Canonical Allele Identifier: CA2360293615
Gene: ASXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436260A= , CM000682.2:g.32436260A= GRCh38
NC_000020.10:g.31024063A= , CM000682.1:g.31024063A= GRCh37
NC_000020.9:g.30487724A= NCBI36
NG_027868.1:g.82917A= , LRG_630:g.82917A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375687.10:c.3548A= MANE Select ENSP00000364839.4:p.Glu1183=
ENST00000646985.1:c.3365A= ENSP00000495053.1:p.Glu1122=
ENST00000647223.1:n.5901A=
ENST00000651418.1:c.1869+1679A= ENSP00000499150.1:n.1869+1679A=
ENST00000306058.9:c.3533A= ENSP00000305119.5:p.Glu1178=
ENST00000375687.8:c.3548A= ENSP00000364839.4:p.Glu1183=
ENST00000613218.4:c.3548A= ENSP00000480487.1:p.Glu1183=
ENST00000620121.4:c.3548A= ENSP00000481978.1:p.Glu1183=
NM_015338.5:c.3548A= , LRG_630t1:c.3548A= NP_056153.2:p.Glu1183=
XM_006723727.2:c.3545A= XP_006723790.1:p.Glu1182=
XM_006723728.2:c.3518A= XP_006723791.1:p.Glu1173=
XM_006723730.2:c.3464A= XP_006723793.1:p.Glu1155=
XM_006723732.2:c.3365A= XP_006723795.1:p.Glu1122=
XM_006723733.1:c.2864A= XP_006723796.1:p.Glu955=
XM_011528647.1:c.3812A= XP_011526949.1:p.Glu1271=
XM_011528648.1:c.3809A= XP_011526950.1:p.Glu1270=
XM_011528649.1:c.3728A= XP_011526951.1:p.Glu1243=
XM_011528650.1:c.3659A= XP_011526952.1:p.Glu1220=
XM_011528651.1:c.3527A= XP_011526953.1:p.Glu1176=
XM_011528652.1:c.3464A= XP_011526954.1:p.Glu1155=
NM_001363734.1:c.3365A= NP_001350663.1:p.Glu1122=
XM_006723727.3:c.3545A= XP_006723790.1:p.Glu1182=
XM_006723728.3:c.3518A= XP_006723791.1:p.Glu1173=
XM_006723730.4:c.3464A= XP_006723793.1:p.Glu1155=
XM_011528648.3:c.3809A= XP_011526950.1:p.Glu1270=
XM_011528652.2:c.3464A= XP_011526954.1:p.Glu1155=
XM_017027704.1:c.3464A= XP_016883193.1:p.Glu1155=
XM_017027705.1:c.3464A= XP_016883194.1:p.Glu1155=
XM_017027706.1:c.3395A= XP_016883195.1:p.Glu1132=
NM_015338.6:c.3548A= MANE Select NP_056153.2:p.Glu1183=