Canonical Allele Identifier: CA408562622
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32435941C>A , CM000682.2:g.32435941C>A GRCh38
NC_000020.10:g.31023744C>A , CM000682.1:g.31023744C>A GRCh37
NC_000020.9:g.30487405C>A NCBI36
NG_027868.1:g.82598C>A , LRG_630:g.82598C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3229C>A MANE Select ENSP00000364839.4:p.Pro1077Thr
ENST00000646985.1:c.3046C>A ENSP00000495053.1:p.Pro1016Thr
ENST00000647223.1:n.5582C>A
ENST00000651418.1:c.1869+1360C>A ENSP00000499150.1:n.1869+1360C>A
ENST00000306058.9:c.3214C>A ENSP00000305119.5:p.Pro1072Thr
ENST00000375687.8:c.3229C>A ENSP00000364839.4:p.Pro1077Thr
ENST00000613218.4:c.3229C>A ENSP00000480487.1:p.Pro1077Thr
ENST00000620121.4:c.3229C>A ENSP00000481978.1:p.Pro1077Thr
NM_015338.5:c.3229C>A , LRG_630t1:c.3229C>A NP_056153.2:p.Pro1077Thr
XM_006723727.2:c.3226C>A XP_006723790.1:p.Pro1076Thr
XM_006723728.2:c.3199C>A XP_006723791.1:p.Pro1067Thr
XM_006723730.2:c.3145C>A XP_006723793.1:p.Pro1049Thr
XM_006723732.2:c.3046C>A XP_006723795.1:p.Pro1016Thr
XM_006723733.1:c.2545C>A XP_006723796.1:p.Pro849Thr
XM_011528647.1:c.3493C>A XP_011526949.1:p.Pro1165Thr
XM_011528648.1:c.3490C>A XP_011526950.1:p.Pro1164Thr
XM_011528649.1:c.3409C>A XP_011526951.1:p.Pro1137Thr
XM_011528650.1:c.3340C>A XP_011526952.1:p.Pro1114Thr
XM_011528651.1:c.3208C>A XP_011526953.1:p.Pro1070Thr
XM_011528652.1:c.3145C>A XP_011526954.1:p.Pro1049Thr
NM_001363734.1:c.3046C>A NP_001350663.1:p.Pro1016Thr
XM_006723727.3:c.3226C>A XP_006723790.1:p.Pro1076Thr
XM_006723728.3:c.3199C>A XP_006723791.1:p.Pro1067Thr
XM_006723730.4:c.3145C>A XP_006723793.1:p.Pro1049Thr
XM_011528648.3:c.3490C>A XP_011526950.1:p.Pro1164Thr
XM_011528652.2:c.3145C>A XP_011526954.1:p.Pro1049Thr
XM_017027704.1:c.3145C>A XP_016883193.1:p.Pro1049Thr
XM_017027705.1:c.3145C>A XP_016883194.1:p.Pro1049Thr
XM_017027706.1:c.3076C>A XP_016883195.1:p.Pro1026Thr
NM_015338.6:c.3229C>A MANE Select NP_056153.2:p.Pro1077Thr