Canonical Allele Identifier: CA408562855
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436052G>A , CM000682.2:g.32436052G>A GRCh38
NC_000020.10:g.31023855G>A , CM000682.1:g.31023855G>A GRCh37
NC_000020.9:g.30487516G>A NCBI36
NG_027868.1:g.82709G>A , LRG_630:g.82709G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3340G>A MANE Select ENSP00000364839.4:p.Gly1114Ser
ENST00000646985.1:c.3157G>A ENSP00000495053.1:p.Gly1053Ser
ENST00000647223.1:n.5693G>A
ENST00000651418.1:c.1869+1471G>A ENSP00000499150.1:n.1869+1471G>A
ENST00000306058.9:c.3325G>A ENSP00000305119.5:p.Gly1109Ser
ENST00000375687.8:c.3340G>A ENSP00000364839.4:p.Gly1114Ser
ENST00000613218.4:c.3340G>A ENSP00000480487.1:p.Gly1114Ser
ENST00000620121.4:c.3340G>A ENSP00000481978.1:p.Gly1114Ser
NM_015338.5:c.3340G>A , LRG_630t1:c.3340G>A NP_056153.2:p.Gly1114Ser
XM_006723727.2:c.3337G>A XP_006723790.1:p.Gly1113Ser
XM_006723728.2:c.3310G>A XP_006723791.1:p.Gly1104Ser
XM_006723730.2:c.3256G>A XP_006723793.1:p.Gly1086Ser
XM_006723732.2:c.3157G>A XP_006723795.1:p.Gly1053Ser
XM_006723733.1:c.2656G>A XP_006723796.1:p.Gly886Ser
XM_011528647.1:c.3604G>A XP_011526949.1:p.Gly1202Ser
XM_011528648.1:c.3601G>A XP_011526950.1:p.Gly1201Ser
XM_011528649.1:c.3520G>A XP_011526951.1:p.Gly1174Ser
XM_011528650.1:c.3451G>A XP_011526952.1:p.Gly1151Ser
XM_011528651.1:c.3319G>A XP_011526953.1:p.Gly1107Ser
XM_011528652.1:c.3256G>A XP_011526954.1:p.Gly1086Ser
NM_001363734.1:c.3157G>A NP_001350663.1:p.Gly1053Ser
XM_006723727.3:c.3337G>A XP_006723790.1:p.Gly1113Ser
XM_006723728.3:c.3310G>A XP_006723791.1:p.Gly1104Ser
XM_006723730.4:c.3256G>A XP_006723793.1:p.Gly1086Ser
XM_011528648.3:c.3601G>A XP_011526950.1:p.Gly1201Ser
XM_011528652.2:c.3256G>A XP_011526954.1:p.Gly1086Ser
XM_017027704.1:c.3256G>A XP_016883193.1:p.Gly1086Ser
XM_017027705.1:c.3256G>A XP_016883194.1:p.Gly1086Ser
XM_017027706.1:c.3187G>A XP_016883195.1:p.Gly1063Ser
NM_015338.6:c.3340G>A MANE Select NP_056153.2:p.Gly1114Ser