Canonical Allele Identifier: CA256533
Gene: PRKAR1A HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12674
dbSNP Id: rs137853303

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68522798C>T , CM000679.2:g.68522798C>T GRCh38
NC_000017.10:g.66518939C>T , CM000679.1:g.66518939C>T GRCh37
NC_000017.9:g.64030534C>T NCBI36
NG_007093.3:g.114176C>T , LRG_514:g.114176C>T

Transcript Alleles

HGVS Amino-acid change
NM_001276289.1:c.220C>T VV NP_001263218.1:p.Arg74Cys
NM_001276290.1:c.220C>T VV NP_001263219.1:p.Arg74Cys
NM_001278433.1:c.220C>T VV NP_001265362.1:p.Arg74Cys
NM_002734.4:c.220C>T , LRG_514t1:c.220C>T NP_002725.1:p.Arg74Cys
NM_212471.2:c.220C>T VV NP_997636.1:p.Arg74Cys
NM_212472.2:c.220C>T , LRG_514t2:c.220C>T NP_997637.1:p.Arg74Cys
XM_011524983.1:c.220C>T XP_011523285.1:p.Arg74Cys
XM_011524984.1:c.220C>T XP_011523286.1:p.Arg74Cys
XM_011524985.1:c.220C>T XP_011523287.1:p.Arg74Cys
XM_011524983.3:c.220C>T XP_011523285.1:p.Arg74Cys
XM_011524984.3:c.220C>T XP_011523286.1:p.Arg74Cys
XM_011524985.3:c.220C>T XP_011523287.1:p.Arg74Cys
ENST00000358598.6:c.220C>T ENSP00000351410.1:p.Arg74Cys
ENST00000392710.8:c.210C>T ENSP00000376474.4:p.Leu70=
ENST00000392711.5:c.220C>T ENSP00000376475.1:p.Arg74Cys
ENST00000536854.6:c.220C>T ENSP00000445625.1:p.Arg74Cys
ENST00000585427.5:c.220C>T ENSP00000464715.1:p.Arg74Cys
ENST00000585460.1:n.345C>T
ENST00000585608.5:c.220C>T ENSP00000466722.1:p.Arg74Cys
ENST00000585981.5:c.220C>T ENSP00000467311.1:p.Arg74Cys
ENST00000586397.5:c.220C>T ENSP00000466459.1:p.Arg74Cys
ENST00000588178.5:c.220C>T ENSP00000465013.1:p.Arg74Cys
ENST00000588188.6:n.220C>T ENSP00000468106.2:p.Arg74Cys
ENST00000588702.5:c.220C>T ENSP00000464701.1:p.Arg74Cys
ENST00000589017.5:c.220C>T ENSP00000465445.1:p.Arg74Cys
ENST00000589228.5:c.220C>T ENSP00000464977.1:p.Arg74Cys
ENST00000589480.5:c.220C>T ENSP00000466649.1:p.Arg74Cys