Canonical Allele Identifier: CA1310472108

Gene: PRKRA CHROMR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178436185A= , CM000664.2:g.178436185A=	GRCh38
NC_000002.11:g.179300912A= , CM000664.1:g.179300912A=	GRCh37
NC_000002.10:g.179009158A=	NCBI36
NG_009053.1:g.20047T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.744T= (PRKRA) MANE Select	ENSP00000318176.4:p.Ile248=
ENST00000448279.2:c.*472T= (PRKRA)	ENSP00000388455.1:n.*472T=
ENST00000457633.2:c.*248T= (PRKRA)	ENSP00000408668.2:n.*248T=
ENST00000474793.6:n.885T= (PRKRA)
ENST00000676505.1:c.*504T= (PRKRA)	ENSP00000504163.1:n.*504T=
ENST00000676586.1:n.2881T= (PRKRA)
ENST00000676752.1:n.2643T= (PRKRA)
ENST00000676832.1:c.*565T= (PRKRA)	ENSP00000503231.1:n.*565T=
ENST00000676922.1:c.*472T= (PRKRA)	ENSP00000503369.1:n.*472T=
ENST00000677136.1:n.2736T= (PRKRA)
ENST00000677206.1:c.*536T= (PRKRA)	ENSP00000503034.1:n.*536T=
ENST00000677253.1:c.*441T= (PRKRA)	ENSP00000503466.1:n.*441T=
ENST00000677386.1:c.*187T= (PRKRA)	ENSP00000503003.1:n.*187T=
ENST00000677460.1:c.*73T= (PRKRA)	ENSP00000504507.1:n.*73T=
ENST00000677584.1:c.*582T= (PRKRA)	ENSP00000504411.1:n.*582T=
ENST00000677689.1:c.489T= (PRKRA)	ENSP00000502919.1:p.Ile163=
ENST00000677859.1:c.597T= (PRKRA)
ENST00000677981.1:c.492T= (PRKRA)	ENSP00000503536.1:p.Ile164=
ENST00000678053.1:c.*504T= (PRKRA)	ENSP00000504330.1:n.*504T=
ENST00000678058.1:c.488T= (PRKRA)	ENSP00000503203.1:n.488T=
ENST00000678167.1:c.*298T= (PRKRA)	ENSP00000504479.1:n.*298T=
ENST00000678775.1:c.405T= (PRKRA)	ENSP00000504030.1:p.Ile135=
ENST00000678845.1:c.405T= (PRKRA)	ENSP00000503011.1:p.Ile135=
ENST00000679037.1:c.*412T= (PRKRA)	ENSP00000504421.1:n.*412T=
ENST00000679202.1:n.1831T= (PRKRA)
ENST00000325748.8:c.744T= (PRKRA)	ENSP00000318176.4:p.Ile248=
ENST00000424699.5:c.*536T= (PRKRA)	ENSP00000408029.1:n.*536T=
ENST00000432031.6:c.711T= (PRKRA)	ENSP00000393883.2:p.Ile237=
ENST00000487082.5:c.669T= (PRKRA)	ENSP00000430604.1:p.Ile223=
ENST00000490501.5:n.971T= (PRKRA)
NM_001139517.1:c.711T= (PRKRA)	NP_001132989.1:p.Ile237=
NM_001139518.1:c.669T= (PRKRA)	NP_001132990.1:p.Ile223=
NM_001316362.1:c.405T= (PRKRA)	NP_001303291.1:p.Ile135=
NM_003690.4:c.744T= (PRKRA)	NP_003681.1:p.Ile248=
NR_110204.1:n.966-2682A= (CHROMR)
XM_005246921.3:c.405T= (PRKRA)	XP_005246978.1:p.Ile135=
XM_011512063.1:c.489T= (PRKRA)	XP_011510365.1:p.Ile163=
XM_011512064.1:c.489T= (PRKRA)	XP_011510366.1:p.Ile163=
XM_011512066.1:c.405T= (PRKRA)	XP_011510368.1:p.Ile135=
XM_011512063.2:c.489T= (PRKRA)	XP_011510365.1:p.Ile163=
XM_011512066.2:c.405T= (PRKRA)	XP_011510368.1:p.Ile135=
XM_017005159.1:c.405T= (PRKRA)	XP_016860648.1:p.Ile135=
XR_001739008.2:n.785T= (PRKRA)
NM_003690.5:c.744T= (PRKRA) MANE Select	NP_003681.1:p.Ile248=
NM_001316362.2:c.405T= (PRKRA)	NP_001303291.1:p.Ile135=