Canonical Allele Identifier: CA2658168474

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25244206-G-GTCCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25244209_25244213dup , CM000664.2:g.25244209_25244213dup	GRCh38
NC_000002.11:g.25467078_25467082dup , CM000664.1:g.25467078_25467082dup	GRCh37
NC_000002.10:g.25320582_25320586dup	NCBI36
NG_029465.2:g.103380_103384dup , LRG_459:g.103380_103384dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.114_118dup
ENST00000683393.1:c.941_945dup	ENSP00000508654.1:n.941_945dup
ENST00000683760.1:c.1126_1130dup	ENSP00000507765.1:p.Asp377GlufsTer?
ENST00000321117.10:c.1795_1799dup MANE Select	ENSP00000324375.5:p.Asp600GlufsTer?
ENST00000264709.7:c.1795_1799dup	ENSP00000264709.3:p.Asp600GlufsTer?
ENST00000321117.9:c.1795_1799dup	ENSP00000324375.5:p.Asp600GlufsTer?
ENST00000380746.8:c.1228_1232dup	ENSP00000370122.4:p.Asp411GlufsTer?
ENST00000380756.7:c.1795_1799dup	ENSP00000370132.3:p.Asp600GlufsTer?
ENST00000402667.1:c.1126_1130dup	ENSP00000384237.1:p.Asp377GlufsTer?
ENST00000474887.5:n.114_118dup
NM_022552.4:c.1795_1799dup , LRG_459t1:c.1795_1799dup	NP_072046.2:p.Asp600GlufsTer?
NM_153759.3:c.1228_1232dup , LRG_459t2:c.1228_1232dup	NP_715640.2:p.Asp411GlufsTer?
NM_175629.2:c.1795_1799dup , LRG_459t4:c.1795_1799dup	NP_783328.1:p.Asp600GlufsTer?
XM_005264175.3:c.1795_1799dup	XP_005264232.1:p.Asp600GlufsTer?
XM_005264177.3:c.1126_1130dup	XP_005264234.1:p.Asp377GlufsTer?
XM_006711957.2:c.1795_1799dup	XP_006712020.1:p.Asp600GlufsTer?
XM_006711958.2:c.1351_1355dup	XP_006712021.1:p.Asp452GlufsTer?
XM_011532662.1:c.1648_1652dup	XP_011530964.1:p.Asp551GlufsTer?
XM_011532663.1:c.1630_1634dup	XP_011530965.1:p.Asp545GlufsTer?
XM_011532664.1:c.1795_1799dup	XP_011530966.1:p.Asp600GlufsTer?
XM_011532665.1:c.1339_1343dup	XP_011530967.1:p.Asp448GlufsTer?
XM_011532666.1:c.1267_1271dup	XP_011530968.1:p.Asp424GlufsTer?
XM_011532667.1:c.1126_1130dup	XP_011530969.1:p.Asp377GlufsTer?
XM_011532668.1:c.1795_1799dup	XP_011530970.1:p.Asp600GlufsTer?
NM_001320893.1:c.1339_1343dup	NP_001307822.1:p.Asp448GlufsTer?
NR_135490.1:n.2133_2137dup
XM_005264175.5:c.1795_1799dup	XP_005264232.1:p.Asp600GlufsTer?
XM_005264177.4:c.1126_1130dup	XP_005264234.1:p.Asp377GlufsTer?
XM_011532662.2:c.1648_1652dup	XP_011530964.1:p.Asp551GlufsTer?
XM_011532663.2:c.1630_1634dup	XP_011530965.1:p.Asp545GlufsTer?
XM_011532664.2:c.1795_1799dup	XP_011530966.1:p.Asp600GlufsTer?
XM_011532666.2:c.1267_1271dup	XP_011530968.1:p.Asp424GlufsTer?
XM_011532667.3:c.1126_1130dup	XP_011530969.1:p.Asp377GlufsTer?
XM_017003526.1:c.1795_1799dup	XP_016859015.1:p.Asp600GlufsTer?
XM_017003527.1:c.1126_1130dup	XP_016859016.1:p.Asp377GlufsTer?
XR_001738657.1:n.2072_2076dup
NM_001375819.1:c.1126_1130dup	NP_001362748.1:p.Asp377GlufsTer?
NR_135490.2:n.2026_2030dup
NM_022552.5:c.1795_1799dup MANE Select	NP_072046.2:p.Asp600GlufsTer?