Canonical Allele Identifier: CA1364649129
Gene: ACY1 HGNC NCBI
ABHD14A-ACY1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.51987176C= , CM000665.2:g.51987176C= GRCh38
NC_000003.11:g.52021192C= , CM000665.1:g.52021192C= GRCh37
NC_000003.10:g.51996232C= NCBI36
NG_012036.1:g.8630C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000404366.7:c.687C= (ACY1) ENSP00000384296.2:p.Phe229=
ENST00000464587.2:n.373C= (ACY1)
ENST00000486081.6:c.*533C= (ABHD14A-ACY1) ENSP00000420395.1:n.*533C=
ENST00000635785.1:c.887+115C= (ABHD14A-ACY1)
ENST00000635797.1:c.582C= (ACY1) ENSP00000490007.1:p.Phe194=
ENST00000635937.1:c.*944C= (ABHD14A-ACY1) ENSP00000489887.1:n.*944C=
ENST00000635941.1:c.961C= (ACY1) ENSP00000490309.1:n.961C=
ENST00000635946.1:c.*1044C= (ABHD14A-ACY1) ENSP00000490284.1:n.*1044C=
ENST00000635951.1:c.*959C= (ABHD14A-ACY1) ENSP00000490649.1:n.*959C=
ENST00000635952.1:c.774C= (ABHD14A-ACY1) ENSP00000490434.1:p.Phe258=
ENST00000636085.1:c.*618C= (ABHD14A-ACY1) ENSP00000489981.1:n.*618C=
ENST00000636089.1:c.*1024C= (ABHD14A-ACY1) ENSP00000490657.1:n.*1024C=
ENST00000636358.2:c.687C= (ACY1) MANE Select ENSP00000490149.1:p.Phe229=
ENST00000636490.1:c.*1024C= (ABHD14A-ACY1) ENSP00000490575.1:n.*1024C=
ENST00000636556.1:c.*632C= (ACY1) ENSP00000490500.1:n.*632C=
ENST00000636646.1:c.*924C= (ABHD14A-ACY1) ENSP00000490688.1:n.*924C=
ENST00000636660.1:c.650C= (ABHD14A-ACY1)
ENST00000636718.1:c.*1299C= (ABHD14A-ACY1) ENSP00000490429.1:n.*1299C=
ENST00000636826.1:c.*618C= (ABHD14A-ACY1) ENSP00000489721.1:n.*618C=
ENST00000636880.1:c.*397C= (ACY1) ENSP00000489947.1:n.*397C=
ENST00000636942.1:c.*568C= (ABHD14A-ACY1) ENSP00000490848.1:n.*568C=
ENST00000637025.1:c.*808C= (ABHD14A-ACY1) ENSP00000490236.1:n.*808C=
ENST00000637034.1:n.120C= (ACY1)
ENST00000637130.1:c.*908C= (ABHD14A-ACY1) ENSP00000490887.1:n.*908C=
ENST00000637199.1:n.160C= (ACY1)
ENST00000637222.1:c.687C= (ABHD14A-ACY1) ENSP00000490353.1:p.Phe229=
ENST00000637349.1:c.*220+115C= (ACY1) ENSP00000489688.1:n.*220+115C=
ENST00000637460.1:n.721C= (ACY1)
ENST00000637512.1:c.937C= (ABHD14A-ACY1)
ENST00000637563.1:c.*1435C= (ABHD14A-ACY1) ENSP00000490319.1:n.*1435C=
ENST00000637696.1:c.*1044C= (ABHD14A-ACY1) ENSP00000490554.1:n.*1044C=
ENST00000637730.1:c.1220C= (ABHD14A-ACY1)
ENST00000637778.1:c.*1435C= (ABHD14A-ACY1) ENSP00000490052.1:n.*1435C=
ENST00000637978.1:c.1256C= (ABHD14A-ACY1)
ENST00000638096.1:n.578C= (ACY1)
ENST00000638136.1:n.1103C= (ACY1)
ENST00000404366.6:c.687C= (ACY1) ENSP00000384296.2:p.Phe229=
ENST00000463721.5:c.*598C= (ABHD14A-ACY1) ENSP00000417688.1:n.*598C=
ENST00000463937.1:c.990C= (ABHD14A-ACY1) ENSP00000420487.1:p.Phe330=
ENST00000464587.1:n.373C= (ACY1)
ENST00000465121.5:n.760C= (ACY1)
ENST00000476351.5:c.582C= (ACY1) ENSP00000417056.1:p.Phe194=
ENST00000476854.5:c.657+115C= (ACY1) ENSP00000419262.1:n.657+115C=
ENST00000491318.5:c.584-133C= (ACY1) ENSP00000418683.1:n.584-133C=
ENST00000494103.5:c.471C= (ACY1) ENSP00000417618.1:p.Phe157=
NM_000666.2:c.687C= (ACY1) NP_000657.1:p.Phe229=
NM_001198895.1:c.687C= (ACY1) NP_001185824.1:p.Phe229=
NM_001198896.1:c.471C= (ACY1) NP_001185825.1:p.Phe157=
NM_001198897.1:c.657+115C= (ACY1) NP_001185826.1:n.657+115C=
NM_001198898.1:c.582C= (ACY1) NP_001185827.1:p.Phe194=
NM_001316331.1:c.957C= (ABHD14A-ACY1) NP_001303260.1:p.Phe319=
NM_000666.3:c.687C= (ACY1) MANE Select NP_000657.1:p.Phe229=
NM_001198895.2:c.687C= (ACY1) NP_001185824.1:p.Phe229=
NM_001198896.2:c.471C= (ACY1) NP_001185825.1:p.Phe157=
NM_001198897.2:c.657+115C= (ACY1) NP_001185826.1:n.657+115C=
NM_001198898.2:c.582C= (ACY1) NP_001185827.1:p.Phe194=
NM_001316331.2:c.957C= (ABHD14A-ACY1) NP_001303260.1:p.Phe319=