Canonical Allele Identifier: CA1360917171
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717805A= , CM000665.2:g.43717805A= GRCh38
NC_000003.11:g.43759297A= , CM000665.1:g.43759297A= GRCh37
NC_000003.10:g.43734301A= NCBI36
NG_007090.3:g.31923A=
NG_007090.5:g.31936A=

Transcript Alleles

HGVS Amino-acid change
ENST00000413300.2:c.307A=
ENST00000454293.2:c.785A= ENSP00000412014.2:p.Asn262=
ENST00000458276.7:c.774-638A= ENSP00000390849.3:n.774-638A=
ENST00000463153.2:c.135A=
ENST00000642351.1:c.785A= ENSP00000494478.1:p.Asn262=
ENST00000643140.1:c.*270A= ENSP00000495588.1:n.*270A=
ENST00000643477.1:c.*369A= ENSP00000496220.1:n.*369A=
ENST00000643500.1:c.*109A= ENSP00000494735.1:n.*109A=
ENST00000643520.1:n.1074A=
ENST00000644371.2:c.908A= MANE Select ENSP00000495778.1:p.Asn303=
ENST00000646378.1:c.*958A= ENSP00000495826.1:n.*958A=
ENST00000646799.1:c.*248-638A= ENSP00000494829.1:n.*248-638A=
ENST00000649763.1:c.908A= ENSP00000497701.1:p.Asn303=
ENST00000413300.1:c.309A= ENSP00000392159.1:p.Gln103=
ENST00000458276.6:c.908A= ENSP00000390849.2:p.Asn303=
ENST00000463153.1:n.138A=
NM_016006.4:c.908A= NP_057090.2:p.Asn303=
XM_011533779.1:c.785A= XP_011532081.1:p.Asn262=
XM_011533780.1:c.774-638A= XP_011532082.1:n.774-638A=
XR_940447.1:n.853A=
NM_001355186.1:c.908A= NP_001342115.1:p.Asn303=
NM_001365649.1:c.785A= NP_001352578.1:p.Asn262=
NM_001365650.1:c.774-638A= NP_001352579.1:n.774-638A=
NM_016006.5:c.908A= NP_057090.2:p.Asn303=
NR_158560.1:n.919A=
NM_001355186.2:c.908A= NP_001342115.1:p.Asn303=
NM_016006.6:c.908A= MANE Select NP_057090.2:p.Asn303=