Canonical Allele Identifier: CA408563058
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436146G>T , CM000682.2:g.32436146G>T GRCh38
NC_000020.10:g.31023949G>T , CM000682.1:g.31023949G>T GRCh37
NC_000020.9:g.30487610G>T NCBI36
NG_027868.1:g.82803G>T , LRG_630:g.82803G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3434G>T MANE Select ENSP00000364839.4:p.Gly1145Val
ENST00000646985.1:c.3251G>T ENSP00000495053.1:p.Gly1084Val
ENST00000647223.1:n.5787G>T
ENST00000651418.1:c.1869+1565G>T ENSP00000499150.1:n.1869+1565G>T
ENST00000306058.9:c.3419G>T ENSP00000305119.5:p.Gly1140Val
ENST00000375687.8:c.3434G>T ENSP00000364839.4:p.Gly1145Val
ENST00000613218.4:c.3434G>T ENSP00000480487.1:p.Gly1145Val
ENST00000620121.4:c.3434G>T ENSP00000481978.1:p.Gly1145Val
NM_015338.5:c.3434G>T , LRG_630t1:c.3434G>T NP_056153.2:p.Gly1145Val
XM_006723727.2:c.3431G>T XP_006723790.1:p.Gly1144Val
XM_006723728.2:c.3404G>T XP_006723791.1:p.Gly1135Val
XM_006723730.2:c.3350G>T XP_006723793.1:p.Gly1117Val
XM_006723732.2:c.3251G>T XP_006723795.1:p.Gly1084Val
XM_006723733.1:c.2750G>T XP_006723796.1:p.Gly917Val
XM_011528647.1:c.3698G>T XP_011526949.1:p.Gly1233Val
XM_011528648.1:c.3695G>T XP_011526950.1:p.Gly1232Val
XM_011528649.1:c.3614G>T XP_011526951.1:p.Gly1205Val
XM_011528650.1:c.3545G>T XP_011526952.1:p.Gly1182Val
XM_011528651.1:c.3413G>T XP_011526953.1:p.Gly1138Val
XM_011528652.1:c.3350G>T XP_011526954.1:p.Gly1117Val
NM_001363734.1:c.3251G>T NP_001350663.1:p.Gly1084Val
XM_006723727.3:c.3431G>T XP_006723790.1:p.Gly1144Val
XM_006723728.3:c.3404G>T XP_006723791.1:p.Gly1135Val
XM_006723730.4:c.3350G>T XP_006723793.1:p.Gly1117Val
XM_011528648.3:c.3695G>T XP_011526950.1:p.Gly1232Val
XM_011528652.2:c.3350G>T XP_011526954.1:p.Gly1117Val
XM_017027704.1:c.3350G>T XP_016883193.1:p.Gly1117Val
XM_017027705.1:c.3350G>T XP_016883194.1:p.Gly1117Val
XM_017027706.1:c.3281G>T XP_016883195.1:p.Gly1094Val
NM_015338.6:c.3434G>T MANE Select NP_056153.2:p.Gly1145Val