Canonical Allele Identifier: CA2360293613
Gene: ASXL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436253A= , CM000682.2:g.32436253A= GRCh38
NC_000020.10:g.31024056A= , CM000682.1:g.31024056A= GRCh37
NC_000020.9:g.30487717A= NCBI36
NG_027868.1:g.82910A= , LRG_630:g.82910A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375687.10:c.3541A= MANE Select ENSP00000364839.4:p.Ser1181=
ENST00000646985.1:c.3358A= ENSP00000495053.1:p.Ser1120=
ENST00000647223.1:n.5894A=
ENST00000651418.1:c.1869+1672A= ENSP00000499150.1:n.1869+1672A=
ENST00000306058.9:c.3526A= ENSP00000305119.5:p.Ser1176=
ENST00000375687.8:c.3541A= ENSP00000364839.4:p.Ser1181=
ENST00000613218.4:c.3541A= ENSP00000480487.1:p.Ser1181=
ENST00000620121.4:c.3541A= ENSP00000481978.1:p.Ser1181=
NM_015338.5:c.3541A= , LRG_630t1:c.3541A= NP_056153.2:p.Ser1181=
XM_006723727.2:c.3538A= XP_006723790.1:p.Ser1180=
XM_006723728.2:c.3511A= XP_006723791.1:p.Ser1171=
XM_006723730.2:c.3457A= XP_006723793.1:p.Ser1153=
XM_006723732.2:c.3358A= XP_006723795.1:p.Ser1120=
XM_006723733.1:c.2857A= XP_006723796.1:p.Ser953=
XM_011528647.1:c.3805A= XP_011526949.1:p.Ser1269=
XM_011528648.1:c.3802A= XP_011526950.1:p.Ser1268=
XM_011528649.1:c.3721A= XP_011526951.1:p.Ser1241=
XM_011528650.1:c.3652A= XP_011526952.1:p.Ser1218=
XM_011528651.1:c.3520A= XP_011526953.1:p.Ser1174=
XM_011528652.1:c.3457A= XP_011526954.1:p.Ser1153=
NM_001363734.1:c.3358A= NP_001350663.1:p.Ser1120=
XM_006723727.3:c.3538A= XP_006723790.1:p.Ser1180=
XM_006723728.3:c.3511A= XP_006723791.1:p.Ser1171=
XM_006723730.4:c.3457A= XP_006723793.1:p.Ser1153=
XM_011528648.3:c.3802A= XP_011526950.1:p.Ser1268=
XM_011528652.2:c.3457A= XP_011526954.1:p.Ser1153=
XM_017027704.1:c.3457A= XP_016883193.1:p.Ser1153=
XM_017027705.1:c.3457A= XP_016883194.1:p.Ser1153=
XM_017027706.1:c.3388A= XP_016883195.1:p.Ser1130=
NM_015338.6:c.3541A= MANE Select NP_056153.2:p.Ser1181=