Canonical Allele Identifier: CA305172829

Gene: DNMT1

Linked Data

• dbSNP Id: rs1005174134
• gnomAD v2: 19-10266874-CTA-C
• gnomAD v3: 19-10156198-CTA-C
• gnomAD v4: 19-10156198-CTA-C
• MyVariant Identifiers: chr19:g.10266875_10266876del (hg19) ; chr19:g.10156199_10156200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10156208_10156209del , CM000681.2:g.10156208_10156209del	GRCh38
NC_000019.9:g.10266884_10266885del , CM000681.1:g.10266884_10266885del	GRCh37
NC_000019.8:g.10127884_10127885del	NCBI36
NG_028016.3:g.80087_80088del , LRG_362:g.80087_80088del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359526.9:c.1399+191_1399+192del MANE Select	ENSP00000352516.3:n.1399+191_1399+192del
ENST00000676604.1:n.1011+191_1011+192del
ENST00000676610.1:c.1351+191_1351+192del	ENSP00000504236.1:n.1351+191_1351+192del
ENST00000676820.1:n.1407+191_1407+192del
ENST00000676868.1:n.2035+191_2035+192del
ENST00000677013.1:c.*1041+191_*1041+192del	ENSP00000503135.1:n.*1041+191_*1041+192del
ENST00000677250.1:c.*471+191_*471+192del	ENSP00000502894.1:n.*471+191_*471+192del
ENST00000677616.1:c.1042+191_1042+192del	ENSP00000503055.1:n.1042+191_1042+192del
ENST00000677634.1:c.1351+191_1351+192del	ENSP00000504246.1:n.1351+191_1351+192del
ENST00000677685.1:c.*576+191_*576+192del	ENSP00000503407.1:n.*576+191_*576+192del
ENST00000677783.1:n.1821+191_1821+192del
ENST00000677946.1:c.1351+191_1351+192del	ENSP00000504202.1:n.1351+191_1351+192del
ENST00000678024.1:n.1494+191_1494+192del
ENST00000678694.1:n.672+191_672+192del
ENST00000678804.1:c.1351+191_1351+192del	ENSP00000503853.1:n.1351+191_1351+192del
ENST00000679103.1:c.1351+191_1351+192del	ENSP00000503151.1:n.1351+191_1351+192del
ENST00000679313.1:c.1351+191_1351+192del	ENSP00000504512.1:n.1351+191_1351+192del
ENST00000340748.8:c.1351+191_1351+192del	ENSP00000345739.3:n.1351+191_1351+192del
ENST00000359526.8:c.1399+191_1399+192del	ENSP00000352516.3:n.1399+191_1399+192del
ENST00000540357.5:c.343+191_343+192del	ENSP00000440457.2:n.343+191_343+192del
ENST00000585843.1:n.556+191_556+192del
ENST00000592705.5:c.*1089+191_*1089+192del	ENSP00000466657.1:n.*1089+191_*1089+192del
NM_001130823.1:c.1399+191_1399+192del , LRG_362t1:c.1399+191_1399+192del	NP_001124295.1:n.1399+191_1399+192del
NM_001379.2:c.1351+191_1351+192del	NP_001370.1:n.1351+191_1351+192del
XM_011527772.1:c.1399+191_1399+192del	XP_011526074.1:n.1399+191_1399+192del
XM_011527773.1:c.1351+191_1351+192del	XP_011526075.1:n.1351+191_1351+192del
XM_011527774.1:c.988+191_988+192del	XP_011526076.1:n.988+191_988+192del
NM_001130823.2:c.1399+191_1399+192del	NP_001124295.1:n.1399+191_1399+192del
NM_001318730.1:c.1351+191_1351+192del	NP_001305659.1:n.1351+191_1351+192del
NM_001318731.1:c.1036+191_1036+192del	NP_001305660.1:n.1036+191_1036+192del
NM_001379.3:c.1351+191_1351+192del	NP_001370.1:n.1351+191_1351+192del
NM_001130823.3:c.1399+191_1399+192del MANE Select	NP_001124295.1:n.1399+191_1399+192del
NM_001318730.2:c.1351+191_1351+192del	NP_001305659.1:n.1351+191_1351+192del
NM_001318731.2:c.1036+191_1036+192del	NP_001305660.1:n.1036+191_1036+192del
NM_001379.4:c.1351+191_1351+192del	NP_001370.1:n.1351+191_1351+192del