Canonical Allele Identifier: CA408562614
Gene: ASXL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.32435938A>G , CM000682.2:g.32435938A>G GRCh38
NC_000020.10:g.31023741A>G , CM000682.1:g.31023741A>G GRCh37
NC_000020.9:g.30487402A>G NCBI36
NG_027868.1:g.82595A>G , LRG_630:g.82595A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375687.10:c.3226A>G MANE Select ENSP00000364839.4:p.Ile1076Val
ENST00000646985.1:c.3043A>G ENSP00000495053.1:p.Ile1015Val
ENST00000647223.1:n.5579A>G
ENST00000651418.1:c.1869+1357A>G ENSP00000499150.1:n.1869+1357A>G
ENST00000306058.9:c.3211A>G ENSP00000305119.5:p.Ile1071Val
ENST00000375687.8:c.3226A>G ENSP00000364839.4:p.Ile1076Val
ENST00000613218.4:c.3226A>G ENSP00000480487.1:p.Ile1076Val
ENST00000620121.4:c.3226A>G ENSP00000481978.1:p.Ile1076Val
NM_015338.5:c.3226A>G , LRG_630t1:c.3226A>G NP_056153.2:p.Ile1076Val
XM_006723727.2:c.3223A>G XP_006723790.1:p.Ile1075Val
XM_006723728.2:c.3196A>G XP_006723791.1:p.Ile1066Val
XM_006723730.2:c.3142A>G XP_006723793.1:p.Ile1048Val
XM_006723732.2:c.3043A>G XP_006723795.1:p.Ile1015Val
XM_006723733.1:c.2542A>G XP_006723796.1:p.Ile848Val
XM_011528647.1:c.3490A>G XP_011526949.1:p.Ile1164Val
XM_011528648.1:c.3487A>G XP_011526950.1:p.Ile1163Val
XM_011528649.1:c.3406A>G XP_011526951.1:p.Ile1136Val
XM_011528650.1:c.3337A>G XP_011526952.1:p.Ile1113Val
XM_011528651.1:c.3205A>G XP_011526953.1:p.Ile1069Val
XM_011528652.1:c.3142A>G XP_011526954.1:p.Ile1048Val
NM_001363734.1:c.3043A>G NP_001350663.1:p.Ile1015Val
XM_006723727.3:c.3223A>G XP_006723790.1:p.Ile1075Val
XM_006723728.3:c.3196A>G XP_006723791.1:p.Ile1066Val
XM_006723730.4:c.3142A>G XP_006723793.1:p.Ile1048Val
XM_011528648.3:c.3487A>G XP_011526950.1:p.Ile1163Val
XM_011528652.2:c.3142A>G XP_011526954.1:p.Ile1048Val
XM_017027704.1:c.3142A>G XP_016883193.1:p.Ile1048Val
XM_017027705.1:c.3142A>G XP_016883194.1:p.Ile1048Val
XM_017027706.1:c.3073A>G XP_016883195.1:p.Ile1025Val
NM_015338.6:c.3226A>G MANE Select NP_056153.2:p.Ile1076Val