Canonical Allele Identifier: CA374947724

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630763A>G (hg19) ; chr9:g.127868484A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868484A>G , CM000671.2:g.127868484A>G	GRCh38
NC_000009.11:g.130630763A>G , CM000671.1:g.130630763A>G	GRCh37
NC_000009.10:g.129670584A>G	NCBI36
NG_011792.1:g.14260T>C
NG_011792.2:g.14260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.853T>C
ENST00000643029.1:c.*2028T>C	ENSP00000496586.1:n.*2028T>C
ENST00000643338.1:c.*1917T>C	ENSP00000495890.1:n.*1917T>C
ENST00000644144.2:c.353T>C MANE Select	ENSP00000494600.1:p.Val118Ala
ENST00000645007.1:c.*2277T>C	ENSP00000494773.1:n.*2277T>C
ENST00000646171.1:c.*386T>C	ENSP00000495484.1:n.*386T>C
ENST00000223836.10:c.401T>C	ENSP00000223836.10:p.Val134Ala
ENST00000373156.5:c.353T>C	ENSP00000362249.1:p.Val118Ala
ENST00000373176.5:c.353T>C	ENSP00000362271.1:p.Val118Ala
ENST00000413016.5:c.175T>C
ENST00000550143.5:c.142-9T>C	ENSP00000449130.1:n.142-9T>C
ENST00000550992.1:c.*373T>C	ENSP00000448741.1:n.*373T>C
NM_000476.2:c.353T>C	NP_000467.1:p.Val118Ala
XM_005251786.2:c.401T>C	XP_005251843.1:p.Val134Ala
XM_011518348.1:c.353T>C	XP_011516650.1:p.Val118Ala
XM_011518349.1:c.173T>C	XP_011516651.1:p.Val58Ala
NM_001318121.1:c.353T>C	NP_001305050.1:p.Val118Ala
NM_001318122.1:c.401T>C	NP_001305051.1:p.Val134Ala
XM_017014428.1:c.353T>C	XP_016869917.1:p.Val118Ala
XM_024447439.1:c.332T>C	XP_024303207.1:p.Val111Ala
XM_024447440.1:c.173T>C	XP_024303208.1:p.Val58Ala
NM_001318122.2:c.401T>C	NP_001305051.1:p.Val134Ala
NM_000476.3:c.353T>C MANE Select	NP_000467.1:p.Val118Ala
NR_174625.1:n.3672T>C
NR_174626.1:n.3524-9T>C
NR_174627.1:n.3552T>C
NR_174628.1:n.2930T>C
NR_174629.1:n.2875T>C
NR_174630.1:n.2911T>C
NR_174631.1:n.2856T>C
NR_174632.1:n.2945T>C