Canonical Allele Identifier: CA349398822
Gene: PRKRA HGNC NCBI
CHROMR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178432177C>G , CM000664.2:g.178432177C>G GRCh38
NC_000002.11:g.179296904C>G , CM000664.1:g.179296904C>G GRCh37
NC_000002.10:g.179005150C>G NCBI36
NG_009053.1:g.24055G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000325748.9:c.862G>C (PRKRA) MANE Select ENSP00000318176.4:p.Gly288Arg
ENST00000448279.2:c.*590G>C (PRKRA) ENSP00000388455.1:n.*590G>C
ENST00000457633.2:c.*366G>C (PRKRA) ENSP00000408668.2:n.*366G>C
ENST00000474793.6:n.1003G>C (PRKRA)
ENST00000676505.1:c.*622G>C (PRKRA) ENSP00000504163.1:n.*622G>C
ENST00000676586.1:n.2999G>C (PRKRA)
ENST00000676752.1:n.2761G>C (PRKRA)
ENST00000676832.1:c.*683G>C (PRKRA) ENSP00000503231.1:n.*683G>C
ENST00000676922.1:c.*590G>C (PRKRA) ENSP00000503369.1:n.*590G>C
ENST00000677136.1:n.2854G>C (PRKRA)
ENST00000677206.1:c.*654G>C (PRKRA) ENSP00000503034.1:n.*654G>C
ENST00000677253.1:c.*559G>C (PRKRA) ENSP00000503466.1:n.*559G>C
ENST00000677386.1:c.*305G>C (PRKRA) ENSP00000503003.1:n.*305G>C
ENST00000677460.1:c.*191G>C (PRKRA) ENSP00000504507.1:n.*191G>C
ENST00000677584.1:c.*700G>C (PRKRA) ENSP00000504411.1:n.*700G>C
ENST00000677689.1:c.607G>C (PRKRA) ENSP00000502919.1:p.Gly203Arg
ENST00000677859.1:c.715G>C (PRKRA)
ENST00000677981.1:c.610G>C (PRKRA) ENSP00000503536.1:p.Gly204Arg
ENST00000678053.1:c.*622G>C (PRKRA) ENSP00000504330.1:n.*622G>C
ENST00000678058.1:c.606G>C (PRKRA) ENSP00000503203.1:n.606G>C
ENST00000678167.1:c.*416G>C (PRKRA) ENSP00000504479.1:n.*416G>C
ENST00000678775.1:c.523G>C (PRKRA) ENSP00000504030.1:p.Gly175Arg
ENST00000678845.1:c.523G>C (PRKRA) ENSP00000503011.1:p.Gly175Arg
ENST00000679037.1:c.*530G>C (PRKRA) ENSP00000504421.1:n.*530G>C
ENST00000679202.1:n.1949G>C (PRKRA)
ENST00000325748.8:c.862G>C (PRKRA) ENSP00000318176.4:p.Gly288Arg
ENST00000424699.5:c.*654G>C (PRKRA) ENSP00000408029.1:n.*654G>C
ENST00000432031.6:c.829G>C (PRKRA) ENSP00000393883.2:p.Gly277Arg
ENST00000487082.5:c.787G>C (PRKRA) ENSP00000430604.1:p.Gly263Arg
ENST00000490501.5:n.1089G>C (PRKRA)
NM_001139517.1:c.829G>C (PRKRA) NP_001132989.1:p.Gly277Arg
NM_001139518.1:c.787G>C (PRKRA) NP_001132990.1:p.Gly263Arg
NM_001316362.1:c.523G>C (PRKRA) NP_001303291.1:p.Gly175Arg
NM_003690.4:c.862G>C (PRKRA) NP_003681.1:p.Gly288Arg
NR_110204.1:n.872-1205C>G (CHROMR)
NR_110205.1:n.716-1205C>G (CHROMR)
NR_110206.1:n.651-1205C>G (CHROMR)
XM_005246921.3:c.523G>C (PRKRA) XP_005246978.1:p.Gly175Arg
XM_011512063.1:c.607G>C (PRKRA) XP_011510365.1:p.Gly203Arg
XM_011512064.1:c.607G>C (PRKRA) XP_011510366.1:p.Gly203Arg
XM_011512066.1:c.523G>C (PRKRA) XP_011510368.1:p.Gly175Arg
XM_011512063.2:c.607G>C (PRKRA) XP_011510365.1:p.Gly203Arg
XM_011512066.2:c.523G>C (PRKRA) XP_011510368.1:p.Gly175Arg
XM_017005159.1:c.523G>C (PRKRA) XP_016860648.1:p.Gly175Arg
XR_001739008.2:n.903G>C (PRKRA)
NM_003690.5:c.862G>C (PRKRA) MANE Select NP_003681.1:p.Gly288Arg
NM_001316362.2:c.523G>C (PRKRA) NP_001303291.1:p.Gly175Arg