Canonical Allele Identifier: CA645612973
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436654del , CM000682.2:g.32436654del GRCh38
NC_000020.10:g.31024457del , CM000682.1:g.31024457del GRCh37
NC_000020.9:g.30488118del NCBI36
NG_027868.1:g.83311del , LRG_630:g.83311del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3942del MANE Select ENSP00000364839.4:p.Gln1315SerfsTer?
ENST00000646985.1:c.3759del ENSP00000495053.1:p.Gln1254SerfsTer?
ENST00000647223.1:n.6295del
ENST00000651418.1:c.1870-1776del ENSP00000499150.1:n.1870-1776del
ENST00000306058.9:c.3927del ENSP00000305119.5:p.Gln1310SerfsTer?
ENST00000375687.8:c.3942del ENSP00000364839.4:p.Gln1315SerfsTer?
ENST00000613218.4:c.3942del ENSP00000480487.1:p.Gln1315SerfsTer?
ENST00000620121.4:c.3942del ENSP00000481978.1:p.Gln1315SerfsTer?
NM_015338.5:c.3942del , LRG_630t1:c.3942del NP_056153.2:p.Gln1315SerfsTer?
XM_006723727.2:c.3939del XP_006723790.1:p.Gln1314SerfsTer?
XM_006723728.2:c.3912del XP_006723791.1:p.Gln1305SerfsTer?
XM_006723730.2:c.3858del XP_006723793.1:p.Gln1287SerfsTer?
XM_006723732.2:c.3759del XP_006723795.1:p.Gln1254SerfsTer?
XM_006723733.1:c.3258del XP_006723796.1:p.Gln1087SerfsTer?
XM_011528647.1:c.4206del XP_011526949.1:p.Gln1403SerfsTer?
XM_011528648.1:c.4203del XP_011526950.1:p.Gln1402SerfsTer?
XM_011528649.1:c.4122del XP_011526951.1:p.Gln1375SerfsTer?
XM_011528650.1:c.4053del XP_011526952.1:p.Gln1352SerfsTer?
XM_011528651.1:c.3921del XP_011526953.1:p.Gln1308SerfsTer?
XM_011528652.1:c.3858del XP_011526954.1:p.Gln1287SerfsTer?
NM_001363734.1:c.3759del NP_001350663.1:p.Gln1254SerfsTer?
XM_006723727.3:c.3939del XP_006723790.1:p.Gln1314SerfsTer?
XM_006723728.3:c.3912del XP_006723791.1:p.Gln1305SerfsTer?
XM_006723730.4:c.3858del XP_006723793.1:p.Gln1287SerfsTer?
XM_011528648.3:c.4203del XP_011526950.1:p.Gln1402SerfsTer?
XM_011528652.2:c.3858del XP_011526954.1:p.Gln1287SerfsTer?
XM_017027704.1:c.3858del XP_016883193.1:p.Gln1287SerfsTer?
XM_017027705.1:c.3858del XP_016883194.1:p.Gln1287SerfsTer?
XM_017027706.1:c.3789del XP_016883195.1:p.Gln1264SerfsTer?
NM_015338.6:c.3942del MANE Select NP_056153.2:p.Gln1315SerfsTer?