Canonical Allele Identifier: CA2294855962
Gene: ASXL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739407C= , CM000680.2:g.33739407C= GRCh38
NC_000018.9:g.31319371C= , CM000680.1:g.31319371C= GRCh37
NC_000018.8:g.29573369C= NCBI36
NG_055244.1:g.165831C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.2006C= ENSP00000513003.1:p.Thr669=
ENST00000269197.12:c.2003C= MANE Select ENSP00000269197.4:p.Thr668=
ENST00000592288.6:c.*1127C= ENSP00000465053.1:n.*1127C=
ENST00000592541.6:c.*1662C= ENSP00000466655.2:n.*1662C=
ENST00000593195.6:c.2215C= ENSP00000466073.1:n.2215C=
ENST00000642541.1:c.1835C= ENSP00000493665.1:p.Thr612=
ENST00000681521.1:c.1883C= ENSP00000506037.1:p.Thr628=
ENST00000269197.9:c.2003C= ENSP00000269197.4:p.Thr668=
ENST00000592288.5:c.*1127C= ENSP00000465053.1:n.*1127C=
NM_030632.1:c.2003C= NP_085135.1:p.Thr668=
XM_005258356.1:c.2006C= XP_005258413.1:p.Thr669=
XM_011526205.1:c.1979C= XP_011524507.1:p.Thr660=
XM_011526206.1:c.1925C= XP_011524508.1:p.Thr642=
XM_011526207.1:c.1925C= XP_011524509.1:p.Thr642=
XM_011526208.1:c.1886C= XP_011524510.1:p.Thr629=
XM_011526209.1:c.1835C= XP_011524511.1:p.Thr612=
XM_011526210.1:c.1835C= XP_011524512.1:p.Thr612=
XM_011526211.1:c.1835C= XP_011524513.1:p.Thr612=
XM_011526212.1:c.1835C= XP_011524514.1:p.Thr612=
XM_011526213.1:c.1835C= XP_011524515.1:p.Thr612=
XM_011526214.1:c.1835C= XP_011524516.1:p.Thr612=
NM_030632.2:c.2003C= NP_085135.1:p.Thr668=
XM_011526205.2:c.1979C= XP_011524507.1:p.Thr660=
XM_011526206.2:c.1925C= XP_011524508.1:p.Thr642=
XM_011526213.2:c.1835C= XP_011524515.1:p.Thr612=
XM_017026012.1:c.1925C= XP_016881501.1:p.Thr642=
XM_017026013.1:c.1835C= XP_016881502.1:p.Thr612=
XM_017026014.2:c.1835C= XP_016881503.1:p.Thr612=
XM_024451269.1:c.1835C= XP_024307037.1:p.Thr612=
NM_030632.3:c.2003C= MANE Select NP_085135.1:p.Thr668=