Canonical Allele Identifier: CA1028525344

Gene: DNMT3A

Linked Data

• gnomAD v3: 2-25234315-GAGGTGGCGGATGACTGGCACGCTCCAT-G
• gnomAD v4: 2-25234315-GAGGTGGCGGATGACTGGCACGCTCCAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234316_25234342del , CM000664.2:g.25234316_25234342del	GRCh38
NC_000002.11:g.25457185_25457211del , CM000664.1:g.25457185_25457211del	GRCh37
NC_000002.10:g.25310689_25310715del	NCBI36
NG_029465.2:g.113249_113275del , LRG_459:g.113249_113275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.925_951del
ENST00000683393.1:c.1822_1848del	ENSP00000508654.1:n.1822_1848del
ENST00000683760.1:c.2007_2033del	ENSP00000507765.1:p.Trp670_Leu678del
ENST00000321117.10:c.2676_2702del MANE Select	ENSP00000324375.5:p.Trp893_Leu901del
ENST00000264709.7:c.2676_2702del	ENSP00000264709.3:p.Trp893_Leu901del
ENST00000321117.9:c.2676_2702del	ENSP00000324375.5:p.Trp893_Leu901del
ENST00000380746.8:c.2109_2135del	ENSP00000370122.4:p.Trp704_Leu712del
ENST00000380756.7:c.*529_*555del	ENSP00000370132.3:n.*529_*555del
ENST00000402667.1:c.2007_2033del	ENSP00000384237.1:p.Trp670_Leu678del
NM_022552.4:c.2676_2702del , LRG_459t1:c.2676_2702del	NP_072046.2:p.Trp893_Leu901del
NM_153759.3:c.2109_2135del , LRG_459t2:c.2109_2135del	NP_715640.2:p.Trp704_Leu712del
NM_175629.2:c.2676_2702del , LRG_459t4:c.2676_2702del	NP_783328.1:p.Trp893_Leu901del
XM_005264175.3:c.2676_2702del	XP_005264232.1:p.Trp893_Leu901del
XM_005264177.3:c.2007_2033del	XP_005264234.1:p.Trp670_Leu678del
XM_006711958.2:c.2232_2258del	XP_006712021.1:p.Trp745_Leu753del
XM_011532662.1:c.2529_2555del	XP_011530964.1:p.Trp844_Leu852del
XM_011532663.1:c.2511_2537del	XP_011530965.1:p.Trp838_Leu846del
XM_011532665.1:c.2220_2246del	XP_011530967.1:p.Trp741_Leu749del
XM_011532666.1:c.2148_2174del	XP_011530968.1:p.Trp717_Leu725del
XM_011532667.1:c.2007_2033del	XP_011530969.1:p.Trp670_Leu678del
NM_001320893.1:c.2220_2246del	NP_001307822.1:p.Trp741_Leu749del
NR_135490.1:n.3213_3239del
XM_005264175.5:c.2676_2702del	XP_005264232.1:p.Trp893_Leu901del
XM_005264177.4:c.2007_2033del	XP_005264234.1:p.Trp670_Leu678del
XM_011532662.2:c.2529_2555del	XP_011530964.1:p.Trp844_Leu852del
XM_011532663.2:c.2511_2537del	XP_011530965.1:p.Trp838_Leu846del
XM_011532666.2:c.2148_2174del	XP_011530968.1:p.Trp717_Leu725del
XM_011532667.3:c.2007_2033del	XP_011530969.1:p.Trp670_Leu678del
XM_017003526.1:c.2676_2702del	XP_016859015.1:p.Trp893_Leu901del
XM_017003527.1:c.2007_2033del	XP_016859016.1:p.Trp670_Leu678del
XR_001738657.1:n.2883_2909del
NM_001375819.1:c.2007_2033del	NP_001362748.1:p.Trp670_Leu678del
NR_135490.2:n.3106_3132del
NM_022552.5:c.2676_2702del MANE Select	NP_072046.2:p.Trp893_Leu901del