Canonical Allele Identifier: CA1880009342

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868392G= , CM000671.2:g.127868392G=	GRCh38
NC_000009.11:g.130630671G= , CM000671.1:g.130630671G=	GRCh37
NC_000009.10:g.129670492G=	NCBI36
NG_011792.1:g.14352C=
NG_011792.2:g.14352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.945C=
ENST00000643029.1:c.*2120C=	ENSP00000496586.1:n.*2120C=
ENST00000643338.1:c.*2009C=	ENSP00000495890.1:n.*2009C=
ENST00000644144.2:c.445C= MANE Select	ENSP00000494600.1:p.Arg149=
ENST00000645007.1:c.*2369C=	ENSP00000494773.1:n.*2369C=
ENST00000646171.1:c.*478C=	ENSP00000495484.1:n.*478C=
ENST00000223836.10:c.493C=	ENSP00000223836.10:p.Arg165=
ENST00000373156.5:c.445C=	ENSP00000362249.1:p.Arg149=
ENST00000373176.5:c.445C=	ENSP00000362271.1:p.Arg149=
ENST00000413016.5:c.267C=
ENST00000550143.5:c.225C=	ENSP00000449130.1:n.225C=
NM_000476.2:c.445C=	NP_000467.1:p.Arg149=
XM_005251786.2:c.493C=	XP_005251843.1:p.Arg165=
XM_011518348.1:c.445C=	XP_011516650.1:p.Arg149=
XM_011518349.1:c.265C=	XP_011516651.1:p.Arg89=
NM_001318121.1:c.445C=	NP_001305050.1:p.Arg149=
NM_001318122.1:c.493C=	NP_001305051.1:p.Arg165=
XM_017014428.1:c.445C=	XP_016869917.1:p.Arg149=
XM_024447439.1:c.424C=	XP_024303207.1:p.Arg142=
XM_024447440.1:c.265C=	XP_024303208.1:p.Arg89=
NM_001318122.2:c.493C=	NP_001305051.1:p.Arg165=
NM_000476.3:c.445C= MANE Select	NP_000467.1:p.Arg149=
NR_174625.1:n.3764C=
NR_174626.1:n.3607C=
NR_174627.1:n.3644C=
NR_174628.1:n.3022C=
NR_174629.1:n.2967C=
NR_174630.1:n.3003C=
NR_174631.1:n.2948C=
NR_174632.1:n.3037C=