Canonical Allele Identifier: CA402175331
Gene: ASXL3 HGNC NCBI

Linked Data

dbSNP Id: rs2067595825

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33738846A>T , CM000680.2:g.33738846A>T GRCh38
NC_000018.9:g.31318810A>T , CM000680.1:g.31318810A>T GRCh37
NC_000018.8:g.29572808A>T NCBI36
NG_055244.1:g.165270A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1445A>T ENSP00000513003.1:p.Glu482Val
ENST00000269197.12:c.1442A>T MANE Select ENSP00000269197.4:p.Glu481Val
ENST00000592288.6:c.*566A>T ENSP00000465053.1:n.*566A>T
ENST00000592541.6:c.*1101A>T ENSP00000466655.2:n.*1101A>T
ENST00000593195.6:c.1654A>T ENSP00000466073.1:n.1654A>T
ENST00000642541.1:c.1274A>T ENSP00000493665.1:p.Glu425Val
ENST00000681521.1:c.1322A>T ENSP00000506037.1:p.Glu441Val
ENST00000269197.9:c.1442A>T ENSP00000269197.4:p.Glu481Val
ENST00000592288.5:c.*566A>T ENSP00000465053.1:n.*566A>T
NM_030632.1:c.1442A>T NP_085135.1:p.Glu481Val
XM_005258356.1:c.1445A>T XP_005258413.1:p.Glu482Val
XM_011526205.1:c.1418A>T XP_011524507.1:p.Glu473Val
XM_011526206.1:c.1364A>T XP_011524508.1:p.Glu455Val
XM_011526207.1:c.1364A>T XP_011524509.1:p.Glu455Val
XM_011526208.1:c.1325A>T XP_011524510.1:p.Glu442Val
XM_011526209.1:c.1274A>T XP_011524511.1:p.Glu425Val
XM_011526210.1:c.1274A>T XP_011524512.1:p.Glu425Val
XM_011526211.1:c.1274A>T XP_011524513.1:p.Glu425Val
XM_011526212.1:c.1274A>T XP_011524514.1:p.Glu425Val
XM_011526213.1:c.1274A>T XP_011524515.1:p.Glu425Val
XM_011526214.1:c.1274A>T XP_011524516.1:p.Glu425Val
NM_030632.2:c.1442A>T NP_085135.1:p.Glu481Val
XM_011526205.2:c.1418A>T XP_011524507.1:p.Glu473Val
XM_011526206.2:c.1364A>T XP_011524508.1:p.Glu455Val
XM_011526213.2:c.1274A>T XP_011524515.1:p.Glu425Val
XM_017026012.1:c.1364A>T XP_016881501.1:p.Glu455Val
XM_017026013.1:c.1274A>T XP_016881502.1:p.Glu425Val
XM_017026014.2:c.1274A>T XP_016881503.1:p.Glu425Val
XM_024451269.1:c.1274A>T XP_024307037.1:p.Glu425Val
NM_030632.3:c.1442A>T MANE Select NP_085135.1:p.Glu481Val