Canonical Allele Identifier: CA408564241
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32436717T>G , CM000682.2:g.32436717T>G GRCh38
NC_000020.10:g.31024520T>G , CM000682.1:g.31024520T>G GRCh37
NC_000020.9:g.30488181T>G NCBI36
NG_027868.1:g.83374T>G , LRG_630:g.83374T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.4005T>G MANE Select ENSP00000364839.4:p.Ser1335Arg
ENST00000646985.1:c.3822T>G ENSP00000495053.1:p.Ser1274Arg
ENST00000647223.1:n.6358T>G
ENST00000651418.1:c.1870-1713T>G ENSP00000499150.1:n.1870-1713T>G
ENST00000306058.9:c.3990T>G ENSP00000305119.5:p.Ser1330Arg
ENST00000375687.8:c.4005T>G ENSP00000364839.4:p.Ser1335Arg
ENST00000613218.4:c.4005T>G ENSP00000480487.1:p.Ser1335Arg
ENST00000620121.4:c.4005T>G ENSP00000481978.1:p.Ser1335Arg
NM_015338.5:c.4005T>G , LRG_630t1:c.4005T>G NP_056153.2:p.Ser1335Arg
XM_006723727.2:c.4002T>G XP_006723790.1:p.Ser1334Arg
XM_006723728.2:c.3975T>G XP_006723791.1:p.Ser1325Arg
XM_006723730.2:c.3921T>G XP_006723793.1:p.Ser1307Arg
XM_006723732.2:c.3822T>G XP_006723795.1:p.Ser1274Arg
XM_006723733.1:c.3321T>G XP_006723796.1:p.Ser1107Arg
XM_011528647.1:c.4269T>G XP_011526949.1:p.Ser1423Arg
XM_011528648.1:c.4266T>G XP_011526950.1:p.Ser1422Arg
XM_011528649.1:c.4185T>G XP_011526951.1:p.Ser1395Arg
XM_011528650.1:c.4116T>G XP_011526952.1:p.Ser1372Arg
XM_011528651.1:c.3984T>G XP_011526953.1:p.Ser1328Arg
XM_011528652.1:c.3921T>G XP_011526954.1:p.Ser1307Arg
NM_001363734.1:c.3822T>G NP_001350663.1:p.Ser1274Arg
XM_006723727.3:c.4002T>G XP_006723790.1:p.Ser1334Arg
XM_006723728.3:c.3975T>G XP_006723791.1:p.Ser1325Arg
XM_006723730.4:c.3921T>G XP_006723793.1:p.Ser1307Arg
XM_011528648.3:c.4266T>G XP_011526950.1:p.Ser1422Arg
XM_011528652.2:c.3921T>G XP_011526954.1:p.Ser1307Arg
XM_017027704.1:c.3921T>G XP_016883193.1:p.Ser1307Arg
XM_017027705.1:c.3921T>G XP_016883194.1:p.Ser1307Arg
XM_017027706.1:c.3852T>G XP_016883195.1:p.Ser1284Arg
NM_015338.6:c.4005T>G MANE Select NP_056153.2:p.Ser1335Arg