Canonical Allele Identifier: CA433748868

Gene: ACY1 ABHD14A-ACY1

Linked Data

• MyVariant Identifiers: chr3:g.52021023T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.51987007T>A , CM000665.2:g.51987007T>A	GRCh38
NC_000003.11:g.52021023T>A , CM000665.1:g.52021023T>A	GRCh37
NC_000003.10:g.51996063T>A	NCBI36
NG_012036.1:g.8461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404366.7:c.603T>A (ACY1)	ENSP00000384296.2:p.Thr201=
ENST00000464587.2:n.289T>A (ACY1)
ENST00000486081.6:c.*449T>A (ABHD14A-ACY1)	ENSP00000420395.1:n.*449T>A
ENST00000635785.1:c.833T>A (ABHD14A-ACY1)
ENST00000635797.1:c.498T>A (ACY1)	ENSP00000490007.1:p.Thr166=
ENST00000635937.1:c.*775T>A (ABHD14A-ACY1)	ENSP00000489887.1:n.*775T>A
ENST00000635941.1:c.792T>A (ACY1)	ENSP00000490309.1:n.792T>A
ENST00000635946.1:c.*875T>A (ABHD14A-ACY1)	ENSP00000490284.1:n.*875T>A
ENST00000635951.1:c.*875T>A (ABHD14A-ACY1)	ENSP00000490649.1:n.*875T>A
ENST00000635952.1:c.690T>A (ABHD14A-ACY1)	ENSP00000490434.1:p.Thr230=
ENST00000636085.1:c.*449T>A (ABHD14A-ACY1)	ENSP00000489981.1:n.*449T>A
ENST00000636089.1:c.*940T>A (ABHD14A-ACY1)	ENSP00000490657.1:n.*940T>A
ENST00000636358.2:c.603T>A (ACY1) MANE Select	ENSP00000490149.1:p.Thr201=
ENST00000636490.1:c.*940T>A (ABHD14A-ACY1)	ENSP00000490575.1:n.*940T>A
ENST00000636556.1:c.*548T>A (ACY1)	ENSP00000490500.1:n.*548T>A
ENST00000636646.1:c.*840T>A (ABHD14A-ACY1)	ENSP00000490688.1:n.*840T>A
ENST00000636660.1:c.481T>A (ABHD14A-ACY1)
ENST00000636718.1:c.*1130T>A (ABHD14A-ACY1)	ENSP00000490429.1:n.*1130T>A
ENST00000636826.1:c.*449T>A (ABHD14A-ACY1)	ENSP00000489721.1:n.*449T>A
ENST00000636880.1:c.*313T>A (ACY1)	ENSP00000489947.1:n.*313T>A
ENST00000636942.1:c.*484T>A (ABHD14A-ACY1)	ENSP00000490848.1:n.*484T>A
ENST00000637025.1:c.*639T>A (ABHD14A-ACY1)	ENSP00000490236.1:n.*639T>A
ENST00000637130.1:c.*739T>A (ABHD14A-ACY1)	ENSP00000490887.1:n.*739T>A
ENST00000637199.1:n.76T>A (ACY1)
ENST00000637209.1:c.*313T>A (ACY1)	ENSP00000490708.1:n.*313T>A
ENST00000637222.1:c.603T>A (ABHD14A-ACY1)	ENSP00000490353.1:p.Thr201=
ENST00000637251.1:n.1676T>A (ACY1)
ENST00000637349.1:c.*166T>A (ACY1)	ENSP00000489688.1:n.*166T>A
ENST00000637460.1:n.637T>A (ACY1)
ENST00000637461.1:c.450T>A (ABHD14A-ACY1)
ENST00000637512.1:c.768T>A (ABHD14A-ACY1)
ENST00000637563.1:c.*1266T>A (ABHD14A-ACY1)	ENSP00000490319.1:n.*1266T>A
ENST00000637696.1:c.*875T>A (ABHD14A-ACY1)	ENSP00000490554.1:n.*875T>A
ENST00000637730.1:c.1136T>A (ABHD14A-ACY1)
ENST00000637778.1:c.*1266T>A (ABHD14A-ACY1)	ENSP00000490052.1:n.*1266T>A
ENST00000637978.1:c.1172T>A (ABHD14A-ACY1)
ENST00000638096.1:n.409T>A (ACY1)
ENST00000638136.1:n.934T>A (ACY1)
ENST00000404366.6:c.603T>A (ACY1)	ENSP00000384296.2:p.Thr201=
ENST00000463721.5:c.*514T>A (ABHD14A-ACY1)	ENSP00000417688.1:n.*514T>A
ENST00000463937.1:c.906T>A (ABHD14A-ACY1)	ENSP00000420487.1:p.Thr302=
ENST00000464587.1:n.289T>A (ACY1)
ENST00000465121.5:n.676T>A (ACY1)
ENST00000469863.1:c.630T>A (ACY1)	ENSP00000419830.1:p.Thr210=
ENST00000476351.5:c.498T>A (ACY1)	ENSP00000417056.1:p.Thr166=
ENST00000476854.5:c.603T>A (ACY1)	ENSP00000419262.1:p.Thr201=
ENST00000491318.5:c.584-302T>A (ACY1)	ENSP00000418683.1:n.584-302T>A
ENST00000494103.5:c.387T>A (ACY1)	ENSP00000417618.1:p.Thr129=
NM_000666.2:c.603T>A (ACY1)	NP_000657.1:p.Thr201=
NM_001198895.1:c.603T>A (ACY1)	NP_001185824.1:p.Thr201=
NM_001198896.1:c.387T>A (ACY1)	NP_001185825.1:p.Thr129=
NM_001198897.1:c.603T>A (ACY1)	NP_001185826.1:p.Thr201=
NM_001198898.1:c.498T>A (ACY1)	NP_001185827.1:p.Thr166=
NM_001316331.1:c.873T>A (ABHD14A-ACY1)	NP_001303260.1:p.Thr291=
NM_000666.3:c.603T>A (ACY1) MANE Select	NP_000657.1:p.Thr201=
NM_001198895.2:c.603T>A (ACY1)	NP_001185824.1:p.Thr201=
NM_001198896.2:c.387T>A (ACY1)	NP_001185825.1:p.Thr129=
NM_001198897.2:c.603T>A (ACY1)	NP_001185826.1:p.Thr201=
NM_001198898.2:c.498T>A (ACY1)	NP_001185827.1:p.Thr166=
NM_001316331.2:c.873T>A (ABHD14A-ACY1)	NP_001303260.1:p.Thr291=