Canonical Allele Identifier: CA1047352137
Gene: ABHD5 HGNC NCBI

Linked Data

gnomAD v3: 3-43720890-C-T
gnomAD v4: 3-43720890-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43720890C>T , CM000665.2:g.43720890C>T GRCh38
NC_000003.11:g.43762382C>T , CM000665.1:g.43762382C>T GRCh37
NC_000003.10:g.43737386C>T NCBI36
NG_007090.3:g.35008C>T
NG_007090.5:g.35021C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000454293.2:c.*29+2329C>T ENSP00000412014.2:n.*29+2329C>T
ENST00000463153.2:c.306+2329C>T
ENST00000644371.2:c.*2358C>T MANE Select ENSP00000495778.1:n.*2358C>T
ENST00000649763.1:c.*29+2329C>T ENSP00000497701.1:n.*29+2329C>T
ENST00000463153.1:n.309+2329C>T
NM_016006.4:c.*2358C>T NP_057090.2:n.*2358C>T
XM_011533779.1:c.*2358C>T XP_011532081.1:n.*2358C>T
XM_011533780.1:c.*2384C>T XP_011532082.1:n.*2384C>T
XR_940447.1:n.3353C>T
NM_001355186.1:c.*29+2329C>T NP_001342115.1:n.*29+2329C>T
NM_001365649.1:c.*2358C>T NP_001352578.1:n.*2358C>T
NM_001365650.1:c.*2384C>T NP_001352579.1:n.*2384C>T
NM_016006.5:c.*2358C>T NP_057090.2:n.*2358C>T
NR_158560.1:n.3419C>T
NM_001355186.2:c.*29+2329C>T NP_001342115.1:n.*29+2329C>T
NM_016006.6:c.*2358C>T MANE Select NP_057090.2:n.*2358C>T