Canonical Allele Identifier: CA1310471867

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432235T= , CM000664.2:g.178432235T=	GRCh38
NC_000002.11:g.179296962T= , CM000664.1:g.179296962T=	GRCh37
NC_000002.10:g.179005208T=	NCBI36
NG_009053.1:g.23997A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.804A= (PRKRA) MANE Select	ENSP00000318176.4:p.Gly268=
ENST00000448279.2:c.*532A= (PRKRA)	ENSP00000388455.1:n.*532A=
ENST00000457633.2:c.*308A= (PRKRA)	ENSP00000408668.2:n.*308A=
ENST00000474793.6:n.945A= (PRKRA)
ENST00000676505.1:c.*564A= (PRKRA)	ENSP00000504163.1:n.*564A=
ENST00000676586.1:n.2941A= (PRKRA)
ENST00000676752.1:n.2703A= (PRKRA)
ENST00000676832.1:c.*625A= (PRKRA)	ENSP00000503231.1:n.*625A=
ENST00000676922.1:c.*532A= (PRKRA)	ENSP00000503369.1:n.*532A=
ENST00000677136.1:n.2796A= (PRKRA)
ENST00000677206.1:c.*596A= (PRKRA)	ENSP00000503034.1:n.*596A=
ENST00000677253.1:c.*501A= (PRKRA)	ENSP00000503466.1:n.*501A=
ENST00000677386.1:c.*247A= (PRKRA)	ENSP00000503003.1:n.*247A=
ENST00000677460.1:c.*133A= (PRKRA)	ENSP00000504507.1:n.*133A=
ENST00000677584.1:c.*642A= (PRKRA)	ENSP00000504411.1:n.*642A=
ENST00000677689.1:c.549A= (PRKRA)	ENSP00000502919.1:p.Gly183=
ENST00000677859.1:c.657A= (PRKRA)
ENST00000677981.1:c.552A= (PRKRA)	ENSP00000503536.1:p.Gly184=
ENST00000678053.1:c.*564A= (PRKRA)	ENSP00000504330.1:n.*564A=
ENST00000678058.1:c.548A= (PRKRA)	ENSP00000503203.1:n.548A=
ENST00000678167.1:c.*358A= (PRKRA)	ENSP00000504479.1:n.*358A=
ENST00000678775.1:c.465A= (PRKRA)	ENSP00000504030.1:p.Gly155=
ENST00000678845.1:c.465A= (PRKRA)	ENSP00000503011.1:p.Gly155=
ENST00000679037.1:c.*472A= (PRKRA)	ENSP00000504421.1:n.*472A=
ENST00000679202.1:n.1891A= (PRKRA)
ENST00000325748.8:c.804A= (PRKRA)	ENSP00000318176.4:p.Gly268=
ENST00000424699.5:c.*596A= (PRKRA)	ENSP00000408029.1:n.*596A=
ENST00000432031.6:c.771A= (PRKRA)	ENSP00000393883.2:p.Gly257=
ENST00000487082.5:c.729A= (PRKRA)	ENSP00000430604.1:p.Gly243=
ENST00000490501.5:n.1031A= (PRKRA)
NM_001139517.1:c.771A= (PRKRA)	NP_001132989.1:p.Gly257=
NM_001139518.1:c.729A= (PRKRA)	NP_001132990.1:p.Gly243=
NM_001316362.1:c.465A= (PRKRA)	NP_001303291.1:p.Gly155=
NM_003690.4:c.804A= (PRKRA)	NP_003681.1:p.Gly268=
NR_110204.1:n.872-1147T= (CHROMR)
NR_110205.1:n.716-1147T= (CHROMR)
NR_110206.1:n.651-1147T= (CHROMR)
XM_005246921.3:c.465A= (PRKRA)	XP_005246978.1:p.Gly155=
XM_011512063.1:c.549A= (PRKRA)	XP_011510365.1:p.Gly183=
XM_011512064.1:c.549A= (PRKRA)	XP_011510366.1:p.Gly183=
XM_011512066.1:c.465A= (PRKRA)	XP_011510368.1:p.Gly155=
XM_011512063.2:c.549A= (PRKRA)	XP_011510365.1:p.Gly183=
XM_011512066.2:c.465A= (PRKRA)	XP_011510368.1:p.Gly155=
XM_017005159.1:c.465A= (PRKRA)	XP_016860648.1:p.Gly155=
XR_001739008.2:n.845A= (PRKRA)
NM_003690.5:c.804A= (PRKRA) MANE Select	NP_003681.1:p.Gly268=
NM_001316362.2:c.465A= (PRKRA)	NP_001303291.1:p.Gly155=