Canonical Allele Identifier: CA1880009351

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868416C= , CM000671.2:g.127868416C=	GRCh38
NC_000009.11:g.130630695C= , CM000671.1:g.130630695C=	GRCh37
NC_000009.10:g.129670516C=	NCBI36
NG_011792.1:g.14328G=
NG_011792.2:g.14328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.921G=
ENST00000643029.1:c.*2096G=	ENSP00000496586.1:n.*2096G=
ENST00000643338.1:c.*1985G=	ENSP00000495890.1:n.*1985G=
ENST00000644144.2:c.421G= MANE Select	ENSP00000494600.1:p.Asp141=
ENST00000645007.1:c.*2345G=	ENSP00000494773.1:n.*2345G=
ENST00000646171.1:c.*454G=	ENSP00000495484.1:n.*454G=
ENST00000223836.10:c.469G=	ENSP00000223836.10:p.Asp157=
ENST00000373156.5:c.421G=	ENSP00000362249.1:p.Asp141=
ENST00000373176.5:c.421G=	ENSP00000362271.1:p.Asp141=
ENST00000413016.5:c.243G=
ENST00000550143.5:c.201G=	ENSP00000449130.1:n.201G=
NM_000476.2:c.421G=	NP_000467.1:p.Asp141=
XM_005251786.2:c.469G=	XP_005251843.1:p.Asp157=
XM_011518348.1:c.421G=	XP_011516650.1:p.Asp141=
XM_011518349.1:c.241G=	XP_011516651.1:p.Asp81=
NM_001318121.1:c.421G=	NP_001305050.1:p.Asp141=
NM_001318122.1:c.469G=	NP_001305051.1:p.Asp157=
XM_017014428.1:c.421G=	XP_016869917.1:p.Asp141=
XM_024447439.1:c.400G=	XP_024303207.1:p.Asp134=
XM_024447440.1:c.241G=	XP_024303208.1:p.Asp81=
NM_001318122.2:c.469G=	NP_001305051.1:p.Asp157=
NM_000476.3:c.421G= MANE Select	NP_000467.1:p.Asp141=
NR_174625.1:n.3740G=
NR_174626.1:n.3583G=
NR_174627.1:n.3620G=
NR_174628.1:n.2998G=
NR_174629.1:n.2943G=
NR_174630.1:n.2979G=
NR_174631.1:n.2924G=
NR_174632.1:n.3013G=