Canonical Allele Identifier: CA2576693552

Gene: DNMT3A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25234295del , CM000664.2:g.25234295del	GRCh38
NC_000002.11:g.25457164del , CM000664.1:g.25457164del	GRCh37
NC_000002.10:g.25310668del	NCBI36
NG_029465.2:g.113296del , LRG_459:g.113296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474887.6:c.972del
ENST00000683393.1:c.1869del	ENSP00000508654.1:n.1869del
ENST00000683760.1:c.2054del	ENSP00000507765.1:p.Tyr685PhefsTer14
ENST00000321117.10:c.2723del MANE Select	ENSP00000324375.5:p.Tyr908PhefsTer14
ENST00000264709.7:c.2723del	ENSP00000264709.3:p.Tyr908PhefsTer14
ENST00000321117.9:c.2723del	ENSP00000324375.5:p.Tyr908PhefsTer14
ENST00000380746.8:c.2156del	ENSP00000370122.4:p.Tyr719PhefsTer14
ENST00000380756.7:c.*576del	ENSP00000370132.3:n.*576del
ENST00000402667.1:c.2054del	ENSP00000384237.1:p.Tyr685PhefsTer14
NM_022552.4:c.2723del , LRG_459t1:c.2723del	NP_072046.2:p.Tyr908PhefsTer14
NM_153759.3:c.2156del , LRG_459t2:c.2156del	NP_715640.2:p.Tyr719PhefsTer14
NM_175629.2:c.2723del , LRG_459t4:c.2723del	NP_783328.1:p.Tyr908PhefsTer14
XM_005264175.3:c.2723del	XP_005264232.1:p.Tyr908PhefsTer14
XM_005264177.3:c.2054del	XP_005264234.1:p.Tyr685PhefsTer14
XM_006711958.2:c.2279del	XP_006712021.1:p.Tyr760PhefsTer14
XM_011532662.1:c.2576del	XP_011530964.1:p.Tyr859PhefsTer14
XM_011532663.1:c.2558del	XP_011530965.1:p.Tyr853PhefsTer14
XM_011532665.1:c.2267del	XP_011530967.1:p.Tyr756PhefsTer14
XM_011532666.1:c.2195del	XP_011530968.1:p.Tyr732PhefsTer14
XM_011532667.1:c.2054del	XP_011530969.1:p.Tyr685PhefsTer14
NM_001320893.1:c.2267del	NP_001307822.1:p.Tyr756PhefsTer14
NR_135490.1:n.3260del
XM_005264175.5:c.2723del	XP_005264232.1:p.Tyr908PhefsTer14
XM_005264177.4:c.2054del	XP_005264234.1:p.Tyr685PhefsTer14
XM_011532662.2:c.2576del	XP_011530964.1:p.Tyr859PhefsTer14
XM_011532663.2:c.2558del	XP_011530965.1:p.Tyr853PhefsTer14
XM_011532666.2:c.2195del	XP_011530968.1:p.Tyr732PhefsTer14
XM_011532667.3:c.2054del	XP_011530969.1:p.Tyr685PhefsTer14
XM_017003526.1:c.2723del	XP_016859015.1:p.Tyr908PhefsTer14
XM_017003527.1:c.2054del	XP_016859016.1:p.Tyr685PhefsTer14
XR_001738657.1:n.2930del
NM_001375819.1:c.2054del	NP_001362748.1:p.Tyr685PhefsTer14
NR_135490.2:n.3153del
NM_022552.5:c.2723del MANE Select	NP_072046.2:p.Tyr908PhefsTer14