Canonical Allele Identifier: CA408562537
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32435900A>C , CM000682.2:g.32435900A>C GRCh38
NC_000020.10:g.31023703A>C , CM000682.1:g.31023703A>C GRCh37
NC_000020.9:g.30487364A>C NCBI36
NG_027868.1:g.82557A>C , LRG_630:g.82557A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3188A>C MANE Select ENSP00000364839.4:p.Gln1063Pro
ENST00000646985.1:c.3005A>C ENSP00000495053.1:p.Gln1002Pro
ENST00000647223.1:n.5541A>C
ENST00000651418.1:c.1869+1319A>C ENSP00000499150.1:n.1869+1319A>C
ENST00000306058.9:c.3173A>C ENSP00000305119.5:p.Gln1058Pro
ENST00000375687.8:c.3188A>C ENSP00000364839.4:p.Gln1063Pro
ENST00000613218.4:c.3188A>C ENSP00000480487.1:p.Gln1063Pro
ENST00000620121.4:c.3188A>C ENSP00000481978.1:p.Gln1063Pro
NM_015338.5:c.3188A>C , LRG_630t1:c.3188A>C NP_056153.2:p.Gln1063Pro
XM_006723727.2:c.3185A>C XP_006723790.1:p.Gln1062Pro
XM_006723728.2:c.3158A>C XP_006723791.1:p.Gln1053Pro
XM_006723730.2:c.3104A>C XP_006723793.1:p.Gln1035Pro
XM_006723732.2:c.3005A>C XP_006723795.1:p.Gln1002Pro
XM_006723733.1:c.2504A>C XP_006723796.1:p.Gln835Pro
XM_011528647.1:c.3452A>C XP_011526949.1:p.Gln1151Pro
XM_011528648.1:c.3449A>C XP_011526950.1:p.Gln1150Pro
XM_011528649.1:c.3368A>C XP_011526951.1:p.Gln1123Pro
XM_011528650.1:c.3299A>C XP_011526952.1:p.Gln1100Pro
XM_011528651.1:c.3167A>C XP_011526953.1:p.Gln1056Pro
XM_011528652.1:c.3104A>C XP_011526954.1:p.Gln1035Pro
NM_001363734.1:c.3005A>C NP_001350663.1:p.Gln1002Pro
XM_006723727.3:c.3185A>C XP_006723790.1:p.Gln1062Pro
XM_006723728.3:c.3158A>C XP_006723791.1:p.Gln1053Pro
XM_006723730.4:c.3104A>C XP_006723793.1:p.Gln1035Pro
XM_011528648.3:c.3449A>C XP_011526950.1:p.Gln1150Pro
XM_011528652.2:c.3104A>C XP_011526954.1:p.Gln1035Pro
XM_017027704.1:c.3104A>C XP_016883193.1:p.Gln1035Pro
XM_017027705.1:c.3104A>C XP_016883194.1:p.Gln1035Pro
XM_017027706.1:c.3035A>C XP_016883195.1:p.Gln1012Pro
NM_015338.6:c.3188A>C MANE Select NP_056153.2:p.Gln1063Pro