Canonical Allele Identifier: CA408562492
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32435878A>T , CM000682.2:g.32435878A>T GRCh38
NC_000020.10:g.31023681A>T , CM000682.1:g.31023681A>T GRCh37
NC_000020.9:g.30487342A>T NCBI36
NG_027868.1:g.82535A>T , LRG_630:g.82535A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3166A>T MANE Select ENSP00000364839.4:p.Thr1056Ser
ENST00000646985.1:c.2983A>T ENSP00000495053.1:p.Thr995Ser
ENST00000647223.1:n.5519A>T
ENST00000651418.1:c.1869+1297A>T ENSP00000499150.1:n.1869+1297A>T
ENST00000306058.9:c.3151A>T ENSP00000305119.5:p.Thr1051Ser
ENST00000375687.8:c.3166A>T ENSP00000364839.4:p.Thr1056Ser
ENST00000613218.4:c.3166A>T ENSP00000480487.1:p.Thr1056Ser
ENST00000620121.4:c.3166A>T ENSP00000481978.1:p.Thr1056Ser
NM_015338.5:c.3166A>T , LRG_630t1:c.3166A>T NP_056153.2:p.Thr1056Ser
XM_006723727.2:c.3163A>T XP_006723790.1:p.Thr1055Ser
XM_006723728.2:c.3136A>T XP_006723791.1:p.Thr1046Ser
XM_006723730.2:c.3082A>T XP_006723793.1:p.Thr1028Ser
XM_006723732.2:c.2983A>T XP_006723795.1:p.Thr995Ser
XM_006723733.1:c.2482A>T XP_006723796.1:p.Thr828Ser
XM_011528647.1:c.3430A>T XP_011526949.1:p.Thr1144Ser
XM_011528648.1:c.3427A>T XP_011526950.1:p.Thr1143Ser
XM_011528649.1:c.3346A>T XP_011526951.1:p.Thr1116Ser
XM_011528650.1:c.3277A>T XP_011526952.1:p.Thr1093Ser
XM_011528651.1:c.3145A>T XP_011526953.1:p.Thr1049Ser
XM_011528652.1:c.3082A>T XP_011526954.1:p.Thr1028Ser
NM_001363734.1:c.2983A>T NP_001350663.1:p.Thr995Ser
XM_006723727.3:c.3163A>T XP_006723790.1:p.Thr1055Ser
XM_006723728.3:c.3136A>T XP_006723791.1:p.Thr1046Ser
XM_006723730.4:c.3082A>T XP_006723793.1:p.Thr1028Ser
XM_011528648.3:c.3427A>T XP_011526950.1:p.Thr1143Ser
XM_011528652.2:c.3082A>T XP_011526954.1:p.Thr1028Ser
XM_017027704.1:c.3082A>T XP_016883193.1:p.Thr1028Ser
XM_017027705.1:c.3082A>T XP_016883194.1:p.Thr1028Ser
XM_017027706.1:c.3013A>T XP_016883195.1:p.Thr1005Ser
NM_015338.6:c.3166A>T MANE Select NP_056153.2:p.Thr1056Ser