Canonical Allele Identifier: CA374947328

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630697T>G (hg19) ; chr9:g.127868418T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868418T>G , CM000671.2:g.127868418T>G	GRCh38
NC_000009.11:g.130630697T>G , CM000671.1:g.130630697T>G	GRCh37
NC_000009.10:g.129670518T>G	NCBI36
NG_011792.1:g.14326A>C
NG_011792.2:g.14326A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.919A>C
ENST00000643029.1:c.*2094A>C	ENSP00000496586.1:n.*2094A>C
ENST00000643338.1:c.*1983A>C	ENSP00000495890.1:n.*1983A>C
ENST00000644144.2:c.419A>C MANE Select	ENSP00000494600.1:p.Asp140Ala
ENST00000645007.1:c.*2343A>C	ENSP00000494773.1:n.*2343A>C
ENST00000646171.1:c.*452A>C	ENSP00000495484.1:n.*452A>C
ENST00000223836.10:c.467A>C	ENSP00000223836.10:p.Asp156Ala
ENST00000373156.5:c.419A>C	ENSP00000362249.1:p.Asp140Ala
ENST00000373176.5:c.419A>C	ENSP00000362271.1:p.Asp140Ala
ENST00000413016.5:c.241A>C
ENST00000550143.5:c.199A>C	ENSP00000449130.1:n.199A>C
NM_000476.2:c.419A>C	NP_000467.1:p.Asp140Ala
XM_005251786.2:c.467A>C	XP_005251843.1:p.Asp156Ala
XM_011518348.1:c.419A>C	XP_011516650.1:p.Asp140Ala
XM_011518349.1:c.239A>C	XP_011516651.1:p.Asp80Ala
NM_001318121.1:c.419A>C	NP_001305050.1:p.Asp140Ala
NM_001318122.1:c.467A>C	NP_001305051.1:p.Asp156Ala
XM_017014428.1:c.419A>C	XP_016869917.1:p.Asp140Ala
XM_024447439.1:c.398A>C	XP_024303207.1:p.Asp133Ala
XM_024447440.1:c.239A>C	XP_024303208.1:p.Asp80Ala
NM_001318122.2:c.467A>C	NP_001305051.1:p.Asp156Ala
NM_000476.3:c.419A>C MANE Select	NP_000467.1:p.Asp140Ala
NR_174625.1:n.3738A>C
NR_174626.1:n.3581A>C
NR_174627.1:n.3618A>C
NR_174628.1:n.2996A>C
NR_174629.1:n.2941A>C
NR_174630.1:n.2977A>C
NR_174631.1:n.2922A>C
NR_174632.1:n.3011A>C