Canonical Allele Identifier: CA16620686
Gene: ASXL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 419279
dbSNP Id: rs1064793765

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33743212C>T , CM000680.2:g.33743212C>T GRCh38
NC_000018.9:g.31323176C>T , CM000680.1:g.31323176C>T GRCh37
NC_000018.8:g.29577174C>T NCBI36
NG_055244.1:g.169636C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696964.1:c.3367C>T ENSP00000513003.1:p.Gln1123Ter
ENST00000269197.12:c.3364C>T MANE Select ENSP00000269197.4:p.Gln1122Ter
ENST00000592288.6:c.*2488C>T ENSP00000465053.1:n.*2488C>T
ENST00000592541.6:c.*3023C>T ENSP00000466655.2:n.*3023C>T
ENST00000593195.6:c.3576C>T ENSP00000466073.1:n.3576C>T
ENST00000642541.1:c.3196C>T ENSP00000493665.1:p.Gln1066Ter
ENST00000681521.1:c.3244C>T ENSP00000506037.1:p.Gln1082Ter
ENST00000269197.9:c.3364C>T ENSP00000269197.4:p.Gln1122Ter
ENST00000592288.5:c.*2488C>T ENSP00000465053.1:n.*2488C>T
NM_030632.1:c.3364C>T NP_085135.1:p.Gln1122Ter
XM_005258356.1:c.3367C>T XP_005258413.1:p.Gln1123Ter
XM_011526205.1:c.3340C>T XP_011524507.1:p.Gln1114Ter
XM_011526206.1:c.3286C>T XP_011524508.1:p.Gln1096Ter
XM_011526207.1:c.3286C>T XP_011524509.1:p.Gln1096Ter
XM_011526208.1:c.3247C>T XP_011524510.1:p.Gln1083Ter
XM_011526209.1:c.3196C>T XP_011524511.1:p.Gln1066Ter
XM_011526210.1:c.3196C>T XP_011524512.1:p.Gln1066Ter
XM_011526211.1:c.3196C>T XP_011524513.1:p.Gln1066Ter
XM_011526212.1:c.3196C>T XP_011524514.1:p.Gln1066Ter
XM_011526213.1:c.3196C>T XP_011524515.1:p.Gln1066Ter
XM_011526214.1:c.3196C>T XP_011524516.1:p.Gln1066Ter
XM_011526215.1:c.328C>T XP_011524517.1:p.Gln110Ter
NM_030632.2:c.3364C>T NP_085135.1:p.Gln1122Ter
XM_011526205.2:c.3340C>T XP_011524507.1:p.Gln1114Ter
XM_011526206.2:c.3286C>T XP_011524508.1:p.Gln1096Ter
XM_011526213.2:c.3196C>T XP_011524515.1:p.Gln1066Ter
XM_017026012.1:c.3286C>T XP_016881501.1:p.Gln1096Ter
XM_017026013.1:c.3196C>T XP_016881502.1:p.Gln1066Ter
XM_017026014.2:c.3196C>T XP_016881503.1:p.Gln1066Ter
XM_024451269.1:c.3196C>T XP_024307037.1:p.Gln1066Ter
NM_030632.3:c.3364C>T MANE Select NP_085135.1:p.Gln1122Ter