Canonical Allele Identifier: CA433377711
Gene: ABHD5 HGNC NCBI

Linked Data

dbSNP Id: rs2084511596
MyVariant Identifiers: chr3:g.43740837A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43699345A>G , CM000665.2:g.43699345A>G GRCh38
NC_000003.11:g.43740837A>G , CM000665.1:g.43740837A>G GRCh37
NC_000003.10:g.43715841A>G NCBI36
NG_007090.3:g.13463A>G
NG_007090.5:g.13476A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000013894.3:c.117A>G ENSP00000013894.2:p.Glu39=
ENST00000454293.2:c.-7A>G ENSP00000412014.2:n.-7A>G
ENST00000458276.7:c.117A>G ENSP00000390849.3:p.Glu39=
ENST00000642351.1:c.-7A>G ENSP00000494478.1:n.-7A>G
ENST00000643140.1:c.117A>G ENSP00000495588.1:p.Glu39=
ENST00000643477.1:c.117A>G ENSP00000496220.1:p.Glu39=
ENST00000643500.1:c.117A>G ENSP00000494735.1:p.Glu39=
ENST00000643520.1:n.165A>G
ENST00000644371.2:c.117A>G MANE Select ENSP00000495778.1:p.Glu39=
ENST00000646378.1:c.*167A>G ENSP00000495826.1:n.*167A>G
ENST00000646799.1:c.117A>G ENSP00000494829.1:p.Glu39=
ENST00000649763.1:c.117A>G ENSP00000497701.1:p.Glu39=
ENST00000013894.2:c.117A>G ENSP00000013894.2:p.Glu39=
ENST00000454293.1:c.-7A>G ENSP00000412014.1:n.-7A>G
ENST00000456453.5:c.-7A>G ENSP00000391582.1:n.-7A>G
ENST00000458276.6:c.117A>G ENSP00000390849.2:p.Glu39=
ENST00000486764.1:n.218A>G
NM_016006.4:c.117A>G NP_057090.2:p.Glu39=
XM_011533779.1:c.-7A>G XP_011532081.1:n.-7A>G
XM_011533780.1:c.117A>G XP_011532082.1:p.Glu39=
XR_940447.1:n.174A>G
NM_001355186.1:c.117A>G NP_001342115.1:p.Glu39=
NM_001365649.1:c.-7A>G NP_001352578.1:n.-7A>G
NM_001365650.1:c.117A>G NP_001352579.1:p.Glu39=
NM_016006.5:c.117A>G NP_057090.2:p.Glu39=
NR_158560.1:n.240A>G
NM_001355186.2:c.117A>G NP_001342115.1:p.Glu39=
NM_016006.6:c.117A>G MANE Select NP_057090.2:p.Glu39=