Canonical Allele Identifier: CA1880009386

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868470C= , CM000671.2:g.127868470C=	GRCh38
NC_000009.11:g.130630749C= , CM000671.1:g.130630749C=	GRCh37
NC_000009.10:g.129670570C=	NCBI36
NG_011792.1:g.14274G=
NG_011792.2:g.14274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.867G=
ENST00000643029.1:c.*2042G=	ENSP00000496586.1:n.*2042G=
ENST00000643338.1:c.*1931G=	ENSP00000495890.1:n.*1931G=
ENST00000644144.2:c.367G= MANE Select	ENSP00000494600.1:p.Glu123=
ENST00000645007.1:c.*2291G=	ENSP00000494773.1:n.*2291G=
ENST00000646171.1:c.*400G=	ENSP00000495484.1:n.*400G=
ENST00000223836.10:c.415G=	ENSP00000223836.10:p.Glu139=
ENST00000373156.5:c.367G=	ENSP00000362249.1:p.Glu123=
ENST00000373176.5:c.367G=	ENSP00000362271.1:p.Glu123=
ENST00000413016.5:c.189G=
ENST00000550143.5:c.147G=	ENSP00000449130.1:p.Leu49=
ENST00000550992.1:c.*387G=	ENSP00000448741.1:n.*387G=
NM_000476.2:c.367G=	NP_000467.1:p.Glu123=
XM_005251786.2:c.415G=	XP_005251843.1:p.Glu139=
XM_011518348.1:c.367G=	XP_011516650.1:p.Glu123=
XM_011518349.1:c.187G=	XP_011516651.1:p.Glu63=
NM_001318121.1:c.367G=	NP_001305050.1:p.Glu123=
NM_001318122.1:c.415G=	NP_001305051.1:p.Glu139=
XM_017014428.1:c.367G=	XP_016869917.1:p.Glu123=
XM_024447439.1:c.346G=	XP_024303207.1:p.Glu116=
XM_024447440.1:c.187G=	XP_024303208.1:p.Glu63=
NM_001318122.2:c.415G=	NP_001305051.1:p.Glu139=
NM_000476.3:c.367G= MANE Select	NP_000467.1:p.Glu123=
NR_174625.1:n.3686G=
NR_174626.1:n.3529G=
NR_174627.1:n.3566G=
NR_174628.1:n.2944G=
NR_174629.1:n.2889G=
NR_174630.1:n.2925G=
NR_174631.1:n.2870G=
NR_174632.1:n.2959G=