Canonical Allele Identifier: CA374946980
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868365C>G , CM000671.2:g.127868365C>G GRCh38
NC_000009.11:g.130630644C>G , CM000671.1:g.130630644C>G GRCh37
NC_000009.10:g.129670465C>G NCBI36
NG_011792.1:g.14379G>C
NG_011792.2:g.14379G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000476274.7:n.972G>C
ENST00000643029.1:c.*2147G>C ENSP00000496586.1:n.*2147G>C
ENST00000643338.1:c.*2036G>C ENSP00000495890.1:n.*2036G>C
ENST00000644144.2:c.472G>C MANE Select ENSP00000494600.1:p.Glu158Gln
ENST00000645007.1:c.*2396G>C ENSP00000494773.1:n.*2396G>C
ENST00000646171.1:c.*505G>C ENSP00000495484.1:n.*505G>C
ENST00000223836.10:c.520G>C ENSP00000223836.10:p.Glu174Gln
ENST00000373156.5:c.472G>C ENSP00000362249.1:p.Glu158Gln
ENST00000373176.5:c.472G>C ENSP00000362271.1:p.Glu158Gln
ENST00000413016.5:c.294G>C
ENST00000550143.5:c.252G>C ENSP00000449130.1:n.252G>C
NM_000476.2:c.472G>C NP_000467.1:p.Glu158Gln
XM_005251786.2:c.520G>C XP_005251843.1:p.Glu174Gln
XM_011518348.1:c.472G>C XP_011516650.1:p.Glu158Gln
XM_011518349.1:c.292G>C XP_011516651.1:p.Glu98Gln
NM_001318121.1:c.472G>C NP_001305050.1:p.Glu158Gln
NM_001318122.1:c.520G>C NP_001305051.1:p.Glu174Gln
XM_017014428.1:c.472G>C XP_016869917.1:p.Glu158Gln
XM_024447439.1:c.451G>C XP_024303207.1:p.Glu151Gln
XM_024447440.1:c.292G>C XP_024303208.1:p.Glu98Gln
NM_001318122.2:c.520G>C NP_001305051.1:p.Glu174Gln
NM_000476.3:c.472G>C MANE Select NP_000467.1:p.Glu158Gln
NR_174625.1:n.3791G>C
NR_174626.1:n.3634G>C
NR_174627.1:n.3671G>C
NR_174628.1:n.3049G>C
NR_174629.1:n.2994G>C
NR_174630.1:n.3030G>C
NR_174631.1:n.2975G>C
NR_174632.1:n.3064G>C