Canonical Allele Identifier: CA1880009333
Gene: AK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868360A= , CM000671.2:g.127868360A= GRCh38
NC_000009.11:g.130630639A= , CM000671.1:g.130630639A= GRCh37
NC_000009.10:g.129670460A= NCBI36
NG_011792.2:g.14384T=

Transcript Alleles

HGVS Amino-acid change
ENST00000476274.7:n.977T=
ENST00000643029.1:c.*2152T= ENSP00000496586.1:n.*2152T=
ENST00000643338.1:c.*2041T= ENSP00000495890.1:n.*2041T=
ENST00000644144.2:c.477T= MANE Select ENSP00000494600.1:p.Pro159=
ENST00000645007.1:c.*2401T= ENSP00000494773.1:n.*2401T=
ENST00000646171.1:c.*510T= ENSP00000495484.1:n.*510T=
ENST00000223836.10:c.525T= ENSP00000223836.10:p.Pro175=
ENST00000373156.5:c.477T= ENSP00000362249.1:p.Pro159=
ENST00000373176.5:c.477T= ENSP00000362271.1:p.Pro159=
ENST00000413016.5:c.299T=
ENST00000550143.5:c.257T= ENSP00000449130.1:n.257T=
XM_005251786.2:c.525T= XP_005251843.1:p.Pro175=
XM_011518348.1:c.477T= XP_011516650.1:p.Pro159=
XM_011518349.1:c.297T= XP_011516651.1:p.Pro99=
XM_017014428.1:c.477T= XP_016869917.1:p.Pro159=
XM_024447439.1:c.456T= XP_024303207.1:p.Pro152=
XM_024447440.1:c.297T= XP_024303208.1:p.Pro99=
NM_001318122.2:c.525T= NP_001305051.1:p.Pro175=
NM_000476.3:c.477T= MANE Select NP_000467.1:p.Pro159=
NR_174625.1:n.3796T=
NR_174626.1:n.3639T=
NR_174627.1:n.3676T=
NR_174628.1:n.3054T=
NR_174629.1:n.2999T=
NR_174630.1:n.3035T=
NR_174631.1:n.2980T=
NR_174632.1:n.3069T=