Canonical Allele Identifier: CA1360917177
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717815C= , CM000665.2:g.43717815C= GRCh38
NC_000003.11:g.43759307C= , CM000665.1:g.43759307C= GRCh37
NC_000003.10:g.43734311C= NCBI36
NG_007090.3:g.31933C=
NG_007090.5:g.31946C=

Transcript Alleles

HGVS Amino-acid change
ENST00000413300.2:c.317C=
ENST00000454293.2:c.795C= ENSP00000412014.2:p.Thr265=
ENST00000458276.7:c.774-628C= ENSP00000390849.3:n.774-628C=
ENST00000463153.2:c.145C=
ENST00000642351.1:c.795C= ENSP00000494478.1:p.Thr265=
ENST00000643140.1:c.*280C= ENSP00000495588.1:n.*280C=
ENST00000643477.1:c.*379C= ENSP00000496220.1:n.*379C=
ENST00000643500.1:c.*119C= ENSP00000494735.1:n.*119C=
ENST00000643520.1:n.1084C=
ENST00000644371.2:c.918C= MANE Select ENSP00000495778.1:p.Thr306=
ENST00000646378.1:c.*968C= ENSP00000495826.1:n.*968C=
ENST00000646799.1:c.*248-628C= ENSP00000494829.1:n.*248-628C=
ENST00000649763.1:c.918C= ENSP00000497701.1:p.Thr306=
ENST00000413300.1:c.319C= ENSP00000392159.1:p.Gln107=
ENST00000458276.6:c.918C= ENSP00000390849.2:p.Thr306=
ENST00000463153.1:n.148C=
NM_016006.4:c.918C= NP_057090.2:p.Thr306=
XM_011533779.1:c.795C= XP_011532081.1:p.Thr265=
XM_011533780.1:c.774-628C= XP_011532082.1:n.774-628C=
XR_940447.1:n.863C=
NM_001355186.1:c.918C= NP_001342115.1:p.Thr306=
NM_001365649.1:c.795C= NP_001352578.1:p.Thr265=
NM_001365650.1:c.774-628C= NP_001352579.1:n.774-628C=
NM_016006.5:c.918C= NP_057090.2:p.Thr306=
NR_158560.1:n.929C=
NM_001355186.2:c.918C= NP_001342115.1:p.Thr306=
NM_016006.6:c.918C= MANE Select NP_057090.2:p.Thr306=