Canonical Allele Identifier: CA467223599

Gene: AK1

Linked Data

• gnomAD v4: 9-127868390-C-A
• MyVariant Identifiers: chr9:g.130630669C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868390C>A , CM000671.2:g.127868390C>A	GRCh38
NC_000009.11:g.130630669C>A , CM000671.1:g.130630669C>A	GRCh37
NC_000009.10:g.129670490C>A	NCBI36
NG_011792.1:g.14354G>T
NG_011792.2:g.14354G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.947G>T
ENST00000643029.1:c.*2122G>T	ENSP00000496586.1:n.*2122G>T
ENST00000643338.1:c.*2011G>T	ENSP00000495890.1:n.*2011G>T
ENST00000644144.2:c.447G>T MANE Select	ENSP00000494600.1:p.Arg149=
ENST00000645007.1:c.*2371G>T	ENSP00000494773.1:n.*2371G>T
ENST00000646171.1:c.*480G>T	ENSP00000495484.1:n.*480G>T
ENST00000223836.10:c.495G>T	ENSP00000223836.10:p.Arg165=
ENST00000373156.5:c.447G>T	ENSP00000362249.1:p.Arg149=
ENST00000373176.5:c.447G>T	ENSP00000362271.1:p.Arg149=
ENST00000413016.5:c.269G>T
ENST00000550143.5:c.227G>T	ENSP00000449130.1:n.227G>T
NM_000476.2:c.447G>T	NP_000467.1:p.Arg149=
XM_005251786.2:c.495G>T	XP_005251843.1:p.Arg165=
XM_011518348.1:c.447G>T	XP_011516650.1:p.Arg149=
XM_011518349.1:c.267G>T	XP_011516651.1:p.Arg89=
NM_001318121.1:c.447G>T	NP_001305050.1:p.Arg149=
NM_001318122.1:c.495G>T	NP_001305051.1:p.Arg165=
XM_017014428.1:c.447G>T	XP_016869917.1:p.Arg149=
XM_024447439.1:c.426G>T	XP_024303207.1:p.Arg142=
XM_024447440.1:c.267G>T	XP_024303208.1:p.Arg89=
NM_001318122.2:c.495G>T	NP_001305051.1:p.Arg165=
NM_000476.3:c.447G>T MANE Select	NP_000467.1:p.Arg149=
NR_174625.1:n.3766G>T
NR_174626.1:n.3609G>T
NR_174627.1:n.3646G>T
NR_174628.1:n.3024G>T
NR_174629.1:n.2969G>T
NR_174630.1:n.3005G>T
NR_174631.1:n.2950G>T
NR_174632.1:n.3039G>T