Canonical Allele Identifier: CA1360917174
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717809T= , CM000665.2:g.43717809T= GRCh38
NC_000003.11:g.43759301T= , CM000665.1:g.43759301T= GRCh37
NC_000003.10:g.43734305T= NCBI36
NG_007090.3:g.31927T=
NG_007090.5:g.31940T=

Transcript Alleles

HGVS Amino-acid change
ENST00000413300.2:c.311T=
ENST00000454293.2:c.789T= ENSP00000412014.2:p.Ser263=
ENST00000458276.7:c.774-634T= ENSP00000390849.3:n.774-634T=
ENST00000463153.2:c.139T=
ENST00000642351.1:c.789T= ENSP00000494478.1:p.Ser263=
ENST00000643140.1:c.*274T= ENSP00000495588.1:n.*274T=
ENST00000643477.1:c.*373T= ENSP00000496220.1:n.*373T=
ENST00000643500.1:c.*113T= ENSP00000494735.1:n.*113T=
ENST00000643520.1:n.1078T=
ENST00000644371.2:c.912T= MANE Select ENSP00000495778.1:p.Ser304=
ENST00000646378.1:c.*962T= ENSP00000495826.1:n.*962T=
ENST00000646799.1:c.*248-634T= ENSP00000494829.1:n.*248-634T=
ENST00000649763.1:c.912T= ENSP00000497701.1:p.Ser304=
ENST00000413300.1:c.313T= ENSP00000392159.1:p.Trp105=
ENST00000458276.6:c.912T= ENSP00000390849.2:p.Ser304=
ENST00000463153.1:n.142T=
NM_016006.4:c.912T= NP_057090.2:p.Ser304=
XM_011533779.1:c.789T= XP_011532081.1:p.Ser263=
XM_011533780.1:c.774-634T= XP_011532082.1:n.774-634T=
XR_940447.1:n.857T=
NM_001355186.1:c.912T= NP_001342115.1:p.Ser304=
NM_001365649.1:c.789T= NP_001352578.1:p.Ser263=
NM_001365650.1:c.774-634T= NP_001352579.1:n.774-634T=
NM_016006.5:c.912T= NP_057090.2:p.Ser304=
NR_158560.1:n.923T=
NM_001355186.2:c.912T= NP_001342115.1:p.Ser304=
NM_016006.6:c.912T= MANE Select NP_057090.2:p.Ser304=