Canonical Allele Identifier: CA1880009369

Gene: AK1

Genomic Alleles

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

Transcript Alleles

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