Canonical Allele Identifier: CA1360909816
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43699333T= , CM000665.2:g.43699333T= GRCh38
NC_000003.11:g.43740825T= , CM000665.1:g.43740825T= GRCh37
NC_000003.10:g.43715829T= NCBI36
NG_007090.3:g.13451T=
NG_007090.5:g.13464T=

Transcript Alleles

HGVS Amino-acid change
ENST00000013894.3:c.105T= ENSP00000013894.2:p.Leu35=
ENST00000454293.2:c.-19T= ENSP00000412014.2:n.-19T=
ENST00000458276.7:c.105T= ENSP00000390849.3:p.Leu35=
ENST00000642351.1:c.-19T= ENSP00000494478.1:n.-19T=
ENST00000643140.1:c.105T= ENSP00000495588.1:p.Leu35=
ENST00000643477.1:c.105T= ENSP00000496220.1:p.Leu35=
ENST00000643500.1:c.105T= ENSP00000494735.1:p.Leu35=
ENST00000643520.1:n.153T=
ENST00000644371.2:c.105T= MANE Select ENSP00000495778.1:p.Leu35=
ENST00000646378.1:c.*155T= ENSP00000495826.1:n.*155T=
ENST00000646799.1:c.105T= ENSP00000494829.1:p.Leu35=
ENST00000649763.1:c.105T= ENSP00000497701.1:p.Leu35=
ENST00000013894.2:c.105T= ENSP00000013894.2:p.Leu35=
ENST00000454293.1:c.-19T= ENSP00000412014.1:n.-19T=
ENST00000456453.5:c.-19T= ENSP00000391582.1:n.-19T=
ENST00000458276.6:c.105T= ENSP00000390849.2:p.Leu35=
ENST00000486764.1:n.206T=
NM_016006.4:c.105T= NP_057090.2:p.Leu35=
XM_011533779.1:c.-19T= XP_011532081.1:n.-19T=
XM_011533780.1:c.105T= XP_011532082.1:p.Leu35=
XR_940447.1:n.162T=
NM_001355186.1:c.105T= NP_001342115.1:p.Leu35=
NM_001365649.1:c.-19T= NP_001352578.1:n.-19T=
NM_001365650.1:c.105T= NP_001352579.1:p.Leu35=
NM_016006.5:c.105T= NP_057090.2:p.Leu35=
NR_158560.1:n.228T=
NM_001355186.2:c.105T= NP_001342115.1:p.Leu35=
NM_016006.6:c.105T= MANE Select NP_057090.2:p.Leu35=