Canonical Allele Identifier: CA1360918310
Gene: ABHD5 HGNC NCBI

Linked Data

dbSNP Id: rs2084820226
gnomAD v3: 3-43720411-A-T
gnomAD v4: 3-43720411-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.43720411A>T , CM000665.2:g.43720411A>T GRCh38
NC_000003.11:g.43761903A>T , CM000665.1:g.43761903A>T GRCh37
NC_000003.10:g.43736907A>T NCBI36
NG_007090.3:g.34529A>T
NG_007090.5:g.34542A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000454293.2:c.*29+1850A>T ENSP00000412014.2:n.*29+1850A>T
ENST00000463153.2:c.306+1850A>T
ENST00000643477.1:c.*2390A>T ENSP00000496220.1:n.*2390A>T
ENST00000644371.2:c.*1879A>T MANE Select ENSP00000495778.1:n.*1879A>T
ENST00000649763.1:c.*29+1850A>T ENSP00000497701.1:n.*29+1850A>T
ENST00000463153.1:n.309+1850A>T
NM_016006.4:c.*1879A>T NP_057090.2:n.*1879A>T
XM_011533779.1:c.*1879A>T XP_011532081.1:n.*1879A>T
XM_011533780.1:c.*1905A>T XP_011532082.1:n.*1905A>T
XR_940447.1:n.2874A>T
NM_001355186.1:c.*29+1850A>T NP_001342115.1:n.*29+1850A>T
NM_001365649.1:c.*1879A>T NP_001352578.1:n.*1879A>T
NM_001365650.1:c.*1905A>T NP_001352579.1:n.*1905A>T
NM_016006.5:c.*1879A>T NP_057090.2:n.*1879A>T
NR_158560.1:n.2940A>T
NM_001355186.2:c.*29+1850A>T NP_001342115.1:n.*29+1850A>T
NM_016006.6:c.*1879A>T MANE Select NP_057090.2:n.*1879A>T