Canonical Allele Identifier: CA408563168
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436202G>T , CM000682.2:g.32436202G>T GRCh38
NC_000020.10:g.31024005G>T , CM000682.1:g.31024005G>T GRCh37
NC_000020.9:g.30487666G>T NCBI36
NG_027868.1:g.82859G>T , LRG_630:g.82859G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3490G>T MANE Select ENSP00000364839.4:p.Gly1164Ter
ENST00000646985.1:c.3307G>T ENSP00000495053.1:p.Gly1103Ter
ENST00000647223.1:n.5843G>T
ENST00000651418.1:c.1869+1621G>T ENSP00000499150.1:n.1869+1621G>T
ENST00000306058.9:c.3475G>T ENSP00000305119.5:p.Gly1159Ter
ENST00000375687.8:c.3490G>T ENSP00000364839.4:p.Gly1164Ter
ENST00000613218.4:c.3490G>T ENSP00000480487.1:p.Gly1164Ter
ENST00000620121.4:c.3490G>T ENSP00000481978.1:p.Gly1164Ter
NM_015338.5:c.3490G>T , LRG_630t1:c.3490G>T NP_056153.2:p.Gly1164Ter
XM_006723727.2:c.3487G>T XP_006723790.1:p.Gly1163Ter
XM_006723728.2:c.3460G>T XP_006723791.1:p.Gly1154Ter
XM_006723730.2:c.3406G>T XP_006723793.1:p.Gly1136Ter
XM_006723732.2:c.3307G>T XP_006723795.1:p.Gly1103Ter
XM_006723733.1:c.2806G>T XP_006723796.1:p.Gly936Ter
XM_011528647.1:c.3754G>T XP_011526949.1:p.Gly1252Ter
XM_011528648.1:c.3751G>T XP_011526950.1:p.Gly1251Ter
XM_011528649.1:c.3670G>T XP_011526951.1:p.Gly1224Ter
XM_011528650.1:c.3601G>T XP_011526952.1:p.Gly1201Ter
XM_011528651.1:c.3469G>T XP_011526953.1:p.Gly1157Ter
XM_011528652.1:c.3406G>T XP_011526954.1:p.Gly1136Ter
NM_001363734.1:c.3307G>T NP_001350663.1:p.Gly1103Ter
XM_006723727.3:c.3487G>T XP_006723790.1:p.Gly1163Ter
XM_006723728.3:c.3460G>T XP_006723791.1:p.Gly1154Ter
XM_006723730.4:c.3406G>T XP_006723793.1:p.Gly1136Ter
XM_011528648.3:c.3751G>T XP_011526950.1:p.Gly1251Ter
XM_011528652.2:c.3406G>T XP_011526954.1:p.Gly1136Ter
XM_017027704.1:c.3406G>T XP_016883193.1:p.Gly1136Ter
XM_017027705.1:c.3406G>T XP_016883194.1:p.Gly1136Ter
XM_017027706.1:c.3337G>T XP_016883195.1:p.Gly1113Ter
NM_015338.6:c.3490G>T MANE Select NP_056153.2:p.Gly1164Ter