Canonical Allele Identifier: CA408564290
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436741C>A , CM000682.2:g.32436741C>A GRCh38
NC_000020.10:g.31024544C>A , CM000682.1:g.31024544C>A GRCh37
NC_000020.9:g.30488205C>A NCBI36
NG_027868.1:g.83398C>A , LRG_630:g.83398C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.4029C>A MANE Select ENSP00000364839.4:p.Asn1343Lys
ENST00000646985.1:c.3846C>A ENSP00000495053.1:p.Asn1282Lys
ENST00000647223.1:n.6382C>A
ENST00000651418.1:c.1870-1689C>A ENSP00000499150.1:n.1870-1689C>A
ENST00000306058.9:c.4014C>A ENSP00000305119.5:p.Asn1338Lys
ENST00000375687.8:c.4029C>A ENSP00000364839.4:p.Asn1343Lys
ENST00000613218.4:c.4029C>A ENSP00000480487.1:p.Asn1343Lys
ENST00000620121.4:c.4029C>A ENSP00000481978.1:p.Asn1343Lys
NM_015338.5:c.4029C>A , LRG_630t1:c.4029C>A NP_056153.2:p.Asn1343Lys
XM_006723727.2:c.4026C>A XP_006723790.1:p.Asn1342Lys
XM_006723728.2:c.3999C>A XP_006723791.1:p.Asn1333Lys
XM_006723730.2:c.3945C>A XP_006723793.1:p.Asn1315Lys
XM_006723732.2:c.3846C>A XP_006723795.1:p.Asn1282Lys
XM_006723733.1:c.3345C>A XP_006723796.1:p.Asn1115Lys
XM_011528647.1:c.4293C>A XP_011526949.1:p.Asn1431Lys
XM_011528648.1:c.4290C>A XP_011526950.1:p.Asn1430Lys
XM_011528649.1:c.4209C>A XP_011526951.1:p.Asn1403Lys
XM_011528650.1:c.4140C>A XP_011526952.1:p.Asn1380Lys
XM_011528651.1:c.4008C>A XP_011526953.1:p.Asn1336Lys
XM_011528652.1:c.3945C>A XP_011526954.1:p.Asn1315Lys
NM_001363734.1:c.3846C>A NP_001350663.1:p.Asn1282Lys
XM_006723727.3:c.4026C>A XP_006723790.1:p.Asn1342Lys
XM_006723728.3:c.3999C>A XP_006723791.1:p.Asn1333Lys
XM_006723730.4:c.3945C>A XP_006723793.1:p.Asn1315Lys
XM_011528648.3:c.4290C>A XP_011526950.1:p.Asn1430Lys
XM_011528652.2:c.3945C>A XP_011526954.1:p.Asn1315Lys
XM_017027704.1:c.3945C>A XP_016883193.1:p.Asn1315Lys
XM_017027705.1:c.3945C>A XP_016883194.1:p.Asn1315Lys
XM_017027706.1:c.3876C>A XP_016883195.1:p.Asn1292Lys
NM_015338.6:c.4029C>A MANE Select NP_056153.2:p.Asn1343Lys