Canonical Allele Identifier: CA374947073
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868376T>A , CM000671.2:g.127868376T>A GRCh38
NC_000009.11:g.130630655T>A , CM000671.1:g.130630655T>A GRCh37
NC_000009.10:g.129670476T>A NCBI36
NG_011792.1:g.14368A>T
NG_011792.2:g.14368A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.961A>T
ENST00000643029.1:c.*2136A>T ENSP00000496586.1:n.*2136A>T
ENST00000643338.1:c.*2025A>T ENSP00000495890.1:n.*2025A>T
ENST00000644144.2:c.461A>T MANE Select ENSP00000494600.1:p.Tyr154Phe
ENST00000645007.1:c.*2385A>T ENSP00000494773.1:n.*2385A>T
ENST00000646171.1:c.*494A>T ENSP00000495484.1:n.*494A>T
ENST00000223836.10:c.509A>T ENSP00000223836.10:p.Tyr170Phe
ENST00000373156.5:c.461A>T ENSP00000362249.1:p.Tyr154Phe
ENST00000373176.5:c.461A>T ENSP00000362271.1:p.Tyr154Phe
ENST00000413016.5:c.283A>T
ENST00000550143.5:c.241A>T ENSP00000449130.1:n.241A>T
NM_000476.2:c.461A>T NP_000467.1:p.Tyr154Phe
XM_005251786.2:c.509A>T XP_005251843.1:p.Tyr170Phe
XM_011518348.1:c.461A>T XP_011516650.1:p.Tyr154Phe
XM_011518349.1:c.281A>T XP_011516651.1:p.Tyr94Phe
NM_001318121.1:c.461A>T NP_001305050.1:p.Tyr154Phe
NM_001318122.1:c.509A>T NP_001305051.1:p.Tyr170Phe
XM_017014428.1:c.461A>T XP_016869917.1:p.Tyr154Phe
XM_024447439.1:c.440A>T XP_024303207.1:p.Tyr147Phe
XM_024447440.1:c.281A>T XP_024303208.1:p.Tyr94Phe
NM_001318122.2:c.509A>T NP_001305051.1:p.Tyr170Phe
NM_000476.3:c.461A>T MANE Select NP_000467.1:p.Tyr154Phe
NR_174625.1:n.3780A>T
NR_174626.1:n.3623A>T
NR_174627.1:n.3660A>T
NR_174628.1:n.3038A>T
NR_174629.1:n.2983A>T
NR_174630.1:n.3019A>T
NR_174631.1:n.2964A>T
NR_174632.1:n.3053A>T