Canonical Allele Identifier: CA1310471905

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432252C= , CM000664.2:g.178432252C=	GRCh38
NC_000002.11:g.179296979C= , CM000664.1:g.179296979C=	GRCh37
NC_000002.10:g.179005225C=	NCBI36
NG_009053.1:g.23980G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.787G= (PRKRA) MANE Select	ENSP00000318176.4:p.Glu263=
ENST00000448279.2:c.*515G= (PRKRA)	ENSP00000388455.1:n.*515G=
ENST00000457633.2:c.*291G= (PRKRA)	ENSP00000408668.2:n.*291G=
ENST00000474793.6:n.928G= (PRKRA)
ENST00000676505.1:c.*547G= (PRKRA)	ENSP00000504163.1:n.*547G=
ENST00000676586.1:n.2924G= (PRKRA)
ENST00000676752.1:n.2686G= (PRKRA)
ENST00000676832.1:c.*608G= (PRKRA)	ENSP00000503231.1:n.*608G=
ENST00000676922.1:c.*515G= (PRKRA)	ENSP00000503369.1:n.*515G=
ENST00000677136.1:n.2779G= (PRKRA)
ENST00000677206.1:c.*579G= (PRKRA)	ENSP00000503034.1:n.*579G=
ENST00000677253.1:c.*484G= (PRKRA)	ENSP00000503466.1:n.*484G=
ENST00000677386.1:c.*230G= (PRKRA)	ENSP00000503003.1:n.*230G=
ENST00000677460.1:c.*116G= (PRKRA)	ENSP00000504507.1:n.*116G=
ENST00000677584.1:c.*625G= (PRKRA)	ENSP00000504411.1:n.*625G=
ENST00000677689.1:c.532G= (PRKRA)	ENSP00000502919.1:p.Glu178=
ENST00000677859.1:c.640G= (PRKRA)
ENST00000677981.1:c.535G= (PRKRA)	ENSP00000503536.1:p.Glu179=
ENST00000678053.1:c.*547G= (PRKRA)	ENSP00000504330.1:n.*547G=
ENST00000678058.1:c.531G= (PRKRA)	ENSP00000503203.1:n.531G=
ENST00000678167.1:c.*341G= (PRKRA)	ENSP00000504479.1:n.*341G=
ENST00000678775.1:c.448G= (PRKRA)	ENSP00000504030.1:p.Glu150=
ENST00000678845.1:c.448G= (PRKRA)	ENSP00000503011.1:p.Glu150=
ENST00000679037.1:c.*455G= (PRKRA)	ENSP00000504421.1:n.*455G=
ENST00000679202.1:n.1874G= (PRKRA)
ENST00000325748.8:c.787G= (PRKRA)	ENSP00000318176.4:p.Glu263=
ENST00000424699.5:c.*579G= (PRKRA)	ENSP00000408029.1:n.*579G=
ENST00000432031.6:c.754G= (PRKRA)	ENSP00000393883.2:p.Glu252=
ENST00000487082.5:c.712G= (PRKRA)	ENSP00000430604.1:p.Glu238=
ENST00000490501.5:n.1014G= (PRKRA)
NM_001139517.1:c.754G= (PRKRA)	NP_001132989.1:p.Glu252=
NM_001139518.1:c.712G= (PRKRA)	NP_001132990.1:p.Glu238=
NM_001316362.1:c.448G= (PRKRA)	NP_001303291.1:p.Glu150=
NM_003690.4:c.787G= (PRKRA)	NP_003681.1:p.Glu263=
NR_110204.1:n.872-1130C= (CHROMR)
NR_110205.1:n.716-1130C= (CHROMR)
NR_110206.1:n.651-1130C= (CHROMR)
XM_005246921.3:c.448G= (PRKRA)	XP_005246978.1:p.Glu150=
XM_011512063.1:c.532G= (PRKRA)	XP_011510365.1:p.Glu178=
XM_011512064.1:c.532G= (PRKRA)	XP_011510366.1:p.Glu178=
XM_011512066.1:c.448G= (PRKRA)	XP_011510368.1:p.Glu150=
XM_011512063.2:c.532G= (PRKRA)	XP_011510365.1:p.Glu178=
XM_011512066.2:c.448G= (PRKRA)	XP_011510368.1:p.Glu150=
XM_017005159.1:c.448G= (PRKRA)	XP_016860648.1:p.Glu150=
XR_001739008.2:n.828G= (PRKRA)
NM_003690.5:c.787G= (PRKRA) MANE Select	NP_003681.1:p.Glu263=
NM_001316362.2:c.448G= (PRKRA)	NP_001303291.1:p.Glu150=