Canonical Allele Identifier: CA467224243
Gene: AK1 HGNC NCBI

Linked Data

dbSNP Id: rs1588612208
MyVariant Identifiers: chr9:g.130630723T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868444T>C , CM000671.2:g.127868444T>C GRCh38
NC_000009.11:g.130630723T>C , CM000671.1:g.130630723T>C GRCh37
NC_000009.10:g.129670544T>C NCBI36
NG_011792.1:g.14300A>G
NG_011792.2:g.14300A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.893A>G
ENST00000643029.1:c.*2068A>G ENSP00000496586.1:n.*2068A>G
ENST00000643338.1:c.*1957A>G ENSP00000495890.1:n.*1957A>G
ENST00000644144.2:c.393A>G MANE Select ENSP00000494600.1:p.Lys131=
ENST00000645007.1:c.*2317A>G ENSP00000494773.1:n.*2317A>G
ENST00000646171.1:c.*426A>G ENSP00000495484.1:n.*426A>G
ENST00000223836.10:c.441A>G ENSP00000223836.10:p.Lys147=
ENST00000373156.5:c.393A>G ENSP00000362249.1:p.Lys131=
ENST00000373176.5:c.393A>G ENSP00000362271.1:p.Lys131=
ENST00000413016.5:c.215A>G
ENST00000550143.5:c.173A>G ENSP00000449130.1:n.173A>G
NM_000476.2:c.393A>G NP_000467.1:p.Lys131=
XM_005251786.2:c.441A>G XP_005251843.1:p.Lys147=
XM_011518348.1:c.393A>G XP_011516650.1:p.Lys131=
XM_011518349.1:c.213A>G XP_011516651.1:p.Lys71=
NM_001318121.1:c.393A>G NP_001305050.1:p.Lys131=
NM_001318122.1:c.441A>G NP_001305051.1:p.Lys147=
XM_017014428.1:c.393A>G XP_016869917.1:p.Lys131=
XM_024447439.1:c.372A>G XP_024303207.1:p.Lys124=
XM_024447440.1:c.213A>G XP_024303208.1:p.Lys71=
NM_001318122.2:c.441A>G NP_001305051.1:p.Lys147=
NM_000476.3:c.393A>G MANE Select NP_000467.1:p.Lys131=
NR_174625.1:n.3712A>G
NR_174626.1:n.3555A>G
NR_174627.1:n.3592A>G
NR_174628.1:n.2970A>G
NR_174629.1:n.2915A>G
NR_174630.1:n.2951A>G
NR_174631.1:n.2896A>G
NR_174632.1:n.2985A>G