Canonical Allele Identifier: CA8729392
Gene: PRKAR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 502624
dbSNP Id: rs201774040

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68528898G>A , CM000679.2:g.68528898G>A GRCh38
NC_000017.10:g.66525039G>A , CM000679.1:g.66525039G>A GRCh37
NC_000017.9:g.64036634G>A NCBI36
NG_007093.3:g.120276G>A , LRG_514:g.120276G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000589228.6:c.798G>A MANE Select ENSP00000464977.2:p.Thr266=
ENST00000358598.6:c.798G>A ENSP00000351410.1:p.Thr266=
ENST00000392710.8:c.*413G>A ENSP00000376474.4:p.=
ENST00000392711.5:c.798G>A ENSP00000376475.1:p.Thr266=
ENST00000536854.6:c.798G>A ENSP00000445625.1:p.Thr266=
ENST00000585907.1:n.346G>A
ENST00000585981.5:c.798G>A ENSP00000467311.1:p.Thr266=
ENST00000586397.5:c.798G>A ENSP00000466459.1:p.Thr266=
ENST00000586541.5:n.210G>A
ENST00000588188.6:n.798G>A ENSP00000468106.2:p.Thr266=
ENST00000589228.5:c.798G>A ENSP00000464977.1:p.Thr266=
ENST00000592800.5:n.208G>A
NM_001276289.1:c.798G>A NP_001263218.1:p.Thr266=
NM_001276290.1:c.798G>A NP_001263219.1:p.Thr266=
NM_001278433.1:c.798G>A NP_001265362.1:p.Thr266=
NM_002734.4:c.798G>A , LRG_514t1:c.798G>A NP_002725.1:p.Thr266=
NM_212471.2:c.798G>A NP_997636.1:p.Thr266=
NM_212472.2:c.798G>A , LRG_514t2:c.798G>A NP_997637.1:p.Thr266=
XM_011524983.1:c.798G>A XP_011523285.1:p.Thr266=
XM_011524984.1:c.798G>A XP_011523286.1:p.Thr266=
XM_011524985.1:c.798G>A XP_011523287.1:p.Thr266=
XM_011524983.3:c.798G>A XP_011523285.1:p.Thr266=
XM_011524984.3:c.798G>A XP_011523286.1:p.Thr266=
XM_011524985.3:c.798G>A XP_011523287.1:p.Thr266=
NM_001369389.1:c.798G>A NP_001356318.1:p.Thr266=
NM_001369390.1:c.798G>A NP_001356319.1:p.Thr266=
NM_002734.5:c.798G>A MANE Select NP_002725.1:p.Thr266=
NM_001276289.2:c.798G>A NP_001263218.1:p.Thr266=
NM_001278433.2:c.798G>A NP_001265362.1:p.Thr266=
NM_212471.3:c.798G>A NP_997636.1:p.Thr266=