Canonical Allele Identifier: CA1880009338

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868381G= , CM000671.2:g.127868381G=	GRCh38
NC_000009.11:g.130630660G= , CM000671.1:g.130630660G=	GRCh37
NC_000009.10:g.129670481G=	NCBI36
NG_011792.1:g.14363C=
NG_011792.2:g.14363C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.956C=
ENST00000643029.1:c.*2131C=	ENSP00000496586.1:n.*2131C=
ENST00000643338.1:c.*2020C=	ENSP00000495890.1:n.*2020C=
ENST00000644144.2:c.456C= MANE Select	ENSP00000494600.1:p.Thr152=
ENST00000645007.1:c.*2380C=	ENSP00000494773.1:n.*2380C=
ENST00000646171.1:c.*489C=	ENSP00000495484.1:n.*489C=
ENST00000223836.10:c.504C=	ENSP00000223836.10:p.Thr168=
ENST00000373156.5:c.456C=	ENSP00000362249.1:p.Thr152=
ENST00000373176.5:c.456C=	ENSP00000362271.1:p.Thr152=
ENST00000413016.5:c.278C=
ENST00000550143.5:c.236C=	ENSP00000449130.1:n.236C=
NM_000476.2:c.456C=	NP_000467.1:p.Thr152=
XM_005251786.2:c.504C=	XP_005251843.1:p.Thr168=
XM_011518348.1:c.456C=	XP_011516650.1:p.Thr152=
XM_011518349.1:c.276C=	XP_011516651.1:p.Thr92=
NM_001318121.1:c.456C=	NP_001305050.1:p.Thr152=
NM_001318122.1:c.504C=	NP_001305051.1:p.Thr168=
XM_017014428.1:c.456C=	XP_016869917.1:p.Thr152=
XM_024447439.1:c.435C=	XP_024303207.1:p.Thr145=
XM_024447440.1:c.276C=	XP_024303208.1:p.Thr92=
NM_001318122.2:c.504C=	NP_001305051.1:p.Thr168=
NM_000476.3:c.456C= MANE Select	NP_000467.1:p.Thr152=
NR_174625.1:n.3775C=
NR_174626.1:n.3618C=
NR_174627.1:n.3655C=
NR_174628.1:n.3033C=
NR_174629.1:n.2978C=
NR_174630.1:n.3014C=
NR_174631.1:n.2959C=
NR_174632.1:n.3048C=