Canonical Allele Identifier: CA2838814299
Gene: AK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868455del , CM000671.2:g.127868455del GRCh38
NC_000009.11:g.130630734del , CM000671.1:g.130630734del GRCh37
NC_000009.10:g.129670555del NCBI36
NG_011792.1:g.14289del
NG_011792.2:g.14289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.882del
ENST00000643029.1:c.*2057del ENSP00000496586.1:n.*2057del
ENST00000643338.1:c.*1946del ENSP00000495890.1:n.*1946del
ENST00000644144.2:c.382del MANE Select ENSP00000494600.1:p.Arg128GlyfsTer3
ENST00000645007.1:c.*2306del ENSP00000494773.1:n.*2306del
ENST00000646171.1:c.*415del ENSP00000495484.1:n.*415del
ENST00000223836.10:c.430del ENSP00000223836.10:p.Arg144GlyfsTer3
ENST00000373156.5:c.382del ENSP00000362249.1:p.Arg128GlyfsTer3
ENST00000373176.5:c.382del ENSP00000362271.1:p.Arg128GlyfsTer3
ENST00000413016.5:c.204del
ENST00000550143.5:c.162del ENSP00000449130.1:n.162del
NM_000476.2:c.382del NP_000467.1:p.Arg128GlyfsTer3
XM_005251786.2:c.430del XP_005251843.1:p.Arg144GlyfsTer3
XM_011518348.1:c.382del XP_011516650.1:p.Arg128GlyfsTer3
XM_011518349.1:c.202del XP_011516651.1:p.Arg68GlyfsTer3
NM_001318121.1:c.382del NP_001305050.1:p.Arg128GlyfsTer3
NM_001318122.1:c.430del NP_001305051.1:p.Arg144GlyfsTer3
XM_017014428.1:c.382del XP_016869917.1:p.Arg128GlyfsTer3
XM_024447439.1:c.361del XP_024303207.1:p.Arg121GlyfsTer3
XM_024447440.1:c.202del XP_024303208.1:p.Arg68GlyfsTer3
NM_001318122.2:c.430del NP_001305051.1:p.Arg144GlyfsTer3
NM_000476.3:c.382del MANE Select NP_000467.1:p.Arg128GlyfsTer3
NR_174625.1:n.3701del
NR_174626.1:n.3544del
NR_174627.1:n.3581del
NR_174628.1:n.2959del
NR_174629.1:n.2904del
NR_174630.1:n.2940del
NR_174631.1:n.2885del
NR_174632.1:n.2974del