Canonical Allele Identifier: CA467224559
Gene: AK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.130630771C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868492C>G , CM000671.2:g.127868492C>G GRCh38
NC_000009.11:g.130630771C>G , CM000671.1:g.130630771C>G GRCh37
NC_000009.10:g.129670592C>G NCBI36
NG_011792.1:g.14252G>C
NG_011792.2:g.14252G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.845G>C
ENST00000643029.1:c.*2020G>C ENSP00000496586.1:n.*2020G>C
ENST00000643338.1:c.*1909G>C ENSP00000495890.1:n.*1909G>C
ENST00000644144.2:c.345G>C MANE Select ENSP00000494600.1:p.Leu115=
ENST00000645007.1:c.*2269G>C ENSP00000494773.1:n.*2269G>C
ENST00000646171.1:c.*378G>C ENSP00000495484.1:n.*378G>C
ENST00000223836.10:c.393G>C ENSP00000223836.10:p.Leu131=
ENST00000373156.5:c.345G>C ENSP00000362249.1:p.Leu115=
ENST00000373176.5:c.345G>C ENSP00000362271.1:p.Leu115=
ENST00000413016.5:c.167G>C
ENST00000550143.5:c.142-17G>C ENSP00000449130.1:n.142-17G>C
ENST00000550992.1:c.*365G>C ENSP00000448741.1:n.*365G>C
NM_000476.2:c.345G>C NP_000467.1:p.Leu115=
XM_005251786.2:c.393G>C XP_005251843.1:p.Leu131=
XM_011518348.1:c.345G>C XP_011516650.1:p.Leu115=
XM_011518349.1:c.165G>C XP_011516651.1:p.Leu55=
NM_001318121.1:c.345G>C NP_001305050.1:p.Leu115=
NM_001318122.1:c.393G>C NP_001305051.1:p.Leu131=
XM_017014428.1:c.345G>C XP_016869917.1:p.Leu115=
XM_024447439.1:c.324G>C XP_024303207.1:p.Leu108=
XM_024447440.1:c.165G>C XP_024303208.1:p.Leu55=
NM_001318122.2:c.393G>C NP_001305051.1:p.Leu131=
NM_000476.3:c.345G>C MANE Select NP_000467.1:p.Leu115=
NR_174625.1:n.3664G>C
NR_174626.1:n.3524-17G>C
NR_174627.1:n.3544G>C
NR_174628.1:n.2922G>C
NR_174629.1:n.2867G>C
NR_174630.1:n.2903G>C
NR_174631.1:n.2848G>C
NR_174632.1:n.2937G>C