Canonical Allele Identifier: CA1310471776

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432179G= , CM000664.2:g.178432179G=	GRCh38
NC_000002.11:g.179296906G= , CM000664.1:g.179296906G=	GRCh37
NC_000002.10:g.179005152G=	NCBI36
NG_009053.1:g.24053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.860C= (PRKRA) MANE Select	ENSP00000318176.4:p.Ser287=
ENST00000448279.2:c.*588C= (PRKRA)	ENSP00000388455.1:n.*588C=
ENST00000457633.2:c.*364C= (PRKRA)	ENSP00000408668.2:n.*364C=
ENST00000474793.6:n.1001C= (PRKRA)
ENST00000676505.1:c.*620C= (PRKRA)	ENSP00000504163.1:n.*620C=
ENST00000676586.1:n.2997C= (PRKRA)
ENST00000676752.1:n.2759C= (PRKRA)
ENST00000676832.1:c.*681C= (PRKRA)	ENSP00000503231.1:n.*681C=
ENST00000676922.1:c.*588C= (PRKRA)	ENSP00000503369.1:n.*588C=
ENST00000677136.1:n.2852C= (PRKRA)
ENST00000677206.1:c.*652C= (PRKRA)	ENSP00000503034.1:n.*652C=
ENST00000677253.1:c.*557C= (PRKRA)	ENSP00000503466.1:n.*557C=
ENST00000677386.1:c.*303C= (PRKRA)	ENSP00000503003.1:n.*303C=
ENST00000677460.1:c.*189C= (PRKRA)	ENSP00000504507.1:n.*189C=
ENST00000677584.1:c.*698C= (PRKRA)	ENSP00000504411.1:n.*698C=
ENST00000677689.1:c.605C= (PRKRA)	ENSP00000502919.1:p.Ser202=
ENST00000677859.1:c.713C= (PRKRA)
ENST00000677981.1:c.608C= (PRKRA)	ENSP00000503536.1:p.Ser203=
ENST00000678053.1:c.*620C= (PRKRA)	ENSP00000504330.1:n.*620C=
ENST00000678058.1:c.604C= (PRKRA)	ENSP00000503203.1:n.604C=
ENST00000678167.1:c.*414C= (PRKRA)	ENSP00000504479.1:n.*414C=
ENST00000678775.1:c.521C= (PRKRA)	ENSP00000504030.1:p.Ser174=
ENST00000678845.1:c.521C= (PRKRA)	ENSP00000503011.1:p.Ser174=
ENST00000679037.1:c.*528C= (PRKRA)	ENSP00000504421.1:n.*528C=
ENST00000679202.1:n.1947C= (PRKRA)
ENST00000325748.8:c.860C= (PRKRA)	ENSP00000318176.4:p.Ser287=
ENST00000424699.5:c.*652C= (PRKRA)	ENSP00000408029.1:n.*652C=
ENST00000432031.6:c.827C= (PRKRA)	ENSP00000393883.2:p.Ser276=
ENST00000487082.5:c.785C= (PRKRA)	ENSP00000430604.1:p.Ser262=
ENST00000490501.5:n.1087C= (PRKRA)
NM_001139517.1:c.827C= (PRKRA)	NP_001132989.1:p.Ser276=
NM_001139518.1:c.785C= (PRKRA)	NP_001132990.1:p.Ser262=
NM_001316362.1:c.521C= (PRKRA)	NP_001303291.1:p.Ser174=
NM_003690.4:c.860C= (PRKRA)	NP_003681.1:p.Ser287=
NR_110204.1:n.872-1203G= (CHROMR)
NR_110205.1:n.716-1203G= (CHROMR)
NR_110206.1:n.651-1203G= (CHROMR)
XM_005246921.3:c.521C= (PRKRA)	XP_005246978.1:p.Ser174=
XM_011512063.1:c.605C= (PRKRA)	XP_011510365.1:p.Ser202=
XM_011512064.1:c.605C= (PRKRA)	XP_011510366.1:p.Ser202=
XM_011512066.1:c.521C= (PRKRA)	XP_011510368.1:p.Ser174=
XM_011512063.2:c.605C= (PRKRA)	XP_011510365.1:p.Ser202=
XM_011512066.2:c.521C= (PRKRA)	XP_011510368.1:p.Ser174=
XM_017005159.1:c.521C= (PRKRA)	XP_016860648.1:p.Ser174=
XR_001739008.2:n.901C= (PRKRA)
NM_003690.5:c.860C= (PRKRA) MANE Select	NP_003681.1:p.Ser287=
NM_001316362.2:c.521C= (PRKRA)	NP_001303291.1:p.Ser174=