Canonical Allele Identifier: CA1364649052

Gene: ACY1 ABHD14A-ACY1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.51986990G= , CM000665.2:g.51986990G=	GRCh38
NC_000003.11:g.52021006G= , CM000665.1:g.52021006G=	GRCh37
NC_000003.10:g.51996046G=	NCBI36
NG_012036.1:g.8444G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404366.7:c.586G= (ACY1)	ENSP00000384296.2:p.Val196=
ENST00000464587.2:n.272G= (ACY1)
ENST00000486081.6:c.*432G= (ABHD14A-ACY1)	ENSP00000420395.1:n.*432G=
ENST00000635785.1:c.816G= (ABHD14A-ACY1)
ENST00000635797.1:c.481G= (ACY1)	ENSP00000490007.1:p.Val161=
ENST00000635937.1:c.*758G= (ABHD14A-ACY1)	ENSP00000489887.1:n.*758G=
ENST00000635941.1:c.775G= (ACY1)	ENSP00000490309.1:n.775G=
ENST00000635946.1:c.*858G= (ABHD14A-ACY1)	ENSP00000490284.1:n.*858G=
ENST00000635951.1:c.*858G= (ABHD14A-ACY1)	ENSP00000490649.1:n.*858G=
ENST00000635952.1:c.673G= (ABHD14A-ACY1)	ENSP00000490434.1:p.Val225=
ENST00000636085.1:c.*432G= (ABHD14A-ACY1)	ENSP00000489981.1:n.*432G=
ENST00000636089.1:c.*923G= (ABHD14A-ACY1)	ENSP00000490657.1:n.*923G=
ENST00000636358.2:c.586G= (ACY1) MANE Select	ENSP00000490149.1:p.Val196=
ENST00000636490.1:c.*923G= (ABHD14A-ACY1)	ENSP00000490575.1:n.*923G=
ENST00000636556.1:c.*531G= (ACY1)	ENSP00000490500.1:n.*531G=
ENST00000636646.1:c.*823G= (ABHD14A-ACY1)	ENSP00000490688.1:n.*823G=
ENST00000636660.1:c.464G= (ABHD14A-ACY1)
ENST00000636718.1:c.*1113G= (ABHD14A-ACY1)	ENSP00000490429.1:n.*1113G=
ENST00000636826.1:c.*432G= (ABHD14A-ACY1)	ENSP00000489721.1:n.*432G=
ENST00000636880.1:c.*296G= (ACY1)	ENSP00000489947.1:n.*296G=
ENST00000636942.1:c.*467G= (ABHD14A-ACY1)	ENSP00000490848.1:n.*467G=
ENST00000637025.1:c.*622G= (ABHD14A-ACY1)	ENSP00000490236.1:n.*622G=
ENST00000637130.1:c.*722G= (ABHD14A-ACY1)	ENSP00000490887.1:n.*722G=
ENST00000637199.1:n.59G= (ACY1)
ENST00000637209.1:c.*296G= (ACY1)	ENSP00000490708.1:n.*296G=
ENST00000637222.1:c.586G= (ABHD14A-ACY1)	ENSP00000490353.1:p.Val196=
ENST00000637251.1:n.1659G= (ACY1)
ENST00000637349.1:c.*149G= (ACY1)	ENSP00000489688.1:n.*149G=
ENST00000637460.1:n.620G= (ACY1)
ENST00000637461.1:c.433G= (ABHD14A-ACY1)
ENST00000637512.1:c.751G= (ABHD14A-ACY1)
ENST00000637563.1:c.*1249G= (ABHD14A-ACY1)	ENSP00000490319.1:n.*1249G=
ENST00000637696.1:c.*858G= (ABHD14A-ACY1)	ENSP00000490554.1:n.*858G=
ENST00000637730.1:c.1119G= (ABHD14A-ACY1)
ENST00000637778.1:c.*1249G= (ABHD14A-ACY1)	ENSP00000490052.1:n.*1249G=
ENST00000637978.1:c.1155G= (ABHD14A-ACY1)
ENST00000638096.1:n.392G= (ACY1)
ENST00000638136.1:n.917G= (ACY1)
ENST00000404366.6:c.586G= (ACY1)	ENSP00000384296.2:p.Val196=
ENST00000463721.5:c.*497G= (ABHD14A-ACY1)	ENSP00000417688.1:n.*497G=
ENST00000463937.1:c.889G= (ABHD14A-ACY1)	ENSP00000420487.1:p.Val297=
ENST00000464587.1:n.272G= (ACY1)
ENST00000465121.5:n.659G= (ACY1)
ENST00000469863.1:c.613G= (ACY1)	ENSP00000419830.1:p.Val205=
ENST00000476351.5:c.481G= (ACY1)	ENSP00000417056.1:p.Val161=
ENST00000476854.5:c.586G= (ACY1)	ENSP00000419262.1:p.Val196=
ENST00000491318.5:c.584-319G= (ACY1)	ENSP00000418683.1:n.584-319G=
ENST00000494103.5:c.370G= (ACY1)	ENSP00000417618.1:p.Val124=
NM_000666.2:c.586G= (ACY1)	NP_000657.1:p.Val196=
NM_001198895.1:c.586G= (ACY1)	NP_001185824.1:p.Val196=
NM_001198896.1:c.370G= (ACY1)	NP_001185825.1:p.Val124=
NM_001198897.1:c.586G= (ACY1)	NP_001185826.1:p.Val196=
NM_001198898.1:c.481G= (ACY1)	NP_001185827.1:p.Val161=
NM_001316331.1:c.856G= (ABHD14A-ACY1)	NP_001303260.1:p.Val286=
NM_000666.3:c.586G= (ACY1) MANE Select	NP_000657.1:p.Val196=
NM_001198895.2:c.586G= (ACY1)	NP_001185824.1:p.Val196=
NM_001198896.2:c.370G= (ACY1)	NP_001185825.1:p.Val124=
NM_001198897.2:c.586G= (ACY1)	NP_001185826.1:p.Val196=
NM_001198898.2:c.481G= (ACY1)	NP_001185827.1:p.Val161=
NM_001316331.2:c.856G= (ABHD14A-ACY1)	NP_001303260.1:p.Val286=