Canonical Allele Identifier: CA374947046
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868373T>G , CM000671.2:g.127868373T>G GRCh38
NC_000009.11:g.130630652T>G , CM000671.1:g.130630652T>G GRCh37
NC_000009.10:g.129670473T>G NCBI36
NG_011792.1:g.14371A>C
NG_011792.2:g.14371A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.964A>C
ENST00000643029.1:c.*2139A>C ENSP00000496586.1:n.*2139A>C
ENST00000643338.1:c.*2028A>C ENSP00000495890.1:n.*2028A>C
ENST00000644144.2:c.464A>C MANE Select ENSP00000494600.1:p.Lys155Thr
ENST00000645007.1:c.*2388A>C ENSP00000494773.1:n.*2388A>C
ENST00000646171.1:c.*497A>C ENSP00000495484.1:n.*497A>C
ENST00000223836.10:c.512A>C ENSP00000223836.10:p.Lys171Thr
ENST00000373156.5:c.464A>C ENSP00000362249.1:p.Lys155Thr
ENST00000373176.5:c.464A>C ENSP00000362271.1:p.Lys155Thr
ENST00000413016.5:c.286A>C
ENST00000550143.5:c.244A>C ENSP00000449130.1:n.244A>C
NM_000476.2:c.464A>C NP_000467.1:p.Lys155Thr
XM_005251786.2:c.512A>C XP_005251843.1:p.Lys171Thr
XM_011518348.1:c.464A>C XP_011516650.1:p.Lys155Thr
XM_011518349.1:c.284A>C XP_011516651.1:p.Lys95Thr
NM_001318121.1:c.464A>C NP_001305050.1:p.Lys155Thr
NM_001318122.1:c.512A>C NP_001305051.1:p.Lys171Thr
XM_017014428.1:c.464A>C XP_016869917.1:p.Lys155Thr
XM_024447439.1:c.443A>C XP_024303207.1:p.Lys148Thr
XM_024447440.1:c.284A>C XP_024303208.1:p.Lys95Thr
NM_001318122.2:c.512A>C NP_001305051.1:p.Lys171Thr
NM_000476.3:c.464A>C MANE Select NP_000467.1:p.Lys155Thr
NR_174625.1:n.3783A>C
NR_174626.1:n.3626A>C
NR_174627.1:n.3663A>C
NR_174628.1:n.3041A>C
NR_174629.1:n.2986A>C
NR_174630.1:n.3022A>C
NR_174631.1:n.2967A>C
NR_174632.1:n.3056A>C