Canonical Allele Identifier: CA1880009328

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868355A= , CM000671.2:g.127868355A=	GRCh38
NC_000009.11:g.130630634A= , CM000671.1:g.130630634A=	GRCh37
NC_000009.10:g.129670455A=	NCBI36
NG_011792.1:g.14389T=
NG_011792.2:g.14389T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.982T=
ENST00000643029.1:c.*2157T=	ENSP00000496586.1:n.*2157T=
ENST00000643338.1:c.*2046T=	ENSP00000495890.1:n.*2046T=
ENST00000644144.2:c.482T= MANE Select	ENSP00000494600.1:p.Ile161=
ENST00000645007.1:c.*2406T=	ENSP00000494773.1:n.*2406T=
ENST00000646171.1:c.*515T=	ENSP00000495484.1:n.*515T=
ENST00000223836.10:c.530T=	ENSP00000223836.10:p.Ile177=
ENST00000373156.5:c.482T=	ENSP00000362249.1:p.Ile161=
ENST00000373176.5:c.482T=	ENSP00000362271.1:p.Ile161=
ENST00000413016.5:c.304T=
ENST00000550143.5:c.262T=	ENSP00000449130.1:n.262T=
NM_000476.2:c.482T=	NP_000467.1:p.Ile161=
XM_005251786.2:c.530T=	XP_005251843.1:p.Ile177=
XM_011518348.1:c.482T=	XP_011516650.1:p.Ile161=
XM_011518349.1:c.302T=	XP_011516651.1:p.Ile101=
NM_001318121.1:c.482T=	NP_001305050.1:p.Ile161=
NM_001318122.1:c.530T=	NP_001305051.1:p.Ile177=
XM_017014428.1:c.482T=	XP_016869917.1:p.Ile161=
XM_024447439.1:c.461T=	XP_024303207.1:p.Ile154=
XM_024447440.1:c.302T=	XP_024303208.1:p.Ile101=
NM_001318122.2:c.530T=	NP_001305051.1:p.Ile177=
NM_000476.3:c.482T= MANE Select	NP_000467.1:p.Ile161=
NR_174625.1:n.3801T=
NR_174626.1:n.3644T=
NR_174627.1:n.3681T=
NR_174628.1:n.3059T=
NR_174629.1:n.3004T=
NR_174630.1:n.3040T=
NR_174631.1:n.2985T=
NR_174632.1:n.3074T=