Canonical Allele Identifier: CA374946987
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868367G>T , CM000671.2:g.127868367G>T GRCh38
NC_000009.11:g.130630646G>T , CM000671.1:g.130630646G>T GRCh37
NC_000009.10:g.129670467G>T NCBI36
NG_011792.1:g.14377C>A
NG_011792.2:g.14377C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000476274.7:n.970C>A
ENST00000643029.1:c.*2145C>A ENSP00000496586.1:n.*2145C>A
ENST00000643338.1:c.*2034C>A ENSP00000495890.1:n.*2034C>A
ENST00000644144.2:c.470C>A MANE Select ENSP00000494600.1:p.Thr157Lys
ENST00000645007.1:c.*2394C>A ENSP00000494773.1:n.*2394C>A
ENST00000646171.1:c.*503C>A ENSP00000495484.1:n.*503C>A
ENST00000223836.10:c.518C>A ENSP00000223836.10:p.Thr173Lys
ENST00000373156.5:c.470C>A ENSP00000362249.1:p.Thr157Lys
ENST00000373176.5:c.470C>A ENSP00000362271.1:p.Thr157Lys
ENST00000413016.5:c.292C>A
ENST00000550143.5:c.250C>A ENSP00000449130.1:n.250C>A
NM_000476.2:c.470C>A NP_000467.1:p.Thr157Lys
XM_005251786.2:c.518C>A XP_005251843.1:p.Thr173Lys
XM_011518348.1:c.470C>A XP_011516650.1:p.Thr157Lys
XM_011518349.1:c.290C>A XP_011516651.1:p.Thr97Lys
NM_001318121.1:c.470C>A NP_001305050.1:p.Thr157Lys
NM_001318122.1:c.518C>A NP_001305051.1:p.Thr173Lys
XM_017014428.1:c.470C>A XP_016869917.1:p.Thr157Lys
XM_024447439.1:c.449C>A XP_024303207.1:p.Thr150Lys
XM_024447440.1:c.290C>A XP_024303208.1:p.Thr97Lys
NM_001318122.2:c.518C>A NP_001305051.1:p.Thr173Lys
NM_000476.3:c.470C>A MANE Select NP_000467.1:p.Thr157Lys
NR_174625.1:n.3789C>A
NR_174626.1:n.3632C>A
NR_174627.1:n.3669C>A
NR_174628.1:n.3047C>A
NR_174629.1:n.2992C>A
NR_174630.1:n.3028C>A
NR_174631.1:n.2973C>A
NR_174632.1:n.3062C>A