Canonical Allele Identifier: CA408455835
Gene: ABHD12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.25307983T>G , CM000682.2:g.25307983T>G GRCh38
NC_000020.10:g.25288619T>G , CM000682.1:g.25288619T>G GRCh37
NC_000020.9:g.25236619T>G NCBI36
NG_028119.1:g.88000A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339157.10:c.850A>C MANE Select ENSP00000341408.5:p.Ser284Arg
ENST00000376542.8:c.850A>C ENSP00000365725.3:p.Ser284Arg
ENST00000465694.2:c.304A>C ENSP00000459278.2:p.Ser102Arg
ENST00000671784.1:c.304A>C ENSP00000500451.1:p.Ser102Arg
ENST00000671858.1:c.304A>C ENSP00000500550.1:p.Ser102Arg
ENST00000672001.1:n.361A>C
ENST00000672114.1:c.304A>C ENSP00000499945.1:p.Ser102Arg
ENST00000672258.1:c.304A>C ENSP00000499868.1:p.Ser102Arg
ENST00000672331.1:c.304A>C ENSP00000500286.1:p.Ser102Arg
ENST00000672358.1:c.304A>C ENSP00000500062.1:p.Ser102Arg
ENST00000672406.1:c.*189A>C ENSP00000500208.1:n.*189A>C
ENST00000672566.1:c.379A>C ENSP00000500106.1:p.Ser127Arg
ENST00000672596.1:c.304A>C ENSP00000500290.1:p.Ser102Arg
ENST00000672871.1:c.304A>C ENSP00000499949.1:p.Ser102Arg
ENST00000673094.1:c.304A>C ENSP00000500257.1:p.Ser102Arg
ENST00000673121.1:c.406A>C ENSP00000499839.1:p.Ser136Arg
ENST00000673227.1:c.304A>C ENSP00000500514.1:p.Ser102Arg
ENST00000673524.1:c.412A>C
ENST00000339157.9:c.850A>C ENSP00000341408.5:p.Ser284Arg
ENST00000376542.7:c.850A>C ENSP00000365725.3:p.Ser284Arg
ENST00000481556.1:n.504A>C
ENST00000491682.5:c.379A>C ENSP00000459495.1:p.Ser127Arg
ENST00000576316.5:c.154A>C ENSP00000459121.1:p.Ser52Arg
NM_001042472.2:c.850A>C NP_001035937.1:p.Ser284Arg
NM_015600.4:c.850A>C NP_056415.1:p.Ser284Arg
XM_005260698.1:c.850A>C XP_005260755.1:p.Ser284Arg
XM_005260699.3:c.850A>C XP_005260756.1:p.Ser284Arg
XM_005260700.1:c.379A>C XP_005260757.1:p.Ser127Arg
XM_011529214.1:c.850A>C XP_011527516.1:p.Ser284Arg
XM_011529215.1:c.379A>C XP_011527517.1:p.Ser127Arg
XM_011529216.1:c.379A>C XP_011527518.1:p.Ser127Arg
XM_011529217.1:c.193A>C XP_011527519.1:p.Ser65Arg
XM_011529218.1:c.193A>C XP_011527520.1:p.Ser65Arg
XM_011529214.2:c.850A>C XP_011527516.1:p.Ser284Arg
XM_017027796.1:c.379A>C XP_016883285.1:p.Ser127Arg
XR_002958465.1:n.860A>C
XR_002958466.1:n.980A>C
XR_002958467.1:n.539A>C
NM_001042472.3:c.850A>C MANE Select NP_001035937.1:p.Ser284Arg
NM_015600.5:c.850A>C NP_056415.1:p.Ser284Arg