Canonical Allele Identifier: CA1310471750
Gene: PRKRA HGNC NCBI
CHROMR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178432169G= , CM000664.2:g.178432169G= GRCh38
NC_000002.11:g.179296896G= , CM000664.1:g.179296896G= GRCh37
NC_000002.10:g.179005142G= NCBI36
NG_009053.1:g.24063C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325748.9:c.870C= (PRKRA) MANE Select ENSP00000318176.4:p.Ser290=
ENST00000448279.2:c.*598C= (PRKRA) ENSP00000388455.1:n.*598C=
ENST00000457633.2:c.*374C= (PRKRA) ENSP00000408668.2:n.*374C=
ENST00000474793.6:n.1011C= (PRKRA)
ENST00000676505.1:c.*630C= (PRKRA) ENSP00000504163.1:n.*630C=
ENST00000676586.1:n.3007C= (PRKRA)
ENST00000676752.1:n.2769C= (PRKRA)
ENST00000676832.1:c.*691C= (PRKRA) ENSP00000503231.1:n.*691C=
ENST00000676922.1:c.*598C= (PRKRA) ENSP00000503369.1:n.*598C=
ENST00000677136.1:n.2862C= (PRKRA)
ENST00000677206.1:c.*662C= (PRKRA) ENSP00000503034.1:n.*662C=
ENST00000677253.1:c.*567C= (PRKRA) ENSP00000503466.1:n.*567C=
ENST00000677386.1:c.*313C= (PRKRA) ENSP00000503003.1:n.*313C=
ENST00000677460.1:c.*199C= (PRKRA) ENSP00000504507.1:n.*199C=
ENST00000677584.1:c.*708C= (PRKRA) ENSP00000504411.1:n.*708C=
ENST00000677689.1:c.615C= (PRKRA) ENSP00000502919.1:p.Ser205=
ENST00000677859.1:c.723C= (PRKRA)
ENST00000677981.1:c.618C= (PRKRA) ENSP00000503536.1:p.Ser206=
ENST00000678053.1:c.*630C= (PRKRA) ENSP00000504330.1:n.*630C=
ENST00000678058.1:c.614C= (PRKRA) ENSP00000503203.1:n.614C=
ENST00000678167.1:c.*424C= (PRKRA) ENSP00000504479.1:n.*424C=
ENST00000678775.1:c.531C= (PRKRA) ENSP00000504030.1:p.Ser177=
ENST00000678845.1:c.531C= (PRKRA) ENSP00000503011.1:p.Ser177=
ENST00000679037.1:c.*538C= (PRKRA) ENSP00000504421.1:n.*538C=
ENST00000679202.1:n.1957C= (PRKRA)
ENST00000325748.8:c.870C= (PRKRA) ENSP00000318176.4:p.Ser290=
ENST00000424699.5:c.*662C= (PRKRA) ENSP00000408029.1:n.*662C=
ENST00000432031.6:c.837C= (PRKRA) ENSP00000393883.2:p.Ser279=
ENST00000487082.5:c.795C= (PRKRA) ENSP00000430604.1:p.Ser265=
ENST00000490501.5:n.1097C= (PRKRA)
NM_001139517.1:c.837C= (PRKRA) NP_001132989.1:p.Ser279=
NM_001139518.1:c.795C= (PRKRA) NP_001132990.1:p.Ser265=
NM_001316362.1:c.531C= (PRKRA) NP_001303291.1:p.Ser177=
NM_003690.4:c.870C= (PRKRA) NP_003681.1:p.Ser290=
NR_110204.1:n.872-1213G= (CHROMR)
NR_110205.1:n.716-1213G= (CHROMR)
NR_110206.1:n.651-1213G= (CHROMR)
XM_005246921.3:c.531C= (PRKRA) XP_005246978.1:p.Ser177=
XM_011512063.1:c.615C= (PRKRA) XP_011510365.1:p.Ser205=
XM_011512064.1:c.615C= (PRKRA) XP_011510366.1:p.Ser205=
XM_011512066.1:c.531C= (PRKRA) XP_011510368.1:p.Ser177=
XM_011512063.2:c.615C= (PRKRA) XP_011510365.1:p.Ser205=
XM_011512066.2:c.531C= (PRKRA) XP_011510368.1:p.Ser177=
XM_017005159.1:c.531C= (PRKRA) XP_016860648.1:p.Ser177=
XR_001739008.2:n.911C= (PRKRA)
NM_003690.5:c.870C= (PRKRA) MANE Select NP_003681.1:p.Ser290=
NM_001316362.2:c.531C= (PRKRA) NP_001303291.1:p.Ser177=