Canonical Allele Identifier: CA1880009346

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868397T= , CM000671.2:g.127868397T=	GRCh38
NC_000009.11:g.130630676T= , CM000671.1:g.130630676T=	GRCh37
NC_000009.10:g.129670497T=	NCBI36
NG_011792.1:g.14347A=
NG_011792.2:g.14347A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.940A=
ENST00000643029.1:c.*2115A=	ENSP00000496586.1:n.*2115A=
ENST00000643338.1:c.*2004A=	ENSP00000495890.1:n.*2004A=
ENST00000644144.2:c.440A= MANE Select	ENSP00000494600.1:p.Lys147=
ENST00000645007.1:c.*2364A=	ENSP00000494773.1:n.*2364A=
ENST00000646171.1:c.*473A=	ENSP00000495484.1:n.*473A=
ENST00000223836.10:c.488A=	ENSP00000223836.10:p.Lys163=
ENST00000373156.5:c.440A=	ENSP00000362249.1:p.Lys147=
ENST00000373176.5:c.440A=	ENSP00000362271.1:p.Lys147=
ENST00000413016.5:c.262A=
ENST00000550143.5:c.220A=	ENSP00000449130.1:n.220A=
NM_000476.2:c.440A=	NP_000467.1:p.Lys147=
XM_005251786.2:c.488A=	XP_005251843.1:p.Lys163=
XM_011518348.1:c.440A=	XP_011516650.1:p.Lys147=
XM_011518349.1:c.260A=	XP_011516651.1:p.Lys87=
NM_001318121.1:c.440A=	NP_001305050.1:p.Lys147=
NM_001318122.1:c.488A=	NP_001305051.1:p.Lys163=
XM_017014428.1:c.440A=	XP_016869917.1:p.Lys147=
XM_024447439.1:c.419A=	XP_024303207.1:p.Lys140=
XM_024447440.1:c.260A=	XP_024303208.1:p.Lys87=
NM_001318122.2:c.488A=	NP_001305051.1:p.Lys163=
NM_000476.3:c.440A= MANE Select	NP_000467.1:p.Lys147=
NR_174625.1:n.3759A=
NR_174626.1:n.3602A=
NR_174627.1:n.3639A=
NR_174628.1:n.3017A=
NR_174629.1:n.2962A=
NR_174630.1:n.2998A=
NR_174631.1:n.2943A=
NR_174632.1:n.3032A=