Canonical Allele Identifier: CA1880009341

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868391C= , CM000671.2:g.127868391C=	GRCh38
NC_000009.11:g.130630670C= , CM000671.1:g.130630670C=	GRCh37
NC_000009.10:g.129670491C=	NCBI36
NG_011792.1:g.14353G=
NG_011792.2:g.14353G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.946G=
ENST00000643029.1:c.*2121G=	ENSP00000496586.1:n.*2121G=
ENST00000643338.1:c.*2010G=	ENSP00000495890.1:n.*2010G=
ENST00000644144.2:c.446G= MANE Select	ENSP00000494600.1:p.Arg149=
ENST00000645007.1:c.*2370G=	ENSP00000494773.1:n.*2370G=
ENST00000646171.1:c.*479G=	ENSP00000495484.1:n.*479G=
ENST00000223836.10:c.494G=	ENSP00000223836.10:p.Arg165=
ENST00000373156.5:c.446G=	ENSP00000362249.1:p.Arg149=
ENST00000373176.5:c.446G=	ENSP00000362271.1:p.Arg149=
ENST00000413016.5:c.268G=
ENST00000550143.5:c.226G=	ENSP00000449130.1:n.226G=
NM_000476.2:c.446G=	NP_000467.1:p.Arg149=
XM_005251786.2:c.494G=	XP_005251843.1:p.Arg165=
XM_011518348.1:c.446G=	XP_011516650.1:p.Arg149=
XM_011518349.1:c.266G=	XP_011516651.1:p.Arg89=
NM_001318121.1:c.446G=	NP_001305050.1:p.Arg149=
NM_001318122.1:c.494G=	NP_001305051.1:p.Arg165=
XM_017014428.1:c.446G=	XP_016869917.1:p.Arg149=
XM_024447439.1:c.425G=	XP_024303207.1:p.Arg142=
XM_024447440.1:c.266G=	XP_024303208.1:p.Arg89=
NM_001318122.2:c.494G=	NP_001305051.1:p.Arg165=
NM_000476.3:c.446G= MANE Select	NP_000467.1:p.Arg149=
NR_174625.1:n.3765G=
NR_174626.1:n.3608G=
NR_174627.1:n.3645G=
NR_174628.1:n.3023G=
NR_174629.1:n.2968G=
NR_174630.1:n.3004G=
NR_174631.1:n.2949G=
NR_174632.1:n.3038G=