCh38
NC_000019.9:g.10266772_10266783del , CM000681.1:g.10266772_10266783del	GRCh37
NC_000019.8:g.10127772_10127783del	NCBI36
NG_028016.3:g.80183_80194del , LRG_362:g.80183_80194del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1400-159_1400-148del MANE Select	ENSP00000352516.3:n.1400-159_1400-148del
ENST00000676604.1:n.1012-159_1012-148del
ENST00000676610.1:c.1352-159_1352-148del	ENSP00000504236.1:n.1352-159_1352-148del
ENST00000676820.1:n.1408-159_1408-148del
ENST00000676868.1:n.2036-159_2036-148del
ENST00000677013.1:c.*1042-159_*1042-148del	ENSP00000503135.1:n.*1042-159_*1042-148del
ENST00000677250.1:c.*472-159_*472-148del	ENSP00000502894.1:n.*472-159_*472-148del
ENST00000677616.1:c.1043-159_1043-148del	ENSP00000503055.1:n.1043-159_1043-148del
ENST00000677634.1:c.1352-159_1352-148del	ENSP00000504246.1:n.1352-159_1352-148del
ENST00000677685.1:c.*577-159_*577-148del	ENSP00000503407.1:n.*577-159_*577-148del
ENST00000677783.1:n.1822-159_1822-148del
ENST00000677946.1:c.1352-159_1352-148del	ENSP00000504202.1:n.1352-159_1352-148del
ENST00000678024.1:n.1495-159_1495-148del
ENST00000678694.1:n.673-159_673-148del
ENST00000678804.1:c.1352-159_1352-148del	ENSP00000503853.1:n.1352-159_1352-148del
ENST00000679103.1:c.1352-159_1352-148del	ENSP00000503151.1:n.1352-159_1352-148del
ENST00000679313.1:c.1352-159_1352-148del	ENSP00000504512.1:n.1352-159_1352-148del
ENST00000340748.8:c.1352-159_1352-148del	ENSP00000345739.3:n.1352-159_1352-148del
ENST00000359526.8:c.1400-159_1400-148del	ENSP00000352516.3:n.1400-159_1400-148del
ENST00000540357.5:c.344-159_344-148del	ENSP00000440457.2:n.344-159_344-148del
ENST00000585843.1:n.557-159_557-148del
ENST00000592705.5:c.*1090-159_*1090-148del	ENSP00000466657.1:n.*1090-159_*1090-148del
NM_001130823.1:c.1400-159_1400-148del , LRG_362t1:c.1400-159_1400-148del	NP_001124295.1:n.1400-159_1400-148del
NM_001379.2:c.1352-159_1352-148del	NP_001370.1:n.1352-159_1352-148del
XM_011527772.1:c.1400-159_1400-148del	XP_011526074.1:n.1400-159_1400-148del
XM_011527773.1:c.1352-159_1352-148del	XP_011526075.1:n.1352-159_1352-148del
XM_011527774.1:c.989-159_989-148del	XP_011526076.1:n.989-159_989-148del
NM_001130823.2:c.1400-159_1400-148del	NP_001124295.1:n.1400-159_1400-148del
NM_001318730.1:c.1352-159_1352-148del	NP_001305659.1:n.1352-159_1352-148del
NM_001318731.1:c.1037-159_1037-148del	NP_001305660.1:n.1037-159_1037-148del
NM_001379.3:c.1352-159_1352-148del	NP_001370.1:n.1352-159_1352-148del
NM_001130823.3:c.1400-159_1400-148del MANE Select	NP_001124295.1:n.1400-159_1400-148del
NM_001318730.2:c.1352-159_1352-148del	NP_001305659.1:n.1352-159_1352-148del
NM_001318731.2:c.1037-159_1037-148del	NP_001305660.1:n.1037-159_1037-148del
NM_001379.4:c.1352-159_1352-148del	NP_001370.1:n.1352-159_1352-148del