Canonical Allele Identifier: CA2658168082

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25234322-CGGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234323_25234325del , CM000664.2:g.25234323_25234325del	GRCh38
NC_000002.11:g.25457192_25457194del , CM000664.1:g.25457192_25457194del	GRCh37
NC_000002.10:g.25310696_25310698del	NCBI36
NG_029465.2:g.113266_113268del , LRG_459:g.113266_113268del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.942_944del
ENST00000683393.1:c.1839_1841del	ENSP00000508654.1:n.1839_1841del
ENST00000683760.1:c.2024_2026del	ENSP00000507765.1:p.Ile675_Arg676delinsSer
ENST00000321117.10:c.2693_2695del MANE Select	ENSP00000324375.5:p.Ile898_Arg899delinsSer
ENST00000264709.7:c.2693_2695del	ENSP00000264709.3:p.Ile898_Arg899delinsSer
ENST00000321117.9:c.2693_2695del	ENSP00000324375.5:p.Ile898_Arg899delinsSer
ENST00000380746.8:c.2126_2128del	ENSP00000370122.4:p.Ile709_Arg710delinsSer
ENST00000380756.7:c.*546_*548del	ENSP00000370132.3:n.*546_*548del
ENST00000402667.1:c.2024_2026del	ENSP00000384237.1:p.Ile675_Arg676delinsSer
NM_022552.4:c.2693_2695del , LRG_459t1:c.2693_2695del	NP_072046.2:p.Ile898_Arg899delinsSer
NM_153759.3:c.2126_2128del , LRG_459t2:c.2126_2128del	NP_715640.2:p.Ile709_Arg710delinsSer
NM_175629.2:c.2693_2695del , LRG_459t4:c.2693_2695del	NP_783328.1:p.Ile898_Arg899delinsSer
XM_005264175.3:c.2693_2695del	XP_005264232.1:p.Ile898_Arg899delinsSer
XM_005264177.3:c.2024_2026del	XP_005264234.1:p.Ile675_Arg676delinsSer
XM_006711958.2:c.2249_2251del	XP_006712021.1:p.Ile750_Arg751delinsSer
XM_011532662.1:c.2546_2548del	XP_011530964.1:p.Ile849_Arg850delinsSer
XM_011532663.1:c.2528_2530del	XP_011530965.1:p.Ile843_Arg844delinsSer
XM_011532665.1:c.2237_2239del	XP_011530967.1:p.Ile746_Arg747delinsSer
XM_011532666.1:c.2165_2167del	XP_011530968.1:p.Ile722_Arg723delinsSer
XM_011532667.1:c.2024_2026del	XP_011530969.1:p.Ile675_Arg676delinsSer
NM_001320893.1:c.2237_2239del	NP_001307822.1:p.Ile746_Arg747delinsSer
NR_135490.1:n.3230_3232del
XM_005264175.5:c.2693_2695del	XP_005264232.1:p.Ile898_Arg899delinsSer
XM_005264177.4:c.2024_2026del	XP_005264234.1:p.Ile675_Arg676delinsSer
XM_011532662.2:c.2546_2548del	XP_011530964.1:p.Ile849_Arg850delinsSer
XM_011532663.2:c.2528_2530del	XP_011530965.1:p.Ile843_Arg844delinsSer
XM_011532666.2:c.2165_2167del	XP_011530968.1:p.Ile722_Arg723delinsSer
XM_011532667.3:c.2024_2026del	XP_011530969.1:p.Ile675_Arg676delinsSer
XM_017003526.1:c.2693_2695del	XP_016859015.1:p.Ile898_Arg899delinsSer
XM_017003527.1:c.2024_2026del	XP_016859016.1:p.Ile675_Arg676delinsSer
XR_001738657.1:n.2900_2902del
NM_001375819.1:c.2024_2026del	NP_001362748.1:p.Ile675_Arg676delinsSer
NR_135490.2:n.3123_3125del
NM_022552.5:c.2693_2695del MANE Select	NP_072046.2:p.Ile898_Arg899delinsSer