Canonical Allele Identifier: CA1360917104
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717640A= , CM000665.2:g.43717640A= GRCh38
NC_000003.11:g.43759132A= , CM000665.1:g.43759132A= GRCh37
NC_000003.10:g.43734136A= NCBI36
NG_007090.3:g.31758A=
NG_007090.5:g.31771A=

Transcript Alleles

HGVS Amino-acid change
ENST00000413300.2:c.268-126A=
ENST00000454293.2:c.651-31A= ENSP00000412014.2:n.651-31A=
ENST00000458276.7:c.774-803A= ENSP00000390849.3:n.774-803A=
ENST00000642351.1:c.651-31A= ENSP00000494478.1:n.651-31A=
ENST00000643140.1:c.*136-31A= ENSP00000495588.1:n.*136-31A=
ENST00000643477.1:c.*235-31A= ENSP00000496220.1:n.*235-31A=
ENST00000643500.1:c.662-31A= ENSP00000494735.1:n.662-31A=
ENST00000643520.1:n.940-31A=
ENST00000644371.2:c.774-31A= MANE Select ENSP00000495778.1:n.774-31A=
ENST00000646378.1:c.*824-31A= ENSP00000495826.1:n.*824-31A=
ENST00000646799.1:c.*248-803A= ENSP00000494829.1:n.*248-803A=
ENST00000649763.1:c.774-31A= ENSP00000497701.1:n.774-31A=
ENST00000413300.1:c.270-126A= ENSP00000392159.1:n.270-126A=
ENST00000458276.6:c.774-31A= ENSP00000390849.2:n.774-31A=
NM_016006.4:c.774-31A= NP_057090.2:n.774-31A=
XM_011533779.1:c.651-31A= XP_011532081.1:n.651-31A=
XM_011533780.1:c.774-803A= XP_011532082.1:n.774-803A=
XR_940447.1:n.719-31A=
NM_001355186.1:c.774-31A= NP_001342115.1:n.774-31A=
NM_001365649.1:c.651-31A= NP_001352578.1:n.651-31A=
NM_001365650.1:c.774-803A= NP_001352579.1:n.774-803A=
NM_016006.5:c.774-31A= NP_057090.2:n.774-31A=
NR_158560.1:n.785-31A=
NM_001355186.2:c.774-31A= NP_001342115.1:n.774-31A=
NM_016006.6:c.774-31A= MANE Select NP_057090.2:n.774-31A=