Canonical Allele Identifier: CA374947158

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630670C>G (hg19) ; chr9:g.127868391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868391C>G , CM000671.2:g.127868391C>G	GRCh38
NC_000009.11:g.130630670C>G , CM000671.1:g.130630670C>G	GRCh37
NC_000009.10:g.129670491C>G	NCBI36
NG_011792.1:g.14353G>C
NG_011792.2:g.14353G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.946G>C
ENST00000643029.1:c.*2121G>C	ENSP00000496586.1:n.*2121G>C
ENST00000643338.1:c.*2010G>C	ENSP00000495890.1:n.*2010G>C
ENST00000644144.2:c.446G>C MANE Select	ENSP00000494600.1:p.Arg149Pro
ENST00000645007.1:c.*2370G>C	ENSP00000494773.1:n.*2370G>C
ENST00000646171.1:c.*479G>C	ENSP00000495484.1:n.*479G>C
ENST00000223836.10:c.494G>C	ENSP00000223836.10:p.Arg165Pro
ENST00000373156.5:c.446G>C	ENSP00000362249.1:p.Arg149Pro
ENST00000373176.5:c.446G>C	ENSP00000362271.1:p.Arg149Pro
ENST00000413016.5:c.268G>C
ENST00000550143.5:c.226G>C	ENSP00000449130.1:n.226G>C
NM_000476.2:c.446G>C	NP_000467.1:p.Arg149Pro
XM_005251786.2:c.494G>C	XP_005251843.1:p.Arg165Pro
XM_011518348.1:c.446G>C	XP_011516650.1:p.Arg149Pro
XM_011518349.1:c.266G>C	XP_011516651.1:p.Arg89Pro
NM_001318121.1:c.446G>C	NP_001305050.1:p.Arg149Pro
NM_001318122.1:c.494G>C	NP_001305051.1:p.Arg165Pro
XM_017014428.1:c.446G>C	XP_016869917.1:p.Arg149Pro
XM_024447439.1:c.425G>C	XP_024303207.1:p.Arg142Pro
XM_024447440.1:c.266G>C	XP_024303208.1:p.Arg89Pro
NM_001318122.2:c.494G>C	NP_001305051.1:p.Arg165Pro
NM_000476.3:c.446G>C MANE Select	NP_000467.1:p.Arg149Pro
NR_174625.1:n.3765G>C
NR_174626.1:n.3608G>C
NR_174627.1:n.3645G>C
NR_174628.1:n.3023G>C
NR_174629.1:n.2968G>C
NR_174630.1:n.3004G>C
NR_174631.1:n.2949G>C
NR_174632.1:n.3038G>C