Canonical Allele Identifier: CA402176623
Gene: ASXL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.33739263G>A , CM000680.2:g.33739263G>A GRCh38
NC_000018.9:g.31319227G>A , CM000680.1:g.31319227G>A GRCh37
NC_000018.8:g.29573225G>A NCBI36
NG_055244.1:g.165687G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696964.1:c.1862G>A ENSP00000513003.1:p.Gly621Glu
ENST00000269197.12:c.1859G>A MANE Select ENSP00000269197.4:p.Gly620Glu
ENST00000592288.6:c.*983G>A ENSP00000465053.1:n.*983G>A
ENST00000592541.6:c.*1518G>A ENSP00000466655.2:n.*1518G>A
ENST00000593195.6:c.2071G>A ENSP00000466073.1:n.2071G>A
ENST00000642541.1:c.1691G>A ENSP00000493665.1:p.Gly564Glu
ENST00000681521.1:c.1739G>A ENSP00000506037.1:p.Gly580Glu
ENST00000269197.9:c.1859G>A ENSP00000269197.4:p.Gly620Glu
ENST00000592288.5:c.*983G>A ENSP00000465053.1:n.*983G>A
NM_030632.1:c.1859G>A NP_085135.1:p.Gly620Glu
XM_005258356.1:c.1862G>A XP_005258413.1:p.Gly621Glu
XM_011526205.1:c.1835G>A XP_011524507.1:p.Gly612Glu
XM_011526206.1:c.1781G>A XP_011524508.1:p.Gly594Glu
XM_011526207.1:c.1781G>A XP_011524509.1:p.Gly594Glu
XM_011526208.1:c.1742G>A XP_011524510.1:p.Gly581Glu
XM_011526209.1:c.1691G>A XP_011524511.1:p.Gly564Glu
XM_011526210.1:c.1691G>A XP_011524512.1:p.Gly564Glu
XM_011526211.1:c.1691G>A XP_011524513.1:p.Gly564Glu
XM_011526212.1:c.1691G>A XP_011524514.1:p.Gly564Glu
XM_011526213.1:c.1691G>A XP_011524515.1:p.Gly564Glu
XM_011526214.1:c.1691G>A XP_011524516.1:p.Gly564Glu
NM_030632.2:c.1859G>A NP_085135.1:p.Gly620Glu
XM_011526205.2:c.1835G>A XP_011524507.1:p.Gly612Glu
XM_011526206.2:c.1781G>A XP_011524508.1:p.Gly594Glu
XM_011526213.2:c.1691G>A XP_011524515.1:p.Gly564Glu
XM_017026012.1:c.1781G>A XP_016881501.1:p.Gly594Glu
XM_017026013.1:c.1691G>A XP_016881502.1:p.Gly564Glu
XM_017026014.2:c.1691G>A XP_016881503.1:p.Gly564Glu
XM_024451269.1:c.1691G>A XP_024307037.1:p.Gly564Glu
NM_030632.3:c.1859G>A MANE Select NP_085135.1:p.Gly620Glu