Canonical Allele Identifier: CA408561771
Gene: ASXL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32435701G>T , CM000682.2:g.32435701G>T GRCh38
NC_000020.10:g.31023504G>T , CM000682.1:g.31023504G>T GRCh37
NC_000020.9:g.30487165G>T NCBI36
NG_027868.1:g.82358G>T , LRG_630:g.82358G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.2989G>T MANE Select ENSP00000364839.4:p.Glu997Ter
ENST00000646985.1:c.2806G>T ENSP00000495053.1:p.Glu936Ter
ENST00000647223.1:n.5342G>T
ENST00000651418.1:c.1869+1120G>T ENSP00000499150.1:n.1869+1120G>T
ENST00000306058.9:c.2974G>T ENSP00000305119.5:p.Glu992Ter
ENST00000375687.8:c.2989G>T ENSP00000364839.4:p.Glu997Ter
ENST00000613218.4:c.2989G>T ENSP00000480487.1:p.Glu997Ter
ENST00000620121.4:c.2989G>T ENSP00000481978.1:p.Glu997Ter
NM_015338.5:c.2989G>T , LRG_630t1:c.2989G>T NP_056153.2:p.Glu997Ter
XM_006723727.2:c.2986G>T XP_006723790.1:p.Glu996Ter
XM_006723728.2:c.2959G>T XP_006723791.1:p.Glu987Ter
XM_006723730.2:c.2905G>T XP_006723793.1:p.Glu969Ter
XM_006723732.2:c.2806G>T XP_006723795.1:p.Glu936Ter
XM_006723733.1:c.2305G>T XP_006723796.1:p.Glu769Ter
XM_011528647.1:c.3253G>T XP_011526949.1:p.Glu1085Ter
XM_011528648.1:c.3250G>T XP_011526950.1:p.Glu1084Ter
XM_011528649.1:c.3169G>T XP_011526951.1:p.Glu1057Ter
XM_011528650.1:c.3100G>T XP_011526952.1:p.Glu1034Ter
XM_011528651.1:c.2968G>T XP_011526953.1:p.Glu990Ter
XM_011528652.1:c.2905G>T XP_011526954.1:p.Glu969Ter
NM_001363734.1:c.2806G>T NP_001350663.1:p.Glu936Ter
XM_006723727.3:c.2986G>T XP_006723790.1:p.Glu996Ter
XM_006723728.3:c.2959G>T XP_006723791.1:p.Glu987Ter
XM_006723730.4:c.2905G>T XP_006723793.1:p.Glu969Ter
XM_011528648.3:c.3250G>T XP_011526950.1:p.Glu1084Ter
XM_011528652.2:c.2905G>T XP_011526954.1:p.Glu969Ter
XM_017027704.1:c.2905G>T XP_016883193.1:p.Glu969Ter
XM_017027705.1:c.2905G>T XP_016883194.1:p.Glu969Ter
XM_017027706.1:c.2836G>T XP_016883195.1:p.Glu946Ter
NM_015338.6:c.2989G>T MANE Select NP_056153.2:p.Glu997Ter
Search 100 bp 5'
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