Canonical Allele Identifier: CA1880009354

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868423A= , CM000671.2:g.127868423A=	GRCh38
NC_000009.11:g.130630702A= , CM000671.1:g.130630702A=	GRCh37
NC_000009.10:g.129670523A=	NCBI36
NG_011792.1:g.14321T=
NG_011792.2:g.14321T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.914T=
ENST00000643029.1:c.*2089T=	ENSP00000496586.1:n.*2089T=
ENST00000643338.1:c.*1978T=	ENSP00000495890.1:n.*1978T=
ENST00000644144.2:c.414T= MANE Select	ENSP00000494600.1:p.Arg138=
ENST00000645007.1:c.*2338T=	ENSP00000494773.1:n.*2338T=
ENST00000646171.1:c.*447T=	ENSP00000495484.1:n.*447T=
ENST00000223836.10:c.462T=	ENSP00000223836.10:p.Arg154=
ENST00000373156.5:c.414T=	ENSP00000362249.1:p.Arg138=
ENST00000373176.5:c.414T=	ENSP00000362271.1:p.Arg138=
ENST00000413016.5:c.236T=
ENST00000550143.5:c.194T=	ENSP00000449130.1:n.194T=
NM_000476.2:c.414T=	NP_000467.1:p.Arg138=
XM_005251786.2:c.462T=	XP_005251843.1:p.Arg154=
XM_011518348.1:c.414T=	XP_011516650.1:p.Arg138=
XM_011518349.1:c.234T=	XP_011516651.1:p.Arg78=
NM_001318121.1:c.414T=	NP_001305050.1:p.Arg138=
NM_001318122.1:c.462T=	NP_001305051.1:p.Arg154=
XM_017014428.1:c.414T=	XP_016869917.1:p.Arg138=
XM_024447439.1:c.393T=	XP_024303207.1:p.Arg131=
XM_024447440.1:c.234T=	XP_024303208.1:p.Arg78=
NM_001318122.2:c.462T=	NP_001305051.1:p.Arg154=
NM_000476.3:c.414T= MANE Select	NP_000467.1:p.Arg138=
NR_174625.1:n.3733T=
NR_174626.1:n.3576T=
NR_174627.1:n.3613T=
NR_174628.1:n.2991T=
NR_174629.1:n.2936T=
NR_174630.1:n.2972T=
NR_174631.1:n.2917T=
NR_174632.1:n.3006T=