Canonical Allele Identifier: CA433377664
Gene: ABHD5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.43740771A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43699279A>T , CM000665.2:g.43699279A>T GRCh38
NC_000003.11:g.43740771A>T , CM000665.1:g.43740771A>T GRCh37
NC_000003.10:g.43715775A>T NCBI36
NG_007090.3:g.13397A>T
NG_007090.5:g.13410A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000013894.3:c.51A>T ENSP00000013894.2:p.Ser17=
ENST00000454293.2:c.-73A>T ENSP00000412014.2:n.-73A>T
ENST00000458276.7:c.51A>T ENSP00000390849.3:p.Ser17=
ENST00000642351.1:c.-73A>T ENSP00000494478.1:n.-73A>T
ENST00000643140.1:c.51A>T ENSP00000495588.1:p.Ser17=
ENST00000643477.1:c.51A>T ENSP00000496220.1:p.Ser17=
ENST00000643500.1:c.51A>T ENSP00000494735.1:p.Ser17=
ENST00000643520.1:n.99A>T
ENST00000644371.2:c.51A>T MANE Select ENSP00000495778.1:p.Ser17=
ENST00000646378.1:c.*101A>T ENSP00000495826.1:n.*101A>T
ENST00000646799.1:c.51A>T ENSP00000494829.1:p.Ser17=
ENST00000649763.1:c.51A>T ENSP00000497701.1:p.Ser17=
ENST00000013894.2:c.51A>T ENSP00000013894.2:p.Ser17=
ENST00000454293.1:c.-73A>T ENSP00000412014.1:n.-73A>T
ENST00000456453.5:c.-73A>T ENSP00000391582.1:n.-73A>T
ENST00000458276.6:c.51A>T ENSP00000390849.2:p.Ser17=
ENST00000486764.1:n.152A>T
NM_016006.4:c.51A>T NP_057090.2:p.Ser17=
XM_011533779.1:c.-73A>T XP_011532081.1:n.-73A>T
XM_011533780.1:c.51A>T XP_011532082.1:p.Ser17=
XR_940447.1:n.108A>T
NM_001355186.1:c.51A>T NP_001342115.1:p.Ser17=
NM_001365649.1:c.-73A>T NP_001352578.1:n.-73A>T
NM_001365650.1:c.51A>T NP_001352579.1:p.Ser17=
NM_016006.5:c.51A>T NP_057090.2:p.Ser17=
NR_158560.1:n.174A>T
NM_001355186.2:c.51A>T NP_001342115.1:p.Ser17=
NM_016006.6:c.51A>T MANE Select NP_057090.2:p.Ser17=