Canonical Allele Identifier: CA1028506307

Gene: DNMT3A

Linked Data

• gnomAD v3: 2-25240353-AT-A
• gnomAD v4: 2-25240353-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25240355del , CM000664.2:g.25240355del	GRCh38
NC_000002.11:g.25463224del , CM000664.1:g.25463224del	GRCh37
NC_000002.10:g.25316728del	NCBI36
NG_029465.2:g.107237del , LRG_459:g.107237del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.589del
ENST00000683393.1:c.1416del	ENSP00000508654.1:n.1416del
ENST00000683760.1:c.1601del	ENSP00000507765.1:p.Asn534MetfsTer22
ENST00000321117.10:c.2270del MANE Select	ENSP00000324375.5:p.Asn757MetfsTer22
ENST00000264709.7:c.2270del	ENSP00000264709.3:p.Asn757MetfsTer22
ENST00000321117.9:c.2270del	ENSP00000324375.5:p.Asn757MetfsTer22
ENST00000380746.8:c.1703del	ENSP00000370122.4:p.Asn568MetfsTer22
ENST00000380756.7:c.2270del	ENSP00000370132.3:p.Asn757MetfsTer?
ENST00000402667.1:c.1601del	ENSP00000384237.1:p.Asn534MetfsTer22
ENST00000461228.1:n.489del
ENST00000466601.5:n.642del
ENST00000474887.5:n.589del
ENST00000482935.5:n.270del
ENST00000491288.5:n.310+286del
NM_022552.4:c.2270del , LRG_459t1:c.2270del	NP_072046.2:p.Asn757MetfsTer22
NM_153759.3:c.1703del , LRG_459t2:c.1703del	NP_715640.2:p.Asn568MetfsTer22
NM_175629.2:c.2270del , LRG_459t4:c.2270del	NP_783328.1:p.Asn757MetfsTer22
XM_005264175.3:c.2270del	XP_005264232.1:p.Asn757MetfsTer22
XM_005264177.3:c.1601del	XP_005264234.1:p.Asn534MetfsTer22
XM_006711957.2:c.2270del	XP_006712020.1:p.Asn757MetfsTer22
XM_006711958.2:c.1826del	XP_006712021.1:p.Asn609MetfsTer22
XM_011532662.1:c.2123del	XP_011530964.1:p.Asn708MetfsTer22
XM_011532663.1:c.2105del	XP_011530965.1:p.Asn702MetfsTer22
XM_011532664.1:c.2270del	XP_011530966.1:p.Asn757MetfsTer?
XM_011532665.1:c.1814del	XP_011530967.1:p.Asn605MetfsTer22
XM_011532666.1:c.1742del	XP_011530968.1:p.Asn581MetfsTer22
XM_011532667.1:c.1601del	XP_011530969.1:p.Asn534MetfsTer22
XM_011532668.1:c.2270del	XP_011530970.1:p.Asn757MetfsTer?
NM_001320893.1:c.1814del	NP_001307822.1:p.Asn605MetfsTer22
NR_135490.1:n.2608del
XM_005264175.5:c.2270del	XP_005264232.1:p.Asn757MetfsTer22
XM_005264177.4:c.1601del	XP_005264234.1:p.Asn534MetfsTer22
XM_011532662.2:c.2123del	XP_011530964.1:p.Asn708MetfsTer22
XM_011532663.2:c.2105del	XP_011530965.1:p.Asn702MetfsTer22
XM_011532664.2:c.2270del	XP_011530966.1:p.Asn757MetfsTer?
XM_011532666.2:c.1742del	XP_011530968.1:p.Asn581MetfsTer22
XM_011532667.3:c.1601del	XP_011530969.1:p.Asn534MetfsTer22
XM_017003526.1:c.2270del	XP_016859015.1:p.Asn757MetfsTer22
XM_017003527.1:c.1601del	XP_016859016.1:p.Asn534MetfsTer22
XR_001738657.1:n.2547del
NM_001375819.1:c.1601del	NP_001362748.1:p.Asn534MetfsTer22
NR_135490.2:n.2501del
NM_022552.5:c.2270del MANE Select	NP_072046.2:p.Asn757MetfsTer22