Canonical Allele Identifier: CA408564357
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436774A>C , CM000682.2:g.32436774A>C GRCh38
NC_000020.10:g.31024577A>C , CM000682.1:g.31024577A>C GRCh37
NC_000020.9:g.30488238A>C NCBI36
NG_027868.1:g.83431A>C , LRG_630:g.83431A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.4062A>C MANE Select ENSP00000364839.4:p.Glu1354Asp
ENST00000646985.1:c.3879A>C ENSP00000495053.1:p.Glu1293Asp
ENST00000647223.1:n.6415A>C
ENST00000651418.1:c.1870-1656A>C ENSP00000499150.1:n.1870-1656A>C
ENST00000306058.9:c.4047A>C ENSP00000305119.5:p.Glu1349Asp
ENST00000375687.8:c.4062A>C ENSP00000364839.4:p.Glu1354Asp
ENST00000613218.4:c.4062A>C ENSP00000480487.1:p.Glu1354Asp
ENST00000620121.4:c.4062A>C ENSP00000481978.1:p.Glu1354Asp
NM_015338.5:c.4062A>C , LRG_630t1:c.4062A>C NP_056153.2:p.Glu1354Asp
XM_006723727.2:c.4059A>C XP_006723790.1:p.Glu1353Asp
XM_006723728.2:c.4032A>C XP_006723791.1:p.Glu1344Asp
XM_006723730.2:c.3978A>C XP_006723793.1:p.Glu1326Asp
XM_006723732.2:c.3879A>C XP_006723795.1:p.Glu1293Asp
XM_006723733.1:c.3378A>C XP_006723796.1:p.Glu1126Asp
XM_011528647.1:c.4326A>C XP_011526949.1:p.Glu1442Asp
XM_011528648.1:c.4323A>C XP_011526950.1:p.Glu1441Asp
XM_011528649.1:c.4242A>C XP_011526951.1:p.Glu1414Asp
XM_011528650.1:c.4173A>C XP_011526952.1:p.Glu1391Asp
XM_011528651.1:c.4041A>C XP_011526953.1:p.Glu1347Asp
XM_011528652.1:c.3978A>C XP_011526954.1:p.Glu1326Asp
NM_001363734.1:c.3879A>C NP_001350663.1:p.Glu1293Asp
XM_006723727.3:c.4059A>C XP_006723790.1:p.Glu1353Asp
XM_006723728.3:c.4032A>C XP_006723791.1:p.Glu1344Asp
XM_006723730.4:c.3978A>C XP_006723793.1:p.Glu1326Asp
XM_011528648.3:c.4323A>C XP_011526950.1:p.Glu1441Asp
XM_011528652.2:c.3978A>C XP_011526954.1:p.Glu1326Asp
XM_017027704.1:c.3978A>C XP_016883193.1:p.Glu1326Asp
XM_017027705.1:c.3978A>C XP_016883194.1:p.Glu1326Asp
XM_017027706.1:c.3909A>C XP_016883195.1:p.Glu1303Asp
NM_015338.6:c.4062A>C MANE Select NP_056153.2:p.Glu1354Asp