Canonical Allele Identifier: CA1364649079
Gene: ACY1 HGNC NCBI
ABHD14A-ACY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.51987055G= , CM000665.2:g.51987055G= GRCh38
NC_000003.11:g.52021071G= , CM000665.1:g.52021071G= GRCh37
NC_000003.10:g.51996111G= NCBI36
NG_012036.1:g.8509G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404366.7:c.651G= (ACY1) ENSP00000384296.2:p.Glu217=
ENST00000464587.2:n.337G= (ACY1)
ENST00000486081.6:c.*497G= (ABHD14A-ACY1) ENSP00000420395.1:n.*497G=
ENST00000635785.1:c.881G= (ABHD14A-ACY1)
ENST00000635797.1:c.546G= (ACY1) ENSP00000490007.1:p.Glu182=
ENST00000635937.1:c.*823G= (ABHD14A-ACY1) ENSP00000489887.1:n.*823G=
ENST00000635941.1:c.840G= (ACY1) ENSP00000490309.1:n.840G=
ENST00000635946.1:c.*923G= (ABHD14A-ACY1) ENSP00000490284.1:n.*923G=
ENST00000635951.1:c.*923G= (ABHD14A-ACY1) ENSP00000490649.1:n.*923G=
ENST00000635952.1:c.738G= (ABHD14A-ACY1) ENSP00000490434.1:p.Glu246=
ENST00000636085.1:c.*497G= (ABHD14A-ACY1) ENSP00000489981.1:n.*497G=
ENST00000636089.1:c.*988G= (ABHD14A-ACY1) ENSP00000490657.1:n.*988G=
ENST00000636358.2:c.651G= (ACY1) MANE Select ENSP00000490149.1:p.Glu217=
ENST00000636490.1:c.*988G= (ABHD14A-ACY1) ENSP00000490575.1:n.*988G=
ENST00000636556.1:c.*596G= (ACY1) ENSP00000490500.1:n.*596G=
ENST00000636646.1:c.*888G= (ABHD14A-ACY1) ENSP00000490688.1:n.*888G=
ENST00000636660.1:c.529G= (ABHD14A-ACY1)
ENST00000636718.1:c.*1178G= (ABHD14A-ACY1) ENSP00000490429.1:n.*1178G=
ENST00000636826.1:c.*497G= (ABHD14A-ACY1) ENSP00000489721.1:n.*497G=
ENST00000636880.1:c.*361G= (ACY1) ENSP00000489947.1:n.*361G=
ENST00000636942.1:c.*532G= (ABHD14A-ACY1) ENSP00000490848.1:n.*532G=
ENST00000637025.1:c.*687G= (ABHD14A-ACY1) ENSP00000490236.1:n.*687G=
ENST00000637130.1:c.*787G= (ABHD14A-ACY1) ENSP00000490887.1:n.*787G=
ENST00000637199.1:n.124G= (ACY1)
ENST00000637209.1:c.*361G= (ACY1) ENSP00000490708.1:n.*361G=
ENST00000637222.1:c.651G= (ABHD14A-ACY1) ENSP00000490353.1:p.Glu217=
ENST00000637251.1:n.1724G= (ACY1)
ENST00000637349.1:c.*214G= (ACY1) ENSP00000489688.1:n.*214G=
ENST00000637460.1:n.685G= (ACY1)
ENST00000637461.1:c.498G= (ABHD14A-ACY1)
ENST00000637512.1:c.816G= (ABHD14A-ACY1)
ENST00000637563.1:c.*1314G= (ABHD14A-ACY1) ENSP00000490319.1:n.*1314G=
ENST00000637696.1:c.*923G= (ABHD14A-ACY1) ENSP00000490554.1:n.*923G=
ENST00000637730.1:c.1184G= (ABHD14A-ACY1)
ENST00000637778.1:c.*1314G= (ABHD14A-ACY1) ENSP00000490052.1:n.*1314G=
ENST00000637978.1:c.1220G= (ABHD14A-ACY1)
ENST00000638096.1:n.457G= (ACY1)
ENST00000638136.1:n.982G= (ACY1)
ENST00000404366.6:c.651G= (ACY1) ENSP00000384296.2:p.Glu217=
ENST00000463721.5:c.*562G= (ABHD14A-ACY1) ENSP00000417688.1:n.*562G=
ENST00000463937.1:c.954G= (ABHD14A-ACY1) ENSP00000420487.1:p.Glu318=
ENST00000464587.1:n.337G= (ACY1)
ENST00000465121.5:n.724G= (ACY1)
ENST00000469863.1:c.678G= (ACY1) ENSP00000419830.1:p.Glu226=
ENST00000476351.5:c.546G= (ACY1) ENSP00000417056.1:p.Glu182=
ENST00000476854.5:c.651G= (ACY1) ENSP00000419262.1:p.Glu217=
ENST00000491318.5:c.584-254G= (ACY1) ENSP00000418683.1:n.584-254G=
ENST00000494103.5:c.435G= (ACY1) ENSP00000417618.1:p.Glu145=
NM_000666.2:c.651G= (ACY1) NP_000657.1:p.Glu217=
NM_001198895.1:c.651G= (ACY1) NP_001185824.1:p.Glu217=
NM_001198896.1:c.435G= (ACY1) NP_001185825.1:p.Glu145=
NM_001198897.1:c.651G= (ACY1) NP_001185826.1:p.Glu217=
NM_001198898.1:c.546G= (ACY1) NP_001185827.1:p.Glu182=
NM_001316331.1:c.921G= (ABHD14A-ACY1) NP_001303260.1:p.Glu307=
NM_000666.3:c.651G= (ACY1) MANE Select NP_000657.1:p.Glu217=
NM_001198895.2:c.651G= (ACY1) NP_001185824.1:p.Glu217=
NM_001198896.2:c.435G= (ACY1) NP_001185825.1:p.Glu145=
NM_001198897.2:c.651G= (ACY1) NP_001185826.1:p.Glu217=
NM_001198898.2:c.546G= (ACY1) NP_001185827.1:p.Glu182=
NM_001316331.2:c.921G= (ABHD14A-ACY1) NP_001303260.1:p.Glu307=