Canonical Allele Identifier: CA1310471835

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432212A= , CM000664.2:g.178432212A=	GRCh38
NC_000002.11:g.179296939A= , CM000664.1:g.179296939A=	GRCh37
NC_000002.10:g.179005185A=	NCBI36
NG_009053.1:g.24020T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.827T= (PRKRA) MANE Select	ENSP00000318176.4:p.Leu276=
ENST00000448279.2:c.*555T= (PRKRA)	ENSP00000388455.1:n.*555T=
ENST00000457633.2:c.*331T= (PRKRA)	ENSP00000408668.2:n.*331T=
ENST00000474793.6:n.968T= (PRKRA)
ENST00000676505.1:c.*587T= (PRKRA)	ENSP00000504163.1:n.*587T=
ENST00000676586.1:n.2964T= (PRKRA)
ENST00000676752.1:n.2726T= (PRKRA)
ENST00000676832.1:c.*648T= (PRKRA)	ENSP00000503231.1:n.*648T=
ENST00000676922.1:c.*555T= (PRKRA)	ENSP00000503369.1:n.*555T=
ENST00000677136.1:n.2819T= (PRKRA)
ENST00000677206.1:c.*619T= (PRKRA)	ENSP00000503034.1:n.*619T=
ENST00000677253.1:c.*524T= (PRKRA)	ENSP00000503466.1:n.*524T=
ENST00000677386.1:c.*270T= (PRKRA)	ENSP00000503003.1:n.*270T=
ENST00000677460.1:c.*156T= (PRKRA)	ENSP00000504507.1:n.*156T=
ENST00000677584.1:c.*665T= (PRKRA)	ENSP00000504411.1:n.*665T=
ENST00000677689.1:c.572T= (PRKRA)	ENSP00000502919.1:p.Leu191=
ENST00000677859.1:c.680T= (PRKRA)
ENST00000677981.1:c.575T= (PRKRA)	ENSP00000503536.1:p.Leu192=
ENST00000678053.1:c.*587T= (PRKRA)	ENSP00000504330.1:n.*587T=
ENST00000678058.1:c.571T= (PRKRA)	ENSP00000503203.1:n.571T=
ENST00000678167.1:c.*381T= (PRKRA)	ENSP00000504479.1:n.*381T=
ENST00000678775.1:c.488T= (PRKRA)	ENSP00000504030.1:p.Leu163=
ENST00000678845.1:c.488T= (PRKRA)	ENSP00000503011.1:p.Leu163=
ENST00000679037.1:c.*495T= (PRKRA)	ENSP00000504421.1:n.*495T=
ENST00000679202.1:n.1914T= (PRKRA)
ENST00000325748.8:c.827T= (PRKRA)	ENSP00000318176.4:p.Leu276=
ENST00000424699.5:c.*619T= (PRKRA)	ENSP00000408029.1:n.*619T=
ENST00000432031.6:c.794T= (PRKRA)	ENSP00000393883.2:p.Leu265=
ENST00000487082.5:c.752T= (PRKRA)	ENSP00000430604.1:p.Leu251=
ENST00000490501.5:n.1054T= (PRKRA)
NM_001139517.1:c.794T= (PRKRA)	NP_001132989.1:p.Leu265=
NM_001139518.1:c.752T= (PRKRA)	NP_001132990.1:p.Leu251=
NM_001316362.1:c.488T= (PRKRA)	NP_001303291.1:p.Leu163=
NM_003690.4:c.827T= (PRKRA)	NP_003681.1:p.Leu276=
NR_110204.1:n.872-1170A= (CHROMR)
NR_110205.1:n.716-1170A= (CHROMR)
NR_110206.1:n.651-1170A= (CHROMR)
XM_005246921.3:c.488T= (PRKRA)	XP_005246978.1:p.Leu163=
XM_011512063.1:c.572T= (PRKRA)	XP_011510365.1:p.Leu191=
XM_011512064.1:c.572T= (PRKRA)	XP_011510366.1:p.Leu191=
XM_011512066.1:c.488T= (PRKRA)	XP_011510368.1:p.Leu163=
XM_011512063.2:c.572T= (PRKRA)	XP_011510365.1:p.Leu191=
XM_011512066.2:c.488T= (PRKRA)	XP_011510368.1:p.Leu163=
XM_017005159.1:c.488T= (PRKRA)	XP_016860648.1:p.Leu163=
XR_001739008.2:n.868T= (PRKRA)
NM_003690.5:c.827T= (PRKRA) MANE Select	NP_003681.1:p.Leu276=
NM_001316362.2:c.488T= (PRKRA)	NP_001303291.1:p.Leu163=