Canonical Allele Identifier: CA1047351989
Gene: ABHD5 HGNC NCBI

Linked Data

dbSNP Id: rs2084822185
gnomAD v3: 3-43720531-A-G
gnomAD v4: 3-43720531-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43720531A>G , CM000665.2:g.43720531A>G GRCh38
NC_000003.11:g.43762023A>G , CM000665.1:g.43762023A>G GRCh37
NC_000003.10:g.43737027A>G NCBI36
NG_007090.3:g.34649A>G
NG_007090.5:g.34662A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000454293.2:c.*29+1970A>G ENSP00000412014.2:n.*29+1970A>G
ENST00000463153.2:c.306+1970A>G
ENST00000643477.1:c.*2510A>G ENSP00000496220.1:n.*2510A>G
ENST00000644371.2:c.*1999A>G MANE Select ENSP00000495778.1:n.*1999A>G
ENST00000649763.1:c.*29+1970A>G ENSP00000497701.1:n.*29+1970A>G
ENST00000463153.1:n.309+1970A>G
NM_016006.4:c.*1999A>G NP_057090.2:n.*1999A>G
XM_011533779.1:c.*1999A>G XP_011532081.1:n.*1999A>G
XM_011533780.1:c.*2025A>G XP_011532082.1:n.*2025A>G
XR_940447.1:n.2994A>G
NM_001355186.1:c.*29+1970A>G NP_001342115.1:n.*29+1970A>G
NM_001365649.1:c.*1999A>G NP_001352578.1:n.*1999A>G
NM_001365650.1:c.*2025A>G NP_001352579.1:n.*2025A>G
NM_016006.5:c.*1999A>G NP_057090.2:n.*1999A>G
NR_158560.1:n.3060A>G
NM_001355186.2:c.*29+1970A>G NP_001342115.1:n.*29+1970A>G
NM_016006.6:c.*1999A>G MANE Select NP_057090.2:n.*1999A>G