Canonical Allele Identifier: CA8729457
Gene: PRKAR1A HGNC NCBI
FAM20A HGNC NCBI

Linked Data

ClinVar Variation Id: 536890
dbSNP Id: rs760033566

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68530328G>A , CM000679.2:g.68530328G>A GRCh38
NC_000017.10:g.66526469G>A , CM000679.1:g.66526469G>A GRCh37
NC_000017.9:g.64038064G>A NCBI36
NG_007093.3:g.121706G>A , LRG_514:g.121706G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000588188.7:c.973+327G>A (PRKAR1A) ENSP00000468106.2:n.973+327G>A
ENST00000711037.1:c.973+327G>A (PRKAR1A) ENSP00000518555.1:n.973+327G>A
ENST00000585427.6:c.1025G>A (PRKAR1A) ENSP00000464715.2:p.Arg342His
ENST00000585981.6:c.973+327G>A (PRKAR1A) ENSP00000467311.2:n.973+327G>A
ENST00000588178.6:c.1025G>A (PRKAR1A) ENSP00000465013.2:p.Arg342His
ENST00000589017.6:c.1025G>A (PRKAR1A) ENSP00000465445.2:p.Arg342His
ENST00000589480.6:c.1025G>A (PRKAR1A) ENSP00000466649.2:p.Arg342His
ENST00000592800.6:c.*250G>A (PRKAR1A) ENSP00000466314.2:n.*250G>A
ENST00000686019.1:n.2072G>A (PRKAR1A)
ENST00000689501.1:n.3217G>A (PRKAR1A)
ENST00000691392.1:n.1992G>A (PRKAR1A)
ENST00000589228.6:c.1025G>A (PRKAR1A) MANE Select ENSP00000464977.2:p.Arg342His
ENST00000358598.6:c.1025G>A (PRKAR1A) ENSP00000351410.1:p.Arg342His
ENST00000392710.8:c.*640G>A (PRKAR1A) ENSP00000376474.4:n.*640G>A
ENST00000392711.5:c.1025G>A (PRKAR1A) ENSP00000376475.1:p.Arg342His
ENST00000536854.6:c.1025G>A (PRKAR1A) ENSP00000445625.1:p.Arg342His
ENST00000586397.5:c.1025G>A (PRKAR1A) ENSP00000466459.1:p.Arg342His
ENST00000586541.5:c.437G>A (PRKAR1A)
ENST00000588188.6:c.973+327G>A (PRKAR1A) ENSP00000468106.2:n.973+327G>A
ENST00000589228.5:c.1025G>A (PRKAR1A) ENSP00000464977.1:p.Arg342His
ENST00000592800.5:c.710G>A (PRKAR1A)
NM_001276289.1:c.1025G>A (PRKAR1A) NP_001263218.1:p.Arg342His
NM_001276290.1:c.973+327G>A (PRKAR1A) NP_001263219.1:n.973+327G>A
NM_001278433.1:c.1025G>A (PRKAR1A) NP_001265362.1:p.Arg342His
NM_002734.4:c.1025G>A , LRG_514t1:c.1025G>A (PRKAR1A) NP_002725.1:p.Arg342His
NM_212471.2:c.1025G>A (PRKAR1A) NP_997636.1:p.Arg342His
NM_212472.2:c.1025G>A , LRG_514t2:c.1025G>A (PRKAR1A) NP_997637.1:p.Arg342His
XM_011524983.1:c.1025G>A (PRKAR1A) XP_011523285.1:p.Arg342His
XM_011524984.1:c.1025G>A (PRKAR1A) XP_011523286.1:p.Arg342His
XM_011524985.1:c.1025G>A (PRKAR1A) XP_011523287.1:p.Arg342His
XM_006721959.3:c.*7149C>T (FAM20A) XP_006722022.1:n.*7149C>T
XM_011524983.3:c.1025G>A (PRKAR1A) XP_011523285.1:p.Arg342His
XM_011524984.3:c.1025G>A (PRKAR1A) XP_011523286.1:p.Arg342His
XM_011524985.3:c.1025G>A (PRKAR1A) XP_011523287.1:p.Arg342His
XR_001752544.2:n.8871C>T (FAM20A)
XR_002958041.1:n.9023C>T (FAM20A)
NM_001369389.1:c.1025G>A (PRKAR1A) NP_001356318.1:p.Arg342His
NM_001369390.1:c.1025G>A (PRKAR1A) NP_001356319.1:p.Arg342His
NM_002734.5:c.1025G>A (PRKAR1A) MANE Select NP_002725.1:p.Arg342His
NM_001276289.2:c.1025G>A (PRKAR1A) NP_001263218.1:p.Arg342His
NM_001278433.2:c.1025G>A (PRKAR1A) NP_001265362.1:p.Arg342His
NM_212471.3:c.1025G>A (PRKAR1A) NP_997636.1:p.Arg342His