Canonical Allele Identifier: CA2576694289

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244217-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244219del , CM000664.2:g.25244219del	GRCh38
NC_000002.11:g.25467088del , CM000664.1:g.25467088del	GRCh37
NC_000002.10:g.25320592del	NCBI36
NG_029465.2:g.103373del , LRG_459:g.103373del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.107del
ENST00000683393.1:c.934del	ENSP00000508654.1:n.934del
ENST00000683760.1:c.1119del	ENSP00000507765.1:p.Arg374GlyfsTer?
ENST00000321117.10:c.1788del MANE Select	ENSP00000324375.5:p.Arg597GlyfsTer?
ENST00000264709.7:c.1788del	ENSP00000264709.3:p.Arg597GlyfsTer?
ENST00000321117.9:c.1788del	ENSP00000324375.5:p.Arg597GlyfsTer?
ENST00000380746.8:c.1221del	ENSP00000370122.4:p.Arg408GlyfsTer?
ENST00000380756.7:c.1788del	ENSP00000370132.3:p.Arg597GlyfsTer?
ENST00000402667.1:c.1119del	ENSP00000384237.1:p.Arg374GlyfsTer?
ENST00000474887.5:n.107del
NM_022552.4:c.1788del , LRG_459t1:c.1788del	NP_072046.2:p.Arg597GlyfsTer?
NM_153759.3:c.1221del , LRG_459t2:c.1221del	NP_715640.2:p.Arg408GlyfsTer?
NM_175629.2:c.1788del , LRG_459t4:c.1788del	NP_783328.1:p.Arg597GlyfsTer?
XM_005264175.3:c.1788del	XP_005264232.1:p.Arg597GlyfsTer?
XM_005264177.3:c.1119del	XP_005264234.1:p.Arg374GlyfsTer?
XM_006711957.2:c.1788del	XP_006712020.1:p.Arg597GlyfsTer?
XM_006711958.2:c.1344del	XP_006712021.1:p.Arg449GlyfsTer?
XM_011532662.1:c.1641del	XP_011530964.1:p.Arg548GlyfsTer?
XM_011532663.1:c.1623del	XP_011530965.1:p.Arg542GlyfsTer?
XM_011532664.1:c.1788del	XP_011530966.1:p.Arg597GlyfsTer?
XM_011532665.1:c.1332del	XP_011530967.1:p.Arg445GlyfsTer?
XM_011532666.1:c.1260del	XP_011530968.1:p.Arg421GlyfsTer?
XM_011532667.1:c.1119del	XP_011530969.1:p.Arg374GlyfsTer?
XM_011532668.1:c.1788del	XP_011530970.1:p.Arg597GlyfsTer?
NM_001320893.1:c.1332del	NP_001307822.1:p.Arg445GlyfsTer?
NR_135490.1:n.2126del
XM_005264175.5:c.1788del	XP_005264232.1:p.Arg597GlyfsTer?
XM_005264177.4:c.1119del	XP_005264234.1:p.Arg374GlyfsTer?
XM_011532662.2:c.1641del	XP_011530964.1:p.Arg548GlyfsTer?
XM_011532663.2:c.1623del	XP_011530965.1:p.Arg542GlyfsTer?
XM_011532664.2:c.1788del	XP_011530966.1:p.Arg597GlyfsTer?
XM_011532666.2:c.1260del	XP_011530968.1:p.Arg421GlyfsTer?
XM_011532667.3:c.1119del	XP_011530969.1:p.Arg374GlyfsTer?
XM_017003526.1:c.1788del	XP_016859015.1:p.Arg597GlyfsTer?
XM_017003527.1:c.1119del	XP_016859016.1:p.Arg374GlyfsTer?
XR_001738657.1:n.2065del
NM_001375819.1:c.1119del	NP_001362748.1:p.Arg374GlyfsTer?
NR_135490.2:n.2019del
NM_022552.5:c.1788del MANE Select	NP_072046.2:p.Arg597GlyfsTer?