Canonical Allele Identifier: CA352347620
Gene: ABHD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43717770A>G , CM000665.2:g.43717770A>G GRCh38
NC_000003.11:g.43759262A>G , CM000665.1:g.43759262A>G GRCh37
NC_000003.10:g.43734266A>G NCBI36
NG_007090.3:g.31888A>G
NG_007090.5:g.31901A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000413300.2:c.272A>G
ENST00000454293.2:c.750A>G ENSP00000412014.2:p.Ser250=
ENST00000458276.7:c.774-673A>G ENSP00000390849.3:n.774-673A>G
ENST00000463153.2:c.100A>G
ENST00000642351.1:c.750A>G ENSP00000494478.1:p.Ser250=
ENST00000643140.1:c.*235A>G ENSP00000495588.1:n.*235A>G
ENST00000643477.1:c.*334A>G ENSP00000496220.1:n.*334A>G
ENST00000643500.1:c.*74A>G ENSP00000494735.1:n.*74A>G
ENST00000643520.1:n.1039A>G
ENST00000644371.2:c.873A>G MANE Select ENSP00000495778.1:p.Ser291=
ENST00000646378.1:c.*923A>G ENSP00000495826.1:n.*923A>G
ENST00000646799.1:c.*248-673A>G ENSP00000494829.1:n.*248-673A>G
ENST00000649763.1:c.873A>G ENSP00000497701.1:p.Ser291=
ENST00000413300.1:c.274A>G ENSP00000392159.1:p.Ser92Gly
ENST00000458276.6:c.873A>G ENSP00000390849.2:p.Ser291=
ENST00000463153.1:n.103A>G
NM_016006.4:c.873A>G NP_057090.2:p.Ser291=
XM_011533779.1:c.750A>G XP_011532081.1:p.Ser250=
XM_011533780.1:c.774-673A>G XP_011532082.1:n.774-673A>G
XR_940447.1:n.818A>G
NM_001355186.1:c.873A>G NP_001342115.1:p.Ser291=
NM_001365649.1:c.750A>G NP_001352578.1:p.Ser250=
NM_001365650.1:c.774-673A>G NP_001352579.1:n.774-673A>G
NM_016006.5:c.873A>G NP_057090.2:p.Ser291=
NR_158560.1:n.884A>G
NM_001355186.2:c.873A>G NP_001342115.1:p.Ser291=
NM_016006.6:c.873A>G MANE Select NP_057090.2:p.Ser291=