Canonical Allele Identifier: CA346068024
Gene: DNMT3A HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000474887.6:c.972A>T
ENST00000683393.1:c.1869A>T ENSP00000508654.1:n.1869A>T
ENST00000683760.1:c.2054A>T ENSP00000507765.1:p.Tyr685Phe
ENST00000321117.10:c.2723A>T MANE Select ENSP00000324375.5:p.Tyr908Phe
ENST00000264709.7:c.2723A>T ENSP00000264709.3:p.Tyr908Phe
ENST00000321117.9:c.2723A>T ENSP00000324375.5:p.Tyr908Phe
ENST00000380746.8:c.2156A>T ENSP00000370122.4:p.Tyr719Phe
ENST00000380756.7:c.*576A>T ENSP00000370132.3:n.*576A>T
ENST00000402667.1:c.2054A>T ENSP00000384237.1:p.Tyr685Phe
NM_022552.4:c.2723A>T , LRG_459t1:c.2723A>T NP_072046.2:p.Tyr908Phe
NM_153759.3:c.2156A>T , LRG_459t2:c.2156A>T NP_715640.2:p.Tyr719Phe
NM_175629.2:c.2723A>T , LRG_459t4:c.2723A>T NP_783328.1:p.Tyr908Phe
XM_005264175.3:c.2723A>T XP_005264232.1:p.Tyr908Phe
XM_005264177.3:c.2054A>T XP_005264234.1:p.Tyr685Phe
XM_006711958.2:c.2279A>T XP_006712021.1:p.Tyr760Phe
XM_011532662.1:c.2576A>T XP_011530964.1:p.Tyr859Phe
XM_011532663.1:c.2558A>T XP_011530965.1:p.Tyr853Phe
XM_011532665.1:c.2267A>T XP_011530967.1:p.Tyr756Phe
XM_011532666.1:c.2195A>T XP_011530968.1:p.Tyr732Phe
XM_011532667.1:c.2054A>T XP_011530969.1:p.Tyr685Phe
NM_001320893.1:c.2267A>T NP_001307822.1:p.Tyr756Phe
NR_135490.1:n.3260A>T
XM_005264175.5:c.2723A>T XP_005264232.1:p.Tyr908Phe
XM_005264177.4:c.2054A>T XP_005264234.1:p.Tyr685Phe
XM_011532662.2:c.2576A>T XP_011530964.1:p.Tyr859Phe
XM_011532663.2:c.2558A>T XP_011530965.1:p.Tyr853Phe
XM_011532666.2:c.2195A>T XP_011530968.1:p.Tyr732Phe
XM_011532667.3:c.2054A>T XP_011530969.1:p.Tyr685Phe
XM_017003526.1:c.2723A>T XP_016859015.1:p.Tyr908Phe
XM_017003527.1:c.2054A>T XP_016859016.1:p.Tyr685Phe
XR_001738657.1:n.2930A>T
NM_001375819.1:c.2054A>T NP_001362748.1:p.Tyr685Phe
NR_135490.2:n.3153A>T
NM_022552.5:c.2723A>T MANE Select NP_072046.2:p.Tyr908Phe