Canonical Allele Identifier: CA374947277
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868410C>A , CM000671.2:g.127868410C>A GRCh38
NC_000009.11:g.130630689C>A , CM000671.1:g.130630689C>A GRCh37
NC_000009.10:g.129670510C>A NCBI36
NG_011792.1:g.14334G>T
NG_011792.2:g.14334G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.927G>T
ENST00000643029.1:c.*2102G>T ENSP00000496586.1:n.*2102G>T
ENST00000643338.1:c.*1991G>T ENSP00000495890.1:n.*1991G>T
ENST00000644144.2:c.427G>T MANE Select ENSP00000494600.1:p.Glu143Ter
ENST00000645007.1:c.*2351G>T ENSP00000494773.1:n.*2351G>T
ENST00000646171.1:c.*460G>T ENSP00000495484.1:n.*460G>T
ENST00000223836.10:c.475G>T ENSP00000223836.10:p.Glu159Ter
ENST00000373156.5:c.427G>T ENSP00000362249.1:p.Glu143Ter
ENST00000373176.5:c.427G>T ENSP00000362271.1:p.Glu143Ter
ENST00000413016.5:c.249G>T
ENST00000550143.5:c.207G>T ENSP00000449130.1:n.207G>T
NM_000476.2:c.427G>T NP_000467.1:p.Glu143Ter
XM_005251786.2:c.475G>T XP_005251843.1:p.Glu159Ter
XM_011518348.1:c.427G>T XP_011516650.1:p.Glu143Ter
XM_011518349.1:c.247G>T XP_011516651.1:p.Glu83Ter
NM_001318121.1:c.427G>T NP_001305050.1:p.Glu143Ter
NM_001318122.1:c.475G>T NP_001305051.1:p.Glu159Ter
XM_017014428.1:c.427G>T XP_016869917.1:p.Glu143Ter
XM_024447439.1:c.406G>T XP_024303207.1:p.Glu136Ter
XM_024447440.1:c.247G>T XP_024303208.1:p.Glu83Ter
NM_001318122.2:c.475G>T NP_001305051.1:p.Glu159Ter
NM_000476.3:c.427G>T MANE Select NP_000467.1:p.Glu143Ter
NR_174625.1:n.3746G>T
NR_174626.1:n.3589G>T
NR_174627.1:n.3626G>T
NR_174628.1:n.3004G>T
NR_174629.1:n.2949G>T
NR_174630.1:n.2985G>T
NR_174631.1:n.2930G>T
NR_174632.1:n.3019G>T