Canonical Allele Identifier: CA349399106

Gene: PRKRA CHROMR

Linked Data

• COSMIC: COSM1401540 ; COSM5130469
• MyVariant Identifiers: chr2:g.179296937A>T (hg19) ; chr2:g.178432210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432210A>T , CM000664.2:g.178432210A>T	GRCh38
NC_000002.11:g.179296937A>T , CM000664.1:g.179296937A>T	GRCh37
NC_000002.10:g.179005183A>T	NCBI36
NG_009053.1:g.24022T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.829T>A (PRKRA) MANE Select	ENSP00000318176.4:p.Ser277Thr
ENST00000448279.2:c.*557T>A (PRKRA)	ENSP00000388455.1:n.*557T>A
ENST00000457633.2:c.*333T>A (PRKRA)	ENSP00000408668.2:n.*333T>A
ENST00000474793.6:n.970T>A (PRKRA)
ENST00000676505.1:c.*589T>A (PRKRA)	ENSP00000504163.1:n.*589T>A
ENST00000676586.1:n.2966T>A (PRKRA)
ENST00000676752.1:n.2728T>A (PRKRA)
ENST00000676832.1:c.*650T>A (PRKRA)	ENSP00000503231.1:n.*650T>A
ENST00000676922.1:c.*557T>A (PRKRA)	ENSP00000503369.1:n.*557T>A
ENST00000677136.1:n.2821T>A (PRKRA)
ENST00000677206.1:c.*621T>A (PRKRA)	ENSP00000503034.1:n.*621T>A
ENST00000677253.1:c.*526T>A (PRKRA)	ENSP00000503466.1:n.*526T>A
ENST00000677386.1:c.*272T>A (PRKRA)	ENSP00000503003.1:n.*272T>A
ENST00000677460.1:c.*158T>A (PRKRA)	ENSP00000504507.1:n.*158T>A
ENST00000677584.1:c.*667T>A (PRKRA)	ENSP00000504411.1:n.*667T>A
ENST00000677689.1:c.574T>A (PRKRA)	ENSP00000502919.1:p.Ser192Thr
ENST00000677859.1:c.682T>A (PRKRA)
ENST00000677981.1:c.577T>A (PRKRA)	ENSP00000503536.1:p.Ser193Thr
ENST00000678053.1:c.*589T>A (PRKRA)	ENSP00000504330.1:n.*589T>A
ENST00000678058.1:c.573T>A (PRKRA)	ENSP00000503203.1:n.573T>A
ENST00000678167.1:c.*383T>A (PRKRA)	ENSP00000504479.1:n.*383T>A
ENST00000678775.1:c.490T>A (PRKRA)	ENSP00000504030.1:p.Ser164Thr
ENST00000678845.1:c.490T>A (PRKRA)	ENSP00000503011.1:p.Ser164Thr
ENST00000679037.1:c.*497T>A (PRKRA)	ENSP00000504421.1:n.*497T>A
ENST00000679202.1:n.1916T>A (PRKRA)
ENST00000325748.8:c.829T>A (PRKRA)	ENSP00000318176.4:p.Ser277Thr
ENST00000424699.5:c.*621T>A (PRKRA)	ENSP00000408029.1:n.*621T>A
ENST00000432031.6:c.796T>A (PRKRA)	ENSP00000393883.2:p.Ser266Thr
ENST00000487082.5:c.754T>A (PRKRA)	ENSP00000430604.1:p.Ser252Thr
ENST00000490501.5:n.1056T>A (PRKRA)
NM_001139517.1:c.796T>A (PRKRA)	NP_001132989.1:p.Ser266Thr
NM_001139518.1:c.754T>A (PRKRA)	NP_001132990.1:p.Ser252Thr
NM_001316362.1:c.490T>A (PRKRA)	NP_001303291.1:p.Ser164Thr
NM_003690.4:c.829T>A (PRKRA)	NP_003681.1:p.Ser277Thr
NR_110204.1:n.872-1172A>T (CHROMR)
NR_110205.1:n.716-1172A>T (CHROMR)
NR_110206.1:n.651-1172A>T (CHROMR)
XM_005246921.3:c.490T>A (PRKRA)	XP_005246978.1:p.Ser164Thr
XM_011512063.1:c.574T>A (PRKRA)	XP_011510365.1:p.Ser192Thr
XM_011512064.1:c.574T>A (PRKRA)	XP_011510366.1:p.Ser192Thr
XM_011512066.1:c.490T>A (PRKRA)	XP_011510368.1:p.Ser164Thr
XM_011512063.2:c.574T>A (PRKRA)	XP_011510365.1:p.Ser192Thr
XM_011512066.2:c.490T>A (PRKRA)	XP_011510368.1:p.Ser164Thr
XM_017005159.1:c.490T>A (PRKRA)	XP_016860648.1:p.Ser164Thr
XR_001739008.2:n.870T>A (PRKRA)
NM_003690.5:c.829T>A (PRKRA) MANE Select	NP_003681.1:p.Ser277Thr
NM_001316362.2:c.490T>A (PRKRA)	NP_001303291.1:p.Ser164Thr