Canonical Allele Identifier: CA349399074

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296934T>C (hg19) ; chr2:g.178432207T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432207T>C , CM000664.2:g.178432207T>C	GRCh38
NC_000002.11:g.179296934T>C , CM000664.1:g.179296934T>C	GRCh37
NC_000002.10:g.179005180T>C	NCBI36
NG_009053.1:g.24025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.832A>G (PRKRA) MANE Select	ENSP00000318176.4:p.Thr278Ala
ENST00000448279.2:c.*560A>G (PRKRA)	ENSP00000388455.1:n.*560A>G
ENST00000457633.2:c.*336A>G (PRKRA)	ENSP00000408668.2:n.*336A>G
ENST00000474793.6:n.973A>G (PRKRA)
ENST00000676505.1:c.*592A>G (PRKRA)	ENSP00000504163.1:n.*592A>G
ENST00000676586.1:n.2969A>G (PRKRA)
ENST00000676752.1:n.2731A>G (PRKRA)
ENST00000676832.1:c.*653A>G (PRKRA)	ENSP00000503231.1:n.*653A>G
ENST00000676922.1:c.*560A>G (PRKRA)	ENSP00000503369.1:n.*560A>G
ENST00000677136.1:n.2824A>G (PRKRA)
ENST00000677206.1:c.*624A>G (PRKRA)	ENSP00000503034.1:n.*624A>G
ENST00000677253.1:c.*529A>G (PRKRA)	ENSP00000503466.1:n.*529A>G
ENST00000677386.1:c.*275A>G (PRKRA)	ENSP00000503003.1:n.*275A>G
ENST00000677460.1:c.*161A>G (PRKRA)	ENSP00000504507.1:n.*161A>G
ENST00000677584.1:c.*670A>G (PRKRA)	ENSP00000504411.1:n.*670A>G
ENST00000677689.1:c.577A>G (PRKRA)	ENSP00000502919.1:p.Thr193Ala
ENST00000677859.1:c.685A>G (PRKRA)
ENST00000677981.1:c.580A>G (PRKRA)	ENSP00000503536.1:p.Thr194Ala
ENST00000678053.1:c.*592A>G (PRKRA)	ENSP00000504330.1:n.*592A>G
ENST00000678058.1:c.576A>G (PRKRA)	ENSP00000503203.1:n.576A>G
ENST00000678167.1:c.*386A>G (PRKRA)	ENSP00000504479.1:n.*386A>G
ENST00000678775.1:c.493A>G (PRKRA)	ENSP00000504030.1:p.Thr165Ala
ENST00000678845.1:c.493A>G (PRKRA)	ENSP00000503011.1:p.Thr165Ala
ENST00000679037.1:c.*500A>G (PRKRA)	ENSP00000504421.1:n.*500A>G
ENST00000679202.1:n.1919A>G (PRKRA)
ENST00000325748.8:c.832A>G (PRKRA)	ENSP00000318176.4:p.Thr278Ala
ENST00000424699.5:c.*624A>G (PRKRA)	ENSP00000408029.1:n.*624A>G
ENST00000432031.6:c.799A>G (PRKRA)	ENSP00000393883.2:p.Thr267Ala
ENST00000487082.5:c.757A>G (PRKRA)	ENSP00000430604.1:p.Thr253Ala
ENST00000490501.5:n.1059A>G (PRKRA)
NM_001139517.1:c.799A>G (PRKRA)	NP_001132989.1:p.Thr267Ala
NM_001139518.1:c.757A>G (PRKRA)	NP_001132990.1:p.Thr253Ala
NM_001316362.1:c.493A>G (PRKRA)	NP_001303291.1:p.Thr165Ala
NM_003690.4:c.832A>G (PRKRA)	NP_003681.1:p.Thr278Ala
NR_110204.1:n.872-1175T>C (CHROMR)
NR_110205.1:n.716-1175T>C (CHROMR)
NR_110206.1:n.651-1175T>C (CHROMR)
XM_005246921.3:c.493A>G (PRKRA)	XP_005246978.1:p.Thr165Ala
XM_011512063.1:c.577A>G (PRKRA)	XP_011510365.1:p.Thr193Ala
XM_011512064.1:c.577A>G (PRKRA)	XP_011510366.1:p.Thr193Ala
XM_011512066.1:c.493A>G (PRKRA)	XP_011510368.1:p.Thr165Ala
XM_011512063.2:c.577A>G (PRKRA)	XP_011510365.1:p.Thr193Ala
XM_011512066.2:c.493A>G (PRKRA)	XP_011510368.1:p.Thr165Ala
XM_017005159.1:c.493A>G (PRKRA)	XP_016860648.1:p.Thr165Ala
XR_001739008.2:n.873A>G (PRKRA)
NM_003690.5:c.832A>G (PRKRA) MANE Select	NP_003681.1:p.Thr278Ala
NM_001316362.2:c.493A>G (PRKRA)	NP_001303291.1:p.Thr165Ala