Canonical Allele Identifier: CA408564245
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436719G>A , CM000682.2:g.32436719G>A GRCh38
NC_000020.10:g.31024522G>A , CM000682.1:g.31024522G>A GRCh37
NC_000020.9:g.30488183G>A NCBI36
NG_027868.1:g.83376G>A , LRG_630:g.83376G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.4007G>A MANE Select ENSP00000364839.4:p.Gly1336Glu
ENST00000646985.1:c.3824G>A ENSP00000495053.1:p.Gly1275Glu
ENST00000647223.1:n.6360G>A
ENST00000651418.1:c.1870-1711G>A ENSP00000499150.1:n.1870-1711G>A
ENST00000306058.9:c.3992G>A ENSP00000305119.5:p.Gly1331Glu
ENST00000375687.8:c.4007G>A ENSP00000364839.4:p.Gly1336Glu
ENST00000613218.4:c.4007G>A ENSP00000480487.1:p.Gly1336Glu
ENST00000620121.4:c.4007G>A ENSP00000481978.1:p.Gly1336Glu
NM_015338.5:c.4007G>A , LRG_630t1:c.4007G>A NP_056153.2:p.Gly1336Glu
XM_006723727.2:c.4004G>A XP_006723790.1:p.Gly1335Glu
XM_006723728.2:c.3977G>A XP_006723791.1:p.Gly1326Glu
XM_006723730.2:c.3923G>A XP_006723793.1:p.Gly1308Glu
XM_006723732.2:c.3824G>A XP_006723795.1:p.Gly1275Glu
XM_006723733.1:c.3323G>A XP_006723796.1:p.Gly1108Glu
XM_011528647.1:c.4271G>A XP_011526949.1:p.Gly1424Glu
XM_011528648.1:c.4268G>A XP_011526950.1:p.Gly1423Glu
XM_011528649.1:c.4187G>A XP_011526951.1:p.Gly1396Glu
XM_011528650.1:c.4118G>A XP_011526952.1:p.Gly1373Glu
XM_011528651.1:c.3986G>A XP_011526953.1:p.Gly1329Glu
XM_011528652.1:c.3923G>A XP_011526954.1:p.Gly1308Glu
NM_001363734.1:c.3824G>A NP_001350663.1:p.Gly1275Glu
XM_006723727.3:c.4004G>A XP_006723790.1:p.Gly1335Glu
XM_006723728.3:c.3977G>A XP_006723791.1:p.Gly1326Glu
XM_006723730.4:c.3923G>A XP_006723793.1:p.Gly1308Glu
XM_011528648.3:c.4268G>A XP_011526950.1:p.Gly1423Glu
XM_011528652.2:c.3923G>A XP_011526954.1:p.Gly1308Glu
XM_017027704.1:c.3923G>A XP_016883193.1:p.Gly1308Glu
XM_017027705.1:c.3923G>A XP_016883194.1:p.Gly1308Glu
XM_017027706.1:c.3854G>A XP_016883195.1:p.Gly1285Glu
NM_015338.6:c.4007G>A MANE Select NP_056153.2:p.Gly1336Glu