Canonical Allele Identifier: CA1310471861

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432231A= , CM000664.2:g.178432231A=	GRCh38
NC_000002.11:g.179296958A= , CM000664.1:g.179296958A=	GRCh37
NC_000002.10:g.179005204A=	NCBI36
NG_009053.1:g.24001T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.808T= (PRKRA) MANE Select	ENSP00000318176.4:p.Tyr270=
ENST00000448279.2:c.*536T= (PRKRA)	ENSP00000388455.1:n.*536T=
ENST00000457633.2:c.*312T= (PRKRA)	ENSP00000408668.2:n.*312T=
ENST00000474793.6:n.949T= (PRKRA)
ENST00000676505.1:c.*568T= (PRKRA)	ENSP00000504163.1:n.*568T=
ENST00000676586.1:n.2945T= (PRKRA)
ENST00000676752.1:n.2707T= (PRKRA)
ENST00000676832.1:c.*629T= (PRKRA)	ENSP00000503231.1:n.*629T=
ENST00000676922.1:c.*536T= (PRKRA)	ENSP00000503369.1:n.*536T=
ENST00000677136.1:n.2800T= (PRKRA)
ENST00000677206.1:c.*600T= (PRKRA)	ENSP00000503034.1:n.*600T=
ENST00000677253.1:c.*505T= (PRKRA)	ENSP00000503466.1:n.*505T=
ENST00000677386.1:c.*251T= (PRKRA)	ENSP00000503003.1:n.*251T=
ENST00000677460.1:c.*137T= (PRKRA)	ENSP00000504507.1:n.*137T=
ENST00000677584.1:c.*646T= (PRKRA)	ENSP00000504411.1:n.*646T=
ENST00000677689.1:c.553T= (PRKRA)	ENSP00000502919.1:p.Tyr185=
ENST00000677859.1:c.661T= (PRKRA)
ENST00000677981.1:c.556T= (PRKRA)	ENSP00000503536.1:p.Tyr186=
ENST00000678053.1:c.*568T= (PRKRA)	ENSP00000504330.1:n.*568T=
ENST00000678058.1:c.552T= (PRKRA)	ENSP00000503203.1:n.552T=
ENST00000678167.1:c.*362T= (PRKRA)	ENSP00000504479.1:n.*362T=
ENST00000678775.1:c.469T= (PRKRA)	ENSP00000504030.1:p.Tyr157=
ENST00000678845.1:c.469T= (PRKRA)	ENSP00000503011.1:p.Tyr157=
ENST00000679037.1:c.*476T= (PRKRA)	ENSP00000504421.1:n.*476T=
ENST00000679202.1:n.1895T= (PRKRA)
ENST00000325748.8:c.808T= (PRKRA)	ENSP00000318176.4:p.Tyr270=
ENST00000424699.5:c.*600T= (PRKRA)	ENSP00000408029.1:n.*600T=
ENST00000432031.6:c.775T= (PRKRA)	ENSP00000393883.2:p.Tyr259=
ENST00000487082.5:c.733T= (PRKRA)	ENSP00000430604.1:p.Tyr245=
ENST00000490501.5:n.1035T= (PRKRA)
NM_001139517.1:c.775T= (PRKRA)	NP_001132989.1:p.Tyr259=
NM_001139518.1:c.733T= (PRKRA)	NP_001132990.1:p.Tyr245=
NM_001316362.1:c.469T= (PRKRA)	NP_001303291.1:p.Tyr157=
NM_003690.4:c.808T= (PRKRA)	NP_003681.1:p.Tyr270=
NR_110204.1:n.872-1151A= (CHROMR)
NR_110205.1:n.716-1151A= (CHROMR)
NR_110206.1:n.651-1151A= (CHROMR)
XM_005246921.3:c.469T= (PRKRA)	XP_005246978.1:p.Tyr157=
XM_011512063.1:c.553T= (PRKRA)	XP_011510365.1:p.Tyr185=
XM_011512064.1:c.553T= (PRKRA)	XP_011510366.1:p.Tyr185=
XM_011512066.1:c.469T= (PRKRA)	XP_011510368.1:p.Tyr157=
XM_011512063.2:c.553T= (PRKRA)	XP_011510365.1:p.Tyr185=
XM_011512066.2:c.469T= (PRKRA)	XP_011510368.1:p.Tyr157=
XM_017005159.1:c.469T= (PRKRA)	XP_016860648.1:p.Tyr157=
XR_001739008.2:n.849T= (PRKRA)
NM_003690.5:c.808T= (PRKRA) MANE Select	NP_003681.1:p.Tyr270=
NM_001316362.2:c.469T= (PRKRA)	NP_001303291.1:p.Tyr157=