Canonical Allele Identifier: CA2658168066

Gene: DNMT3A

Linked Data

• gnomAD v4: 2-25234321-GCGGATGACTGGCACGCTCCATGAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234325_25234348del , CM000664.2:g.25234325_25234348del	GRCh38
NC_000002.11:g.25457194_25457217del , CM000664.1:g.25457194_25457217del	GRCh37
NC_000002.10:g.25310698_25310721del	NCBI36
NG_029465.2:g.113246_113269del , LRG_459:g.113246_113269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.922_945del
ENST00000683393.1:c.1819_1842del	ENSP00000508654.1:n.1819_1842del
ENST00000683760.1:c.2004_2027del	ENSP00000507765.1:p.Ser669_Arg676del
ENST00000321117.10:c.2673_2696del MANE Select	ENSP00000324375.5:p.Ser892_Arg899del
ENST00000264709.7:c.2673_2696del	ENSP00000264709.3:p.Ser892_Arg899del
ENST00000321117.9:c.2673_2696del	ENSP00000324375.5:p.Ser892_Arg899del
ENST00000380746.8:c.2106_2129del	ENSP00000370122.4:p.Ser703_Arg710del
ENST00000380756.7:c.*526_*549del	ENSP00000370132.3:n.*526_*549del
ENST00000402667.1:c.2004_2027del	ENSP00000384237.1:p.Ser669_Arg676del
NM_022552.4:c.2673_2696del , LRG_459t1:c.2673_2696del	NP_072046.2:p.Ser892_Arg899del
NM_153759.3:c.2106_2129del , LRG_459t2:c.2106_2129del	NP_715640.2:p.Ser703_Arg710del
NM_175629.2:c.2673_2696del , LRG_459t4:c.2673_2696del	NP_783328.1:p.Ser892_Arg899del
XM_005264175.3:c.2673_2696del	XP_005264232.1:p.Ser892_Arg899del
XM_005264177.3:c.2004_2027del	XP_005264234.1:p.Ser669_Arg676del
XM_006711958.2:c.2229_2252del	XP_006712021.1:p.Ser744_Arg751del
XM_011532662.1:c.2526_2549del	XP_011530964.1:p.Ser843_Arg850del
XM_011532663.1:c.2508_2531del	XP_011530965.1:p.Ser837_Arg844del
XM_011532665.1:c.2217_2240del	XP_011530967.1:p.Ser740_Arg747del
XM_011532666.1:c.2145_2168del	XP_011530968.1:p.Ser716_Arg723del
XM_011532667.1:c.2004_2027del	XP_011530969.1:p.Ser669_Arg676del
NM_001320893.1:c.2217_2240del	NP_001307822.1:p.Ser740_Arg747del
NR_135490.1:n.3210_3233del
XM_005264175.5:c.2673_2696del	XP_005264232.1:p.Ser892_Arg899del
XM_005264177.4:c.2004_2027del	XP_005264234.1:p.Ser669_Arg676del
XM_011532662.2:c.2526_2549del	XP_011530964.1:p.Ser843_Arg850del
XM_011532663.2:c.2508_2531del	XP_011530965.1:p.Ser837_Arg844del
XM_011532666.2:c.2145_2168del	XP_011530968.1:p.Ser716_Arg723del
XM_011532667.3:c.2004_2027del	XP_011530969.1:p.Ser669_Arg676del
XM_017003526.1:c.2673_2696del	XP_016859015.1:p.Ser892_Arg899del
XM_017003527.1:c.2004_2027del	XP_016859016.1:p.Ser669_Arg676del
XR_001738657.1:n.2880_2903del
NM_001375819.1:c.2004_2027del	NP_001362748.1:p.Ser669_Arg676del
NR_135490.2:n.3103_3126del
NM_022552.5:c.2673_2696del MANE Select	NP_072046.2:p.Ser892_Arg899del