Canonical Allele Identifier: CA2658168149

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25234332-GCACGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234333_25234337del , CM000664.2:g.25234333_25234337del	GRCh38
NC_000002.11:g.25457202_25457206del , CM000664.1:g.25457202_25457206del	GRCh37
NC_000002.10:g.25310706_25310710del	NCBI36
NG_029465.2:g.113254_113258del , LRG_459:g.113254_113258del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.930_934del
ENST00000683393.1:c.1827_1831del	ENSP00000508654.1:n.1827_1831del
ENST00000683760.1:c.2012_2016del	ENSP00000507765.1:p.Ser671ThrfsTer25
ENST00000321117.10:c.2681_2685del MANE Select	ENSP00000324375.5:p.Ser894ThrfsTer25
ENST00000264709.7:c.2681_2685del	ENSP00000264709.3:p.Ser894ThrfsTer25
ENST00000321117.9:c.2681_2685del	ENSP00000324375.5:p.Ser894ThrfsTer25
ENST00000380746.8:c.2114_2118del	ENSP00000370122.4:p.Ser705ThrfsTer25
ENST00000380756.7:c.*534_*538del	ENSP00000370132.3:n.*534_*538del
ENST00000402667.1:c.2012_2016del	ENSP00000384237.1:p.Ser671ThrfsTer25
NM_022552.4:c.2681_2685del , LRG_459t1:c.2681_2685del	NP_072046.2:p.Ser894ThrfsTer25
NM_153759.3:c.2114_2118del , LRG_459t2:c.2114_2118del	NP_715640.2:p.Ser705ThrfsTer25
NM_175629.2:c.2681_2685del , LRG_459t4:c.2681_2685del	NP_783328.1:p.Ser894ThrfsTer25
XM_005264175.3:c.2681_2685del	XP_005264232.1:p.Ser894ThrfsTer25
XM_005264177.3:c.2012_2016del	XP_005264234.1:p.Ser671ThrfsTer25
XM_006711958.2:c.2237_2241del	XP_006712021.1:p.Ser746ThrfsTer25
XM_011532662.1:c.2534_2538del	XP_011530964.1:p.Ser845ThrfsTer25
XM_011532663.1:c.2516_2520del	XP_011530965.1:p.Ser839ThrfsTer25
XM_011532665.1:c.2225_2229del	XP_011530967.1:p.Ser742ThrfsTer25
XM_011532666.1:c.2153_2157del	XP_011530968.1:p.Ser718ThrfsTer25
XM_011532667.1:c.2012_2016del	XP_011530969.1:p.Ser671ThrfsTer25
NM_001320893.1:c.2225_2229del	NP_001307822.1:p.Ser742ThrfsTer25
NR_135490.1:n.3218_3222del
XM_005264175.5:c.2681_2685del	XP_005264232.1:p.Ser894ThrfsTer25
XM_005264177.4:c.2012_2016del	XP_005264234.1:p.Ser671ThrfsTer25
XM_011532662.2:c.2534_2538del	XP_011530964.1:p.Ser845ThrfsTer25
XM_011532663.2:c.2516_2520del	XP_011530965.1:p.Ser839ThrfsTer25
XM_011532666.2:c.2153_2157del	XP_011530968.1:p.Ser718ThrfsTer25
XM_011532667.3:c.2012_2016del	XP_011530969.1:p.Ser671ThrfsTer25
XM_017003526.1:c.2681_2685del	XP_016859015.1:p.Ser894ThrfsTer25
XM_017003527.1:c.2012_2016del	XP_016859016.1:p.Ser671ThrfsTer25
XR_001738657.1:n.2888_2892del
NM_001375819.1:c.2012_2016del	NP_001362748.1:p.Ser671ThrfsTer25
NR_135490.2:n.3111_3115del
NM_022552.5:c.2681_2685del MANE Select	NP_072046.2:p.Ser894ThrfsTer25