Canonical Allele Identifier: CA352344722
Gene: ABHD5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43699299T>C , CM000665.2:g.43699299T>C GRCh38
NC_000003.11:g.43740791T>C , CM000665.1:g.43740791T>C GRCh37
NC_000003.10:g.43715795T>C NCBI36
NG_007090.3:g.13417T>C
NG_007090.5:g.13430T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000013894.3:c.71T>C ENSP00000013894.2:p.Leu24Pro
ENST00000454293.2:c.-53T>C ENSP00000412014.2:n.-53T>C
ENST00000458276.7:c.71T>C ENSP00000390849.3:p.Leu24Pro
ENST00000642351.1:c.-53T>C ENSP00000494478.1:n.-53T>C
ENST00000643140.1:c.71T>C ENSP00000495588.1:p.Leu24Pro
ENST00000643477.1:c.71T>C ENSP00000496220.1:p.Leu24Pro
ENST00000643500.1:c.71T>C ENSP00000494735.1:p.Leu24Pro
ENST00000643520.1:n.119T>C
ENST00000644371.2:c.71T>C MANE Select ENSP00000495778.1:p.Leu24Pro
ENST00000646378.1:c.*121T>C ENSP00000495826.1:n.*121T>C
ENST00000646799.1:c.71T>C ENSP00000494829.1:p.Leu24Pro
ENST00000649763.1:c.71T>C ENSP00000497701.1:p.Leu24Pro
ENST00000013894.2:c.71T>C ENSP00000013894.2:p.Leu24Pro
ENST00000454293.1:c.-53T>C ENSP00000412014.1:n.-53T>C
ENST00000456453.5:c.-53T>C ENSP00000391582.1:n.-53T>C
ENST00000458276.6:c.71T>C ENSP00000390849.2:p.Leu24Pro
ENST00000486764.1:n.172T>C
NM_016006.4:c.71T>C NP_057090.2:p.Leu24Pro
XM_011533779.1:c.-53T>C XP_011532081.1:n.-53T>C
XM_011533780.1:c.71T>C XP_011532082.1:p.Leu24Pro
XR_940447.1:n.128T>C
NM_001355186.1:c.71T>C NP_001342115.1:p.Leu24Pro
NM_001365649.1:c.-53T>C NP_001352578.1:n.-53T>C
NM_001365650.1:c.71T>C NP_001352579.1:p.Leu24Pro
NM_016006.5:c.71T>C NP_057090.2:p.Leu24Pro
NR_158560.1:n.194T>C
NM_001355186.2:c.71T>C NP_001342115.1:p.Leu24Pro
NM_016006.6:c.71T>C MANE Select NP_057090.2:p.Leu24Pro