Canonical Allele Identifier: CA2576484113
Gene: ASXL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739285del , CM000680.2:g.33739285del GRCh38
NC_000018.9:g.31319249del , CM000680.1:g.31319249del GRCh37
NC_000018.8:g.29573247del NCBI36
NG_055244.1:g.165709del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1884del ENSP00000513003.1:p.Pro629GlnfsTer?
ENST00000269197.12:c.1881del MANE Select ENSP00000269197.4:p.Pro628GlnfsTer?
ENST00000592288.6:c.*1005del ENSP00000465053.1:n.*1005del
ENST00000592541.6:c.*1540del ENSP00000466655.2:n.*1540del
ENST00000593195.6:c.2093del ENSP00000466073.1:n.2093del
ENST00000642541.1:c.1713del ENSP00000493665.1:p.Pro572GlnfsTer?
ENST00000681521.1:c.1761del ENSP00000506037.1:p.Pro588GlnfsTer?
ENST00000269197.9:c.1881del ENSP00000269197.4:p.Pro628GlnfsTer?
ENST00000592288.5:c.*1005del ENSP00000465053.1:n.*1005del
NM_030632.1:c.1881del NP_085135.1:p.Pro628GlnfsTer?
XM_005258356.1:c.1884del XP_005258413.1:p.Pro629GlnfsTer?
XM_011526205.1:c.1857del XP_011524507.1:p.Pro620GlnfsTer?
XM_011526206.1:c.1803del XP_011524508.1:p.Pro602GlnfsTer?
XM_011526207.1:c.1803del XP_011524509.1:p.Pro602GlnfsTer?
XM_011526208.1:c.1764del XP_011524510.1:p.Pro589GlnfsTer?
XM_011526209.1:c.1713del XP_011524511.1:p.Pro572GlnfsTer?
XM_011526210.1:c.1713del XP_011524512.1:p.Pro572GlnfsTer?
XM_011526211.1:c.1713del XP_011524513.1:p.Pro572GlnfsTer?
XM_011526212.1:c.1713del XP_011524514.1:p.Pro572GlnfsTer?
XM_011526213.1:c.1713del XP_011524515.1:p.Pro572GlnfsTer?
XM_011526214.1:c.1713del XP_011524516.1:p.Pro572GlnfsTer?
NM_030632.2:c.1881del NP_085135.1:p.Pro628GlnfsTer?
XM_011526205.2:c.1857del XP_011524507.1:p.Pro620GlnfsTer?
XM_011526206.2:c.1803del XP_011524508.1:p.Pro602GlnfsTer?
XM_011526213.2:c.1713del XP_011524515.1:p.Pro572GlnfsTer?
XM_017026012.1:c.1803del XP_016881501.1:p.Pro602GlnfsTer?
XM_017026013.1:c.1713del XP_016881502.1:p.Pro572GlnfsTer?
XM_017026014.2:c.1713del XP_016881503.1:p.Pro572GlnfsTer?
XM_024451269.1:c.1713del XP_024307037.1:p.Pro572GlnfsTer?
NM_030632.3:c.1881del MANE Select NP_085135.1:p.Pro628GlnfsTer?