Canonical Allele Identifier: CA352347434
Gene: ABHD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717688A>T , CM000665.2:g.43717688A>T GRCh38
NC_000003.11:g.43759180A>T , CM000665.1:g.43759180A>T GRCh37
NC_000003.10:g.43734184A>T NCBI36
NG_007090.3:g.31806A>T
NG_007090.5:g.31819A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000413300.2:c.268-78A>T
ENST00000454293.2:c.668A>T ENSP00000412014.2:p.Lys223Met
ENST00000458276.7:c.774-755A>T ENSP00000390849.3:n.774-755A>T
ENST00000463153.2:c.18A>T
ENST00000642351.1:c.668A>T ENSP00000494478.1:p.Lys223Met
ENST00000643140.1:c.*153A>T ENSP00000495588.1:n.*153A>T
ENST00000643477.1:c.*252A>T ENSP00000496220.1:n.*252A>T
ENST00000643500.1:c.679A>T ENSP00000494735.1:p.Arg227Ter
ENST00000643520.1:n.957A>T
ENST00000644371.2:c.791A>T MANE Select ENSP00000495778.1:p.Lys264Met
ENST00000646378.1:c.*841A>T ENSP00000495826.1:n.*841A>T
ENST00000646799.1:c.*248-755A>T ENSP00000494829.1:n.*248-755A>T
ENST00000649763.1:c.791A>T ENSP00000497701.1:p.Lys264Met
ENST00000413300.1:c.270-78A>T ENSP00000392159.1:n.270-78A>T
ENST00000458276.6:c.791A>T ENSP00000390849.2:p.Lys264Met
ENST00000463153.1:n.21A>T
NM_016006.4:c.791A>T NP_057090.2:p.Lys264Met
XM_011533779.1:c.668A>T XP_011532081.1:p.Lys223Met
XM_011533780.1:c.774-755A>T XP_011532082.1:n.774-755A>T
XR_940447.1:n.736A>T
NM_001355186.1:c.791A>T NP_001342115.1:p.Lys264Met
NM_001365649.1:c.668A>T NP_001352578.1:p.Lys223Met
NM_001365650.1:c.774-755A>T NP_001352579.1:n.774-755A>T
NM_016006.5:c.791A>T NP_057090.2:p.Lys264Met
NR_158560.1:n.802A>T
NM_001355186.2:c.791A>T NP_001342115.1:p.Lys264Met
NM_016006.6:c.791A>T MANE Select NP_057090.2:p.Lys264Met