Canonical Allele Identifier: CA1880009390

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868480G= , CM000671.2:g.127868480G=	GRCh38
NC_000009.11:g.130630759G= , CM000671.1:g.130630759G=	GRCh37
NC_000009.10:g.129670580G=	NCBI36
NG_011792.1:g.14264C=
NG_011792.2:g.14264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.857C=
ENST00000643029.1:c.*2032C=	ENSP00000496586.1:n.*2032C=
ENST00000643338.1:c.*1921C=	ENSP00000495890.1:n.*1921C=
ENST00000644144.2:c.357C= MANE Select	ENSP00000494600.1:p.Asp119=
ENST00000645007.1:c.*2281C=	ENSP00000494773.1:n.*2281C=
ENST00000646171.1:c.*390C=	ENSP00000495484.1:n.*390C=
ENST00000223836.10:c.405C=	ENSP00000223836.10:p.Asp135=
ENST00000373156.5:c.357C=	ENSP00000362249.1:p.Asp119=
ENST00000373176.5:c.357C=	ENSP00000362271.1:p.Asp119=
ENST00000413016.5:c.179C=
ENST00000550143.5:c.142-5C=	ENSP00000449130.1:n.142-5C=
ENST00000550992.1:c.*377C=	ENSP00000448741.1:n.*377C=
NM_000476.2:c.357C=	NP_000467.1:p.Asp119=
XM_005251786.2:c.405C=	XP_005251843.1:p.Asp135=
XM_011518348.1:c.357C=	XP_011516650.1:p.Asp119=
XM_011518349.1:c.177C=	XP_011516651.1:p.Asp59=
NM_001318121.1:c.357C=	NP_001305050.1:p.Asp119=
NM_001318122.1:c.405C=	NP_001305051.1:p.Asp135=
XM_017014428.1:c.357C=	XP_016869917.1:p.Asp119=
XM_024447439.1:c.336C=	XP_024303207.1:p.Asp112=
XM_024447440.1:c.177C=	XP_024303208.1:p.Asp59=
NM_001318122.2:c.405C=	NP_001305051.1:p.Asp135=
NM_000476.3:c.357C= MANE Select	NP_000467.1:p.Asp119=
NR_174625.1:n.3676C=
NR_174626.1:n.3524-5C=
NR_174627.1:n.3556C=
NR_174628.1:n.2934C=
NR_174629.1:n.2879C=
NR_174630.1:n.2915C=
NR_174631.1:n.2860C=
NR_174632.1:n.2949C=