Canonical Allele Identifier: CA1360907948
Gene: ABHD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43699461A= , CM000665.2:g.43699461A= GRCh38
NC_000003.11:g.43740953A= , CM000665.1:g.43740953A= GRCh37
NC_000003.10:g.43715957A= NCBI36
NG_007090.3:g.13579A=
NG_007090.5:g.13592A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013894.3:c.134-41A= ENSP00000013894.2:n.134-41A=
ENST00000454293.2:c.10+100A= ENSP00000412014.2:n.10+100A=
ENST00000458276.7:c.133+100A= ENSP00000390849.3:n.133+100A=
ENST00000642351.1:c.10+100A= ENSP00000494478.1:n.10+100A=
ENST00000643140.1:c.133+100A= ENSP00000495588.1:n.133+100A=
ENST00000643477.1:c.133+100A= ENSP00000496220.1:n.133+100A=
ENST00000643500.1:c.133+100A= ENSP00000494735.1:n.133+100A=
ENST00000643520.1:n.181+100A=
ENST00000644371.2:c.133+100A= MANE Select ENSP00000495778.1:n.133+100A=
ENST00000646378.1:c.*183+100A= ENSP00000495826.1:n.*183+100A=
ENST00000646799.1:c.133+100A= ENSP00000494829.1:n.133+100A=
ENST00000649763.1:c.133+100A= ENSP00000497701.1:n.133+100A=
ENST00000013894.2:c.134-41A= ENSP00000013894.2:n.134-41A=
ENST00000454293.1:c.10+100A= ENSP00000412014.1:n.10+100A=
ENST00000456453.5:c.10+100A= ENSP00000391582.1:n.10+100A=
ENST00000458276.6:c.133+100A= ENSP00000390849.2:n.133+100A=
ENST00000486764.1:n.334A=
NM_016006.4:c.133+100A= NP_057090.2:n.133+100A=
XM_011533779.1:c.10+100A= XP_011532081.1:n.10+100A=
XM_011533780.1:c.133+100A= XP_011532082.1:n.133+100A=
XR_940447.1:n.190+100A=
NM_001355186.1:c.133+100A= NP_001342115.1:n.133+100A=
NM_001365649.1:c.10+100A= NP_001352578.1:n.10+100A=
NM_001365650.1:c.133+100A= NP_001352579.1:n.133+100A=
NM_016006.5:c.133+100A= NP_057090.2:n.133+100A=
NR_158560.1:n.256+100A=
NM_001355186.2:c.133+100A= NP_001342115.1:n.133+100A=
NM_016006.6:c.133+100A= MANE Select NP_057090.2:n.133+100A=