Canonical Allele Identifier: CA408563466
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436343G>A , CM000682.2:g.32436343G>A GRCh38
NC_000020.10:g.31024146G>A , CM000682.1:g.31024146G>A GRCh37
NC_000020.9:g.30487807G>A NCBI36
NG_027868.1:g.83000G>A , LRG_630:g.83000G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3631G>A MANE Select ENSP00000364839.4:p.Asp1211Asn
ENST00000646985.1:c.3448G>A ENSP00000495053.1:p.Asp1150Asn
ENST00000647223.1:n.5984G>A
ENST00000651418.1:c.1869+1762G>A ENSP00000499150.1:n.1869+1762G>A
ENST00000306058.9:c.3616G>A ENSP00000305119.5:p.Asp1206Asn
ENST00000375687.8:c.3631G>A ENSP00000364839.4:p.Asp1211Asn
ENST00000613218.4:c.3631G>A ENSP00000480487.1:p.Asp1211Asn
ENST00000620121.4:c.3631G>A ENSP00000481978.1:p.Asp1211Asn
NM_015338.5:c.3631G>A , LRG_630t1:c.3631G>A NP_056153.2:p.Asp1211Asn
XM_006723727.2:c.3628G>A XP_006723790.1:p.Asp1210Asn
XM_006723728.2:c.3601G>A XP_006723791.1:p.Asp1201Asn
XM_006723730.2:c.3547G>A XP_006723793.1:p.Asp1183Asn
XM_006723732.2:c.3448G>A XP_006723795.1:p.Asp1150Asn
XM_006723733.1:c.2947G>A XP_006723796.1:p.Asp983Asn
XM_011528647.1:c.3895G>A XP_011526949.1:p.Asp1299Asn
XM_011528648.1:c.3892G>A XP_011526950.1:p.Asp1298Asn
XM_011528649.1:c.3811G>A XP_011526951.1:p.Asp1271Asn
XM_011528650.1:c.3742G>A XP_011526952.1:p.Asp1248Asn
XM_011528651.1:c.3610G>A XP_011526953.1:p.Asp1204Asn
XM_011528652.1:c.3547G>A XP_011526954.1:p.Asp1183Asn
NM_001363734.1:c.3448G>A NP_001350663.1:p.Asp1150Asn
XM_006723727.3:c.3628G>A XP_006723790.1:p.Asp1210Asn
XM_006723728.3:c.3601G>A XP_006723791.1:p.Asp1201Asn
XM_006723730.4:c.3547G>A XP_006723793.1:p.Asp1183Asn
XM_011528648.3:c.3892G>A XP_011526950.1:p.Asp1298Asn
XM_011528652.2:c.3547G>A XP_011526954.1:p.Asp1183Asn
XM_017027704.1:c.3547G>A XP_016883193.1:p.Asp1183Asn
XM_017027705.1:c.3547G>A XP_016883194.1:p.Asp1183Asn
XM_017027706.1:c.3478G>A XP_016883195.1:p.Asp1160Asn
NM_015338.6:c.3631G>A MANE Select NP_056153.2:p.Asp1211Asn