Canonical Allele Identifier: CA1880009347

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868401T= , CM000671.2:g.127868401T=	GRCh38
NC_000009.11:g.130630680T= , CM000671.1:g.130630680T=	GRCh37
NC_000009.10:g.129670501T=	NCBI36
NG_011792.1:g.14343A=
NG_011792.2:g.14343A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.936A=
ENST00000643029.1:c.*2111A=	ENSP00000496586.1:n.*2111A=
ENST00000643338.1:c.*2000A=	ENSP00000495890.1:n.*2000A=
ENST00000644144.2:c.436A= MANE Select	ENSP00000494600.1:p.Ile146=
ENST00000645007.1:c.*2360A=	ENSP00000494773.1:n.*2360A=
ENST00000646171.1:c.*469A=	ENSP00000495484.1:n.*469A=
ENST00000223836.10:c.484A=	ENSP00000223836.10:p.Ile162=
ENST00000373156.5:c.436A=	ENSP00000362249.1:p.Ile146=
ENST00000373176.5:c.436A=	ENSP00000362271.1:p.Ile146=
ENST00000413016.5:c.258A=
ENST00000550143.5:c.216A=	ENSP00000449130.1:n.216A=
NM_000476.2:c.436A=	NP_000467.1:p.Ile146=
XM_005251786.2:c.484A=	XP_005251843.1:p.Ile162=
XM_011518348.1:c.436A=	XP_011516650.1:p.Ile146=
XM_011518349.1:c.256A=	XP_011516651.1:p.Ile86=
NM_001318121.1:c.436A=	NP_001305050.1:p.Ile146=
NM_001318122.1:c.484A=	NP_001305051.1:p.Ile162=
XM_017014428.1:c.436A=	XP_016869917.1:p.Ile146=
XM_024447439.1:c.415A=	XP_024303207.1:p.Ile139=
XM_024447440.1:c.256A=	XP_024303208.1:p.Ile86=
NM_001318122.2:c.484A=	NP_001305051.1:p.Ile162=
NM_000476.3:c.436A= MANE Select	NP_000467.1:p.Ile146=
NR_174625.1:n.3755A=
NR_174626.1:n.3598A=
NR_174627.1:n.3635A=
NR_174628.1:n.3013A=
NR_174629.1:n.2958A=
NR_174630.1:n.2994A=
NR_174631.1:n.2939A=
NR_174632.1:n.3028A=