Linked Data
ClinVar Variation Id:
324796
dbSNP Id:
rs62087489
gnomAD v2:
17-66527349-C-T
gnomAD v3:
17-68531208-C-T
gnomAD v4:
17-68531208-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.68531208C>T , CM000679.2:g.68531208C>T | GRCh38 |
| NC_000017.10:g.66527349C>T , CM000679.1:g.66527349C>T | GRCh37 |
| NC_000017.9:g.64038944C>T | NCBI36 |
| NG_007093.3:g.122586C>T , LRG_514:g.122586C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000588188.7:c.973+1207C>T (PRKAR1A) | ENSP00000468106.2:n.973+1207C>T | |
| ENST00000711037.1:c.973+1207C>T (PRKAR1A) | ENSP00000518555.1:n.973+1207C>T | |
| ENST00000585427.6:c.*759C>T (PRKAR1A) | ENSP00000464715.2:n.*759C>T | |
| ENST00000585981.6:c.973+1207C>T (PRKAR1A) | ENSP00000467311.2:n.973+1207C>T | |
| ENST00000588178.6:c.*759C>T (PRKAR1A) | ENSP00000465013.2:n.*759C>T | |
| ENST00000589017.6:c.*759C>T (PRKAR1A) | ENSP00000465445.2:n.*759C>T | |
| ENST00000589480.6:c.*759C>T (PRKAR1A) | ENSP00000466649.2:n.*759C>T | |
| ENST00000592800.6:c.*1130C>T (PRKAR1A) | ENSP00000466314.2:n.*1130C>T | |
| ENST00000686019.1:n.2952C>T (PRKAR1A) | ||
| ENST00000689501.1:n.4097C>T (PRKAR1A) | ||
| ENST00000691392.1:n.2872C>T (PRKAR1A) | ||
| ENST00000589228.6:c.*759C>T (PRKAR1A) MANE Select | ENSP00000464977.2:n.*759C>T | |
| ENST00000358598.6:c.*759C>T (PRKAR1A) | ENSP00000351410.1:n.*759C>T | |
| ENST00000392710.8:c.*1520C>T (PRKAR1A) | ENSP00000376474.4:n.*1520C>T | |
| ENST00000392711.5:c.*759C>T (PRKAR1A) | ENSP00000376475.1:n.*759C>T | |
| ENST00000536854.6:c.*759C>T (PRKAR1A) | ENSP00000445625.1:n.*759C>T | |
| ENST00000588188.6:c.973+1207C>T (PRKAR1A) | ENSP00000468106.2:n.973+1207C>T | |
| ENST00000589228.5:c.*759C>T (PRKAR1A) | ENSP00000464977.1:n.*759C>T | |
| NM_001276289.1:c.*759C>T (PRKAR1A) | NP_001263218.1:n.*759C>T | |
| NM_001276290.1:c.973+1207C>T (PRKAR1A) | NP_001263219.1:n.973+1207C>T | |
| NM_001278433.1:c.*759C>T (PRKAR1A) | NP_001265362.1:n.*759C>T | |
| NM_002734.4:c.*759C>T , LRG_514t1:c.*759C>T (PRKAR1A) | NP_002725.1:n.*759C>T | |
| NM_212471.2:c.*759C>T (PRKAR1A) | NP_997636.1:n.*759C>T | |
| NM_212472.2:c.*759C>T , LRG_514t2:c.*759C>T (PRKAR1A) | NP_997637.1:n.*759C>T | |
| XM_011524983.1:c.*759C>T (PRKAR1A) | XP_011523285.1:n.*759C>T | |
| XM_011524984.1:c.*759C>T (PRKAR1A) | XP_011523286.1:n.*759C>T | |
| XM_011524985.1:c.*759C>T (PRKAR1A) | XP_011523287.1:n.*759C>T | |
| XM_006721959.3:c.*6269G>A (FAM20A) | XP_006722022.1:n.*6269G>A | |
| XM_011524983.3:c.*759C>T (PRKAR1A) | XP_011523285.1:n.*759C>T | |
| XM_011524984.3:c.*759C>T (PRKAR1A) | XP_011523286.1:n.*759C>T | |
| XM_011524985.3:c.*759C>T (PRKAR1A) | XP_011523287.1:n.*759C>T | |
| XR_001752544.2:n.7991G>A (FAM20A) | ||
| XR_002958041.1:n.8143G>A (FAM20A) | ||
| NM_001369389.1:c.*759C>T (PRKAR1A) | NP_001356318.1:n.*759C>T | |
| NM_001369390.1:c.*759C>T (PRKAR1A) | NP_001356319.1:n.*759C>T | |
| NM_002734.5:c.*759C>T (PRKAR1A) MANE Select | NP_002725.1:n.*759C>T | |
| NM_001276289.2:c.*759C>T (PRKAR1A) | NP_001263218.1:n.*759C>T | |
| NM_001278433.2:c.*759C>T (PRKAR1A) | NP_001265362.1:n.*759C>T | |
| NM_212471.3:c.*759C>T (PRKAR1A) | NP_997636.1:n.*759C>T |