Canonical Allele Identifier: CA1880009365

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868440C= , CM000671.2:g.127868440C=	GRCh38
NC_000009.11:g.130630719C= , CM000671.1:g.130630719C=	GRCh37
NC_000009.10:g.129670540C=	NCBI36
NG_011792.1:g.14304G=
NG_011792.2:g.14304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.897G=
ENST00000643029.1:c.*2072G=	ENSP00000496586.1:n.*2072G=
ENST00000643338.1:c.*1961G=	ENSP00000495890.1:n.*1961G=
ENST00000644144.2:c.397G= MANE Select	ENSP00000494600.1:p.Gly133=
ENST00000645007.1:c.*2321G=	ENSP00000494773.1:n.*2321G=
ENST00000646171.1:c.*430G=	ENSP00000495484.1:n.*430G=
ENST00000223836.10:c.445G=	ENSP00000223836.10:p.Gly149=
ENST00000373156.5:c.397G=	ENSP00000362249.1:p.Gly133=
ENST00000373176.5:c.397G=	ENSP00000362271.1:p.Gly133=
ENST00000413016.5:c.219G=
ENST00000550143.5:c.177G=	ENSP00000449130.1:n.177G=
NM_000476.2:c.397G=	NP_000467.1:p.Gly133=
XM_005251786.2:c.445G=	XP_005251843.1:p.Gly149=
XM_011518348.1:c.397G=	XP_011516650.1:p.Gly133=
XM_011518349.1:c.217G=	XP_011516651.1:p.Gly73=
NM_001318121.1:c.397G=	NP_001305050.1:p.Gly133=
NM_001318122.1:c.445G=	NP_001305051.1:p.Gly149=
XM_017014428.1:c.397G=	XP_016869917.1:p.Gly133=
XM_024447439.1:c.376G=	XP_024303207.1:p.Gly126=
XM_024447440.1:c.217G=	XP_024303208.1:p.Gly73=
NM_001318122.2:c.445G=	NP_001305051.1:p.Gly149=
NM_000476.3:c.397G= MANE Select	NP_000467.1:p.Gly133=
NR_174625.1:n.3716G=
NR_174626.1:n.3559G=
NR_174627.1:n.3596G=
NR_174628.1:n.2974G=
NR_174629.1:n.2919G=
NR_174630.1:n.2955G=
NR_174631.1:n.2900G=
NR_174632.1:n.2989G=