Canonical Allele Identifier: CA467223511

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630651C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868372C>T , CM000671.2:g.127868372C>T	GRCh38
NC_000009.11:g.130630651C>T , CM000671.1:g.130630651C>T	GRCh37
NC_000009.10:g.129670472C>T	NCBI36
NG_011792.1:g.14372G>A
NG_011792.2:g.14372G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.965G>A
ENST00000643029.1:c.*2140G>A	ENSP00000496586.1:n.*2140G>A
ENST00000643338.1:c.*2029G>A	ENSP00000495890.1:n.*2029G>A
ENST00000644144.2:c.465G>A MANE Select	ENSP00000494600.1:p.Lys155=
ENST00000645007.1:c.*2389G>A	ENSP00000494773.1:n.*2389G>A
ENST00000646171.1:c.*498G>A	ENSP00000495484.1:n.*498G>A
ENST00000223836.10:c.513G>A	ENSP00000223836.10:p.Lys171=
ENST00000373156.5:c.465G>A	ENSP00000362249.1:p.Lys155=
ENST00000373176.5:c.465G>A	ENSP00000362271.1:p.Lys155=
ENST00000413016.5:c.287G>A
ENST00000550143.5:c.245G>A	ENSP00000449130.1:n.245G>A
NM_000476.2:c.465G>A	NP_000467.1:p.Lys155=
XM_005251786.2:c.513G>A	XP_005251843.1:p.Lys171=
XM_011518348.1:c.465G>A	XP_011516650.1:p.Lys155=
XM_011518349.1:c.285G>A	XP_011516651.1:p.Lys95=
NM_001318121.1:c.465G>A	NP_001305050.1:p.Lys155=
NM_001318122.1:c.513G>A	NP_001305051.1:p.Lys171=
XM_017014428.1:c.465G>A	XP_016869917.1:p.Lys155=
XM_024447439.1:c.444G>A	XP_024303207.1:p.Lys148=
XM_024447440.1:c.285G>A	XP_024303208.1:p.Lys95=
NM_001318122.2:c.513G>A	NP_001305051.1:p.Lys171=
NM_000476.3:c.465G>A MANE Select	NP_000467.1:p.Lys155=
NR_174625.1:n.3784G>A
NR_174626.1:n.3627G>A
NR_174627.1:n.3664G>A
NR_174628.1:n.3042G>A
NR_174629.1:n.2987G>A
NR_174630.1:n.3023G>A
NR_174631.1:n.2968G>A
NR_174632.1:n.3057G>A