Canonical Allele Identifier: CA1880009359

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868428C= , CM000671.2:g.127868428C=	GRCh38
NC_000009.11:g.130630707C= , CM000671.1:g.130630707C=	GRCh37
NC_000009.10:g.129670528C=	NCBI36
NG_011792.1:g.14316G=
NG_011792.2:g.14316G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.909G=
ENST00000643029.1:c.*2084G=	ENSP00000496586.1:n.*2084G=
ENST00000643338.1:c.*1973G=	ENSP00000495890.1:n.*1973G=
ENST00000644144.2:c.409G= MANE Select	ENSP00000494600.1:p.Gly137=
ENST00000645007.1:c.*2333G=	ENSP00000494773.1:n.*2333G=
ENST00000646171.1:c.*442G=	ENSP00000495484.1:n.*442G=
ENST00000223836.10:c.457G=	ENSP00000223836.10:p.Gly153=
ENST00000373156.5:c.409G=	ENSP00000362249.1:p.Gly137=
ENST00000373176.5:c.409G=	ENSP00000362271.1:p.Gly137=
ENST00000413016.5:c.231G=
ENST00000550143.5:c.189G=	ENSP00000449130.1:n.189G=
NM_000476.2:c.409G=	NP_000467.1:p.Gly137=
XM_005251786.2:c.457G=	XP_005251843.1:p.Gly153=
XM_011518348.1:c.409G=	XP_011516650.1:p.Gly137=
XM_011518349.1:c.229G=	XP_011516651.1:p.Gly77=
NM_001318121.1:c.409G=	NP_001305050.1:p.Gly137=
NM_001318122.1:c.457G=	NP_001305051.1:p.Gly153=
XM_017014428.1:c.409G=	XP_016869917.1:p.Gly137=
XM_024447439.1:c.388G=	XP_024303207.1:p.Gly130=
XM_024447440.1:c.229G=	XP_024303208.1:p.Gly77=
NM_001318122.2:c.457G=	NP_001305051.1:p.Gly153=
NM_000476.3:c.409G= MANE Select	NP_000467.1:p.Gly137=
NR_174625.1:n.3728G=
NR_174626.1:n.3571G=
NR_174627.1:n.3608G=
NR_174628.1:n.2986G=
NR_174629.1:n.2931G=
NR_174630.1:n.2967G=
NR_174631.1:n.2912G=
NR_174632.1:n.3001G=