Canonical Allele Identifier: CA1310471885

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432243C= , CM000664.2:g.178432243C=	GRCh38
NC_000002.11:g.179296970C= , CM000664.1:g.179296970C=	GRCh37
NC_000002.10:g.179005216C=	NCBI36
NG_009053.1:g.23989G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.796G= (PRKRA) MANE Select	ENSP00000318176.4:p.Ala266=
ENST00000448279.2:c.*524G= (PRKRA)	ENSP00000388455.1:n.*524G=
ENST00000457633.2:c.*300G= (PRKRA)	ENSP00000408668.2:n.*300G=
ENST00000474793.6:n.937G= (PRKRA)
ENST00000676505.1:c.*556G= (PRKRA)	ENSP00000504163.1:n.*556G=
ENST00000676586.1:n.2933G= (PRKRA)
ENST00000676752.1:n.2695G= (PRKRA)
ENST00000676832.1:c.*617G= (PRKRA)	ENSP00000503231.1:n.*617G=
ENST00000676922.1:c.*524G= (PRKRA)	ENSP00000503369.1:n.*524G=
ENST00000677136.1:n.2788G= (PRKRA)
ENST00000677206.1:c.*588G= (PRKRA)	ENSP00000503034.1:n.*588G=
ENST00000677253.1:c.*493G= (PRKRA)	ENSP00000503466.1:n.*493G=
ENST00000677386.1:c.*239G= (PRKRA)	ENSP00000503003.1:n.*239G=
ENST00000677460.1:c.*125G= (PRKRA)	ENSP00000504507.1:n.*125G=
ENST00000677584.1:c.*634G= (PRKRA)	ENSP00000504411.1:n.*634G=
ENST00000677689.1:c.541G= (PRKRA)	ENSP00000502919.1:p.Ala181=
ENST00000677859.1:c.649G= (PRKRA)
ENST00000677981.1:c.544G= (PRKRA)	ENSP00000503536.1:p.Ala182=
ENST00000678053.1:c.*556G= (PRKRA)	ENSP00000504330.1:n.*556G=
ENST00000678058.1:c.540G= (PRKRA)	ENSP00000503203.1:n.540G=
ENST00000678167.1:c.*350G= (PRKRA)	ENSP00000504479.1:n.*350G=
ENST00000678775.1:c.457G= (PRKRA)	ENSP00000504030.1:p.Ala153=
ENST00000678845.1:c.457G= (PRKRA)	ENSP00000503011.1:p.Ala153=
ENST00000679037.1:c.*464G= (PRKRA)	ENSP00000504421.1:n.*464G=
ENST00000679202.1:n.1883G= (PRKRA)
ENST00000325748.8:c.796G= (PRKRA)	ENSP00000318176.4:p.Ala266=
ENST00000424699.5:c.*588G= (PRKRA)	ENSP00000408029.1:n.*588G=
ENST00000432031.6:c.763G= (PRKRA)	ENSP00000393883.2:p.Ala255=
ENST00000487082.5:c.721G= (PRKRA)	ENSP00000430604.1:p.Ala241=
ENST00000490501.5:n.1023G= (PRKRA)
NM_001139517.1:c.763G= (PRKRA)	NP_001132989.1:p.Ala255=
NM_001139518.1:c.721G= (PRKRA)	NP_001132990.1:p.Ala241=
NM_001316362.1:c.457G= (PRKRA)	NP_001303291.1:p.Ala153=
NM_003690.4:c.796G= (PRKRA)	NP_003681.1:p.Ala266=
NR_110204.1:n.872-1139C= (CHROMR)
NR_110205.1:n.716-1139C= (CHROMR)
NR_110206.1:n.651-1139C= (CHROMR)
XM_005246921.3:c.457G= (PRKRA)	XP_005246978.1:p.Ala153=
XM_011512063.1:c.541G= (PRKRA)	XP_011510365.1:p.Ala181=
XM_011512064.1:c.541G= (PRKRA)	XP_011510366.1:p.Ala181=
XM_011512066.1:c.457G= (PRKRA)	XP_011510368.1:p.Ala153=
XM_011512063.2:c.541G= (PRKRA)	XP_011510365.1:p.Ala181=
XM_011512066.2:c.457G= (PRKRA)	XP_011510368.1:p.Ala153=
XM_017005159.1:c.457G= (PRKRA)	XP_016860648.1:p.Ala153=
XR_001739008.2:n.837G= (PRKRA)
NM_003690.5:c.796G= (PRKRA) MANE Select	NP_003681.1:p.Ala266=
NM_001316362.2:c.457G= (PRKRA)	NP_001303291.1:p.Ala153=