Canonical Allele Identifier: CA349398696

Gene: PRKRA CHROMR

Linked Data

• MyVariant Identifiers: chr2:g.179296887A>T (hg19) ; chr2:g.178432160A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178432160A>T , CM000664.2:g.178432160A>T	GRCh38
NC_000002.11:g.179296887A>T , CM000664.1:g.179296887A>T	GRCh37
NC_000002.10:g.179005133A>T	NCBI36
NG_009053.1:g.24072T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325748.9:c.879T>A (PRKRA) MANE Select	ENSP00000318176.4:p.Asn293Lys
ENST00000448279.2:c.*607T>A (PRKRA)	ENSP00000388455.1:n.*607T>A
ENST00000457633.2:c.*383T>A (PRKRA)	ENSP00000408668.2:n.*383T>A
ENST00000474793.6:n.1020T>A (PRKRA)
ENST00000676505.1:c.*639T>A (PRKRA)	ENSP00000504163.1:n.*639T>A
ENST00000676586.1:n.3016T>A (PRKRA)
ENST00000676752.1:n.2778T>A (PRKRA)
ENST00000676832.1:c.*700T>A (PRKRA)	ENSP00000503231.1:n.*700T>A
ENST00000676922.1:c.*607T>A (PRKRA)	ENSP00000503369.1:n.*607T>A
ENST00000677136.1:n.2871T>A (PRKRA)
ENST00000677206.1:c.*671T>A (PRKRA)	ENSP00000503034.1:n.*671T>A
ENST00000677253.1:c.*576T>A (PRKRA)	ENSP00000503466.1:n.*576T>A
ENST00000677386.1:c.*322T>A (PRKRA)	ENSP00000503003.1:n.*322T>A
ENST00000677460.1:c.*208T>A (PRKRA)	ENSP00000504507.1:n.*208T>A
ENST00000677584.1:c.*717T>A (PRKRA)	ENSP00000504411.1:n.*717T>A
ENST00000677689.1:c.624T>A (PRKRA)	ENSP00000502919.1:p.Asn208Lys
ENST00000677859.1:c.732T>A (PRKRA)
ENST00000677981.1:c.627T>A (PRKRA)	ENSP00000503536.1:p.Asn209Lys
ENST00000678053.1:c.*639T>A (PRKRA)	ENSP00000504330.1:n.*639T>A
ENST00000678058.1:c.623T>A (PRKRA)	ENSP00000503203.1:n.623T>A
ENST00000678167.1:c.*433T>A (PRKRA)	ENSP00000504479.1:n.*433T>A
ENST00000678775.1:c.540T>A (PRKRA)	ENSP00000504030.1:p.Asn180Lys
ENST00000678845.1:c.540T>A (PRKRA)	ENSP00000503011.1:p.Asn180Lys
ENST00000679037.1:c.*547T>A (PRKRA)	ENSP00000504421.1:n.*547T>A
ENST00000679202.1:n.1966T>A (PRKRA)
ENST00000325748.8:c.879T>A (PRKRA)	ENSP00000318176.4:p.Asn293Lys
ENST00000424699.5:c.*671T>A (PRKRA)	ENSP00000408029.1:n.*671T>A
ENST00000432031.6:c.846T>A (PRKRA)	ENSP00000393883.2:p.Asn282Lys
ENST00000487082.5:c.804T>A (PRKRA)	ENSP00000430604.1:p.Asn268Lys
ENST00000490501.5:n.1106T>A (PRKRA)
NM_001139517.1:c.846T>A (PRKRA)	NP_001132989.1:p.Asn282Lys
NM_001139518.1:c.804T>A (PRKRA)	NP_001132990.1:p.Asn268Lys
NM_001316362.1:c.540T>A (PRKRA)	NP_001303291.1:p.Asn180Lys
NM_003690.4:c.879T>A (PRKRA)	NP_003681.1:p.Asn293Lys
NR_110204.1:n.872-1222A>T (CHROMR)
NR_110205.1:n.716-1222A>T (CHROMR)
NR_110206.1:n.651-1222A>T (CHROMR)
XM_005246921.3:c.540T>A (PRKRA)	XP_005246978.1:p.Asn180Lys
XM_011512063.1:c.624T>A (PRKRA)	XP_011510365.1:p.Asn208Lys
XM_011512064.1:c.624T>A (PRKRA)	XP_011510366.1:p.Asn208Lys
XM_011512066.1:c.540T>A (PRKRA)	XP_011510368.1:p.Asn180Lys
XM_011512063.2:c.624T>A (PRKRA)	XP_011510365.1:p.Asn208Lys
XM_011512066.2:c.540T>A (PRKRA)	XP_011510368.1:p.Asn180Lys
XM_017005159.1:c.540T>A (PRKRA)	XP_016860648.1:p.Asn180Lys
XR_001739008.2:n.920T>A (PRKRA)
NM_003690.5:c.879T>A (PRKRA) MANE Select	NP_003681.1:p.Asn293Lys
NM_001316362.2:c.540T>A (PRKRA)	NP_001303291.1:p.Asn180Lys